Of all the elements known so far to be essential for health, iodine is the most misunderstood and the most feared. Yet, it is by far the safest of all the trace elements known to be essential for human health. It is the only trace element that can be ingested safely in amounts up to 100,000 times the RDA. For example, potassium iodide has been prescribed safely to pulmonary patients in daily amounts of up to 6.0 gm/day, in large groups of such patients for several years (1-3). It is important however to emphasize that this safety record only applies to inorganic nonradioactive iodine/iodide, not to organic iodine-containing drugs and to radioiodides. Unfortunately, the severe side effects of iodine-containing drugs have been attributed to inorganic iodine/iodide, even though published studies clearly demonstrate that it is the whole organic molecule that is cytotoxic, not the iodine covalently bound to this molecule. To quote Phillipou et al (4): “We can, therefore, conclude that the effect of amiodarone, benziodarone, Na iopanate and other iodine containing substances with similar effects is due to the entire molecule, and not to the iodine liberated. It should be noted that the cytotoxic effect of amiodarone in all cultures is also due to the entire molecule, and not to the iodine present in it.” Several forms of iodine are used in clinical medicine (Table I). Unless otherwise stated, this presentation is concerned only with inorganic nonradioactive iodine/iodide.
Medical iodophobia is the unwarranted fear of using and recommending inorganic nonradioactive iodine/iodide within the range known from the collective experience of three generations of clinicians to be the safest and most effective amounts for treating symptoms and signs of iodine/iodide deficiency (12.5-37.5 mg). This range of daily intake of this essential nutrient is thereafter referred to as orthoiodosupplementation, because it is the range of iodine/iodide intake required in order to achieve whole body sufficiency for this element based on a recently developed iodine/iodide loading test. (See Section VII for more details on the loading test).
Medicoiodophobes suffer from: A) Split personality which results in iodophobia within the orthoiodosupplementation range previously used safely and successfully in medical practice and iodophylia for megadoses of iodide (up to 12gm/day). B) Double standards, which render those physicians intolerant to the minor side effects of the inorganic forms and extremely tolerant toward severe side effects of the radioactive and organic forms. C) Amnesia toward the inorganic nonradioactive forms when making therapeutic decisions. D) Confusion, attributing the severe side effects of organic iodine containing drugs to inorganic iodine/iodide. E) Altered state of consciousness, allowing doublethink, doublespeak and contradictory logic to become acceptable. Although the factors involved in medical iodophobia are still unknown, decreased cognition seems involved. Since low iodine intake is associated with intellectual impairment, deficiency of this essential element cannot be ruled out, and if present, would create a self-perpetuating phenomenon. Needless to say that medical iodophobia is contagious and can be transmitted to patients and other physicians (iatrogenic iodophobia). Medical iodophobia will remain a syndrome until the causes are discovered and effective therapy implemented. It is very likely however, that medical iodophobia will eventually be classified as an iodine-deficiency disease.
Discovered in Imperial France (5), a century before the concept of essential trace element was proposed by Gabriel Bertrand (6); the first trace element tested in human subjects, and recognized as essential to human health (7,8), the most deficient trace element in the world (9), iodine had the misfortune of attracting the attention of endocrinologists because it is incorporated into some very important hormones of the thyroid gland (10-13). Starting out as a panacea for all human ills (14), iodine, as an essential element, became eventually associated exclusively with the thyroid gland (15). Thyroid fixation resulted in endocrinologists dictating the human needs for this nutrient. All human applications of iodine became eventually subservient to the dictates of misinformed endocrinologists.
For example, disinfection of water for human consumption and in swimming pools is far superior, safer, and less expensive with the use of iodine at 1 to 2 PPM, than with the use of chlorine and its derivatives at the same concentrations (16-19). However, unfounded concern about adverse effects of iodine at these levels on the thyroid gland (20-22 and vide infra), has prevented the widespread use of iodine for these applications, with toxic chlorine and its derivatives used by default. All studies published so far favor iodine over chlorine for treatment of municipal waters, and swimming pools: “Because of the increasing difficulty experienced by many communities in achieving satisfactory disinfection of public water supplies with acceptable concentrations of chlorine, a feasibility study on the use of iodine for this purpose was undertaken” (19). “The effectiveness, ease of administration and palatability were prime reasons for considering iodine as a disinfectant of community water supplies” (17). “effective bacteriological control of the water was maintained by all concentrations of iodine used in this study” (17). “At an iodine concentration of 1 mg/liter (1 ppm), the water met all standards for safety and palatability (1962 USPHS Drinking Water Standards)” (19). “During the five years in which this study was conducted no instances of urticaria or iodism were observed” (19). “No evidence of iodine-induced allergic phenomena was detected during this study” (17). “Comparative data indicate that disinfection of an Olympic-size swimming pool can be accomplished with iodine at half the dose of chlorination” (19). “Use of the iodinated swimming pool caused no significant changes in either the RAI uptakes or PBI concentrations” (19). The advantage of iodine over chlorine as a disinfectant in the treatment of municipal waters is that it could be used as a disinfectant and also as a source of a very important essential element. It is obvious that the benefits of such an approach would outweigh the risks, based on the studies mentioned above.
When different groups of competitive swimmers were asked about their preference between chlorine and iodine as a disinfectant of swimming pools (19), they overwhelmingly chose iodine. None preferred chlorine. “All members of the swimming teams of five universities who participated in AAWU swimming championships that were held in the Stanford pools were asked to express their opinions of iodine-treated water as compared with chlorine-treated water.” “Seventeen of the twenty freshmen and varsity swimming team members expressed a preference for the iodine-treated pool in respect to eye irritation. The other three had no preference, but none preferred the chlorine treatment. Of the championship swimming contestants 48 preferred the iodine-treated pool, 5 had no preference, but none preferred the chlorine-treated pool.” “Twenty-eight of the subjects who had been exposed to the iodine-treated water for 1 month were examined by the three physicians of the research staff, each of whom made his observations independently of the others. Twenty-seven of the swimmers examined received a completely negative rating for eye irritation. In only one student was a mild conjunctivitis found on medical examination. This student wears contact lenses and stated that his eye irritation had improved in a miraculous way since the pool had been treated with iodine.”
In the early 1960’s, iodine was added to bread as a dough conditioner. One slice of bread contained the full RDA of 150 ug (23,24). As would be expected because of isotope dilution effect, the percent of radioiodide uptake by the thyroid gland decreased from 20-30% to 10-20%. In 1965, London et al (25), from the National Institute of Health, evaluated the amount of iodine present in 32 bakery products from 12 different commercial bakeries. They reported that a typical diet contributed to approximately one mg of iodine per day and 726 ug came from bakery products. Concern was expressed over the inhibition of thyroid hormone synthesis in thyrotoxic patients at those levels of iodine. The last sentence of their publication read: “One milligram of iodine will suppress the uptake of radioactive iodine by the normal thyroid gland, probably by simple dilution of the dose, and may considerably reduce organic binding of iodine in the thyroid glands of thyrotoxic persons (7).” Reference 7 of their manuscript is a study published in 1949 by Stanley (26) one year after the Wolff-Chaikoff Effect was reported in rats (27). The first paragraph of Stanley’s manuscript stated the objective: “The interest of thyroidologists was recently aroused by the demonstration by Wolff and Chaikoff (1) that, with levels of serum iodide higher than 20 to 30 micrograms per cent, organic binding of iodine in the rat thyroid was inhibited. Extension of these observations to man was undertaken…”.
The interest of thyroidologists could not have been aroused so quickly by the publication of Wolff and Chaikoff in The Journal of Biological Chemistry (27), a journal involved in publishing research in the basic sciences, not clinical medicine. The thyroidologist with aroused interest was Stanley himself who obviously had insider’s information in order to publish his manuscript within a year following the Wolff-Chaikoff publication, considering the fact that it takes several months for the review process in peer review journals, and that it would have required several months for him to design and perform his experiments after reading the Wolff-Chaikoff paper. During the year Stanley published his “extension of the Wolff-Chaikoff Effect to man”, he co-authored a paper with Astwood on the use of goitrogens in the management of patients with Graves’ disease as an alternative to inorganic iodine/iodide. It is a strange coincidence that the investigators who authored the iodophobic publications, regarding the so-called inhibition of organic binding of radioactive iodide in the thyroid gland by the administration of inorganic nonradioactive iodide, were also involved in testing goitrogens in laboratory animals and in normal human subjects; and implementing the use of these goitrogens as an alternative to inorganic iodine/iodide in patients with Graves’ disease (See Section IV).
Stanley concluded: “Thus, the observations of Wolff and Chaikoff in the rat were extended to man.” However, Wolff (28) in a review published in 1969 stated, “The rarity of iodide goiter in the face of the extensive exposure of a great many patients to iodide has not been satisfactorily explained.” Without preconceived ideas, it is easily explained: inorganic nonradioactive iodine/iodide is safe. “The demonstration of the Wolff-Chaikoff Effect in man remains presumptive.” Amen! Several researchers erroneously concluded that the rapid decrease in serum thyroxine (T4) following oral ingestion of inorganic iodine/iodide in thyrotoxic patients was due to the Wolff-Chaikoff Effect, that is sustained inhibition of T4 synthesis. However, Wartofsky et al (29) in 1970 evaluated the effect of Lugol solution, administered at 5 drops (30 mg iodine/iodide) three times a day in 5 thyrotoxic patients. Following a well-designed protocol, they concluded, “It is concluded that the rapid decrease in T4 secretion induced by iodine is not the result of an acute sustained inhibition of T4 synthesis (The Wolff-Chaikoff Effect), but rather results from an abrupt decrease in the fractional rate of thyroid T4 release”. Therefore, in hyperthyroidism, iodine/iodide in Lugol at a daily dose of 90 mg induced a physiological trend toward normalization of thyroid function, a beneficial effect.
One can appreciate the thyroid fixation of confused endocrinologists who ignore the rest of the human body in favor of misinterpreted laboratory tests assessing thyroid function. The concern about decreased uptake of radioiodide by the thyroid gland following ingestion of increasing amounts of inorganic nonradioactive iodide shows lack of understanding of the physiological interpretation of the iodide tracer. Theoretically, as we previously discussed (30), the uptake of radioactive iodide by the thyroid gland should be zero in order to achieve sufficiency of the thyroid for inorganic nonradioactive iodide. Decreased thyroid uptake of inorganic radioiodide is an effect to be desired, not avoided. Besides, a low radioiodide uptake by the thyroid resulting from adequate intake of inorganic non-radioactive iodine/iodide (orthoiodosupplementation) serves as a preventive measure against unexpected exposure to radioactive iodide/iodine (30). Based on a review of the literature, we computed the daily amount of iodine/iodide needed for sufficiency of the thyroid gland and the whole human body. This amount, called orthoiodosupplementation, amounted to 100 times the RDA (30).
In the 1980’s, thanks to iodophobia, iodine was replaced with bromine in the bread making process (31). Bromide is a goitrogen and interferes with iodide utilization by the thyroid gland (32-34), and possibly by the mammary gland also (35). Iodine has an anticarcinogenic effect on the breast (30). The last national nutritional survey showed a trend of decreasing iodine intake by the U.S. population (30,31). Currently 15% of the U.S. adult female population excreted in their urine less than 0.05 mg iodide/L, a level classified by the World Health Organization (WHO) as iodine deficiency. One must keep in mind that the amounts of daily intake of iodine set by the WHO, were recommended with the goal of preventing simple goiter and stupidity (cretinism), not for sufficiency of the whole human body for iodine, an amount we estimated to be 100 fold higher than the recommended daily intake (30). Concurrent with the decreased intake of iodine/iodide and increased intake of bromine in the U.S. population, a trend of increasing prevalence of cancers of the mammary and thyroid glands was reported (30).
Velicky et al (33), in a 1997 publication, reported that rats consuming low levels of bromide, similar to levels presently consumed by human subjects, developed goiter, even though those rats received the normal amount of iodide in their diet. Under histological examinations, increased mitotic activity of the follicular epithelium was observed. The values of the mitotic index increased with increasing intake of bromide. The authors discussing their results, commented: “This finding is important in connection with the data showing an increasing exposure of living organisms to environmental bromine which represents an important environmental factor contributing to the development of endemic goiter; this is caused by a decreased utilization of the consumed iodine which produces a relative iodine deficiency even when the iodine intake is sufficient.” “The transport of iodine and its organification can be blocked by Br- ions due to a mutual competition between bromide and iodide anions… This results in a thyroxin and triiodothyronine deficiency, which in turn increases secretion of TSH.” “Each stimulation of cell proliferation is obviously a key factor in the tumor growth of the thyroid (Williams, 1992) and an increased incidence of thyroid carcinoma in humans is higher in regions with iodine deficiency (Gaitan et al, 1991).”Shimomura et al (36) observed that bromine enhances the biological activity of a tumor promoter. Sangster et al (37) reported a decreased ability to concentrate and sleepiness in normal male subjects ingesting 4 mg sodium bromide/Kg BW/day. This hypnotic effect could be due to oxidation and organification of bromide in the central nervous system. Torii et al (38) tested an organic bromine compound, isolated from the cerebrospinal fluid of patients with bromism. In cats, this organic bromine induced REM sleep. Therefore, bromine has a zombifying potential. Why iodine was replaced with a goitrogen possessing carcinogenic and zombifying potentials in a population already very iodine deficient even by the very low RDA standard, remains a mystery!! Nevertheless, it is a very effective way to keep a nation sick and zombified.
The purpose of this manuscript is to review studies published during the late 1800’s and early 1900’s describing the effect of oral ingestion of inorganic nonradioactive iodine/iodide in patients with simple goiter, and in Graves’ disease, both conditions due to iodine/iodide deficiency. This physiological approach will be compared with the current nonphysiological trend of prescribing to iodine deficient female patients with hypothyroidism and simple goiter the hormone thyroxine (T4), which increases the risk of breast cancer in those patients (discussed in Section III). In Graves’ disease, the nonphysiological use of goitrogens and radioiodide has replaced iodine/iodide resulting in hypothyroidism of these unfortunate patients. It seems that no matter what your thyroid problem is, you always end up getting T4. In the discussion of published data on iodine-induced hypothyroidism and hyperthyroidism, a clear distinction will be made between inorganic versus organic forms, in order to demonstrate that adverse effects attributed to iodine in most publications, were the result of ingestion and injection of organic forms of iodine-containing drugs. A review of some historical events combined with some physiological aspects of iodide metabolism by the thyroid gland will be discussed in order to demonstrate that inadequate iodine/iodide intake combined with goitrogens, not excess iodide, is the cause of autoimmune thyroiditis. Last, the concept of orthoiodosupplementation will be presented, including the description of a simple iodine/iodide loading test to assess sufficiency of the whole human body. Orthoiodosupplementation is the safest and most effective method of supplementing patients with this essential trace element in amounts for whole body sufficiency.
II. The discovery of iodine
The discovery of the stable halides, chloride, iodide, bromide and fluoride seems to have been a French enterprise. All 4 halides were identified by French scientists, (Table II) with H. Davy from Great Britain, sharing the discovery of chloride with Gay-Lussac in 1809-1810 (39).
Bernard Courtois, a French chemist, was a saltpeter (potassium nitrate) manufacturer. Saltpeter was one of the compounds needed for the manufacture of gunpowder. Seaweed ash was used as a valuable source of sodium and potassium salts. Sulfuric acid was added to remove interfering compounds before the salts could be precipitated. One day toward the end of AD 1811, Courtois added too much acid to the suspension of seaweed ash. The iodides in seaweed were oxidized to iodine, which sublimated and formed a violet vapor above the preparation. The crystals obtained from condensation of the iodine vapor were analyzed by Courtois and he prepared several iodide salts. Courtois never published his findings. Some of these crystals ended up in the hands of Gay-Lussac and Ampere who gave some to H. Davy. An anonymous paper was published in 1813, written by Gay-Lussac, giving full credit to Courtois for the discovery of iodine (5). In the same year, C.B. Desormes and N. Clement presented Courtois’ discovery at a meeting of the Imperial Institute of France. Gay-Lussac named the new element “iode” from the Greek ioeides meaning “violet-colored”. H. Davy anglicized the name iode and called it iodin, which became iodine in the 1930’s.
By 1813, Gay-Lussac had synthesized several products from iodine and fully characterized this new element, but he gave full credit to Courtois for the discovery of iodine. According to the Dictionary of Scientific Discovery (39), Davy, in an attempt to eclipse Gay-Lussac in the characterization of iodine, did the unthinkable for a scientist of his rank: “A large part of Davy’s claim for the originality of his study of iodine depends on his complete honesty in claiming certain knowledge before that of Gay-Lussac and in particular in dating as 11 December a paper read to the Institute on 13 December (that is the day following Gay-Lussac’s publication)”. Courtois did not benefit from his discovery. “… in 1831 the Institute awarded him a prize of 6,000 francs for the discovery. By this time Courtois had given up the saltpeter business and, from the 1820’s, attempted to make a living by preparing and selling iodine and iodine compounds. This enterprise also failed, and he died in poverty.” (39)
The history of iodine in medicine and pharmacy was reviewed by F.C. Kelly (14) from its discovery in 1811 up to 1961. The review of the history of iodine by L.E. Braverman (15), covering the period from 1961 to 1994, was limited to the thyroid gland exclusively, because, by then thyroid fixation had become pandemic and the only role of iodine as an essential element was assumed to be due to its incorporation in the thyroid hormones. Detailed information about the intrigue and the political climate may be found in the Dictionary of Scientific Biography (39) edited by C.C. Gillispie and published in 14 volumes by Simon and Schuster, New York, N.Y. (1970). The scientists are listed alphabetically with their accomplishments.
III. The use of inorganic nonradioactive iodine/iodide in simple goiter
Centuries before the discovery of iodine, seaweed was used in the treatment of thyroid enlargement (goiter). In his review, F.C. Kelly (14) mentioned Chinese physician Ke-Hung (AD 281-361) who used seaweed in the treatment of goiter. Five centuries later, Wang Tao listed 36 prescriptions for goiter, 27 of which contained seaweed. The name “thyroid” was assigned to this gland by British physician Thomas Wharton in his book Adenographia, written in Latin and published by himself in 1656 (39). The goal of this book was “a description of the glands of the entire body”. The name thyroid (shield) was assigned to the gland because the thyroid cartilage behind the gland was in the shape of a shield. Wharton postulated that the role of the gland was purely esthetical. He observed that the thyroid was larger in women than in men: “It (the thyroid gland) contributes much to the beauty of the neck… particularly in females, for this reason, a larger gland has been assigned, which renders their necks… more beautiful.”
After the discovery of iodine from seaweed, a Swiss physician, J.F. Coindet who previously used successfully burnt sponge and seaweed for goiter, reasoned that iodine could be the active ingredient in seaweed. In 1819, he tested tincture of iodine at 250 mg/day, an excessive amount by today’s standard, in 150 goiter patients with great success. He could reduce significantly the size of goiter within a week. He published his results in 1820 (40). He later reported some side effects to iodine, including iodine-induced thyrotoxicosis (41). “I have observed goitrous patients who have been greatly affected by the treatment: acceleration of the pulse, palpitations, dry frequent cough, insomnia, rapid emaciation, loss of strength, in others only swelling of the legs or tremor of a painful hardening of the goiter, sometimes a shrinkage of the breast, remarkable and sustained increase in appetite.” He was the first physician to use iodine in medical practice. To be discussed later, the use of combined inorganic iodine/iodide (Lugol solution) in the right amounts resulted in better response with less complications than iodine and iodide alone.
Because iodine is not very soluble in water, (330 mg/Liter), alcoholic tinctures were first used externally as an antiseptic and internally as a treatment for every conceivable medical and surgical condition. In 1829, Jean Lugol, a French physician researching the medical uses of iodine in infectious diseases (42), observed that the presence of potassium iodide in water increases markedly the aqueous solubility of iodine, from 0.33 gm/L to 50 gm/L. The Lugol solution contains 5% iodine and 10% potassium iodide in water. He used his preparation for the treatment of “les maladies scrofuleuses.” The antiseptic properties of iodine were widely used from the discovery of iodine until today. In 1873, French bacteriologist Davaine used tincture of iodine as an agent to treat anthrax in patients suffering from this infection (39). Orthoiodosupplementation (30) may be the best preventive measure against bioterrorism. It is important to point out that iodides have no antiseptic and antibacterial properties. Only iodine, the oxidized state, is antiseptic. Since iodine is not very soluble in water, the best preparation of an aqueous solution of iodine is Lugol solution because it allows the administration of relatively large amount of iodine in small volumes of water. The collective experience of a large number of clinicians over the last century has resulted in the recommended daily amount of 0.1 to 0.3 ml of Lugol, containing from 12.5 to 37.5 mg elemental iodine, for iodine/iodide supplementation. Interestingly, this is the range of iodine/iodide intake required for whole body sufficiency based on a recently developed iodine/iodide loading test, discussed in Section VII. We have confirmed the observations of our medical predecessors who were keen observers.j
In 1831, French chemist and agronomist J.G. Boussingault (43) proposed iodized sodium chloride (table salt) as a mean of preventing goiter. Such proposal was implemented first in Europe and then in the 1920’s, in the USA. That was a very bad idea because it gave a false sense of iodine sufficiency and resulted in the public relying on iodized salt for supplementation instead of the previously used forms of iodine and iodide such as the Lugol solution. In order to ingest 12.5 mg of elemental iodine from salt, one would have to consume 165 gm of salt; and obviously 3 times that amount of salt would be required for supplying 37.5 mg elemental iodine. Beside, table salt contains iodide only, not iodine. To be discussed later, iodine is very important for normal function of breast tissue. Therefore, supplementation should contain both forms, iodine and iodide.
In 1926, physician C.L. Hartsock, from Cleveland, Ohio, (44) wrote: “…iodized salt is now being very much more extensively used by the public than other forms of iodine, such as sodium iodide, iodostarine and compound solution of iodine (Lugol’s solution), probably because of the propaganda to insure its use…”. Iodized salt was unfortunately used as substitute for the previously recommended forms of iodine/iodide. The average daily intake of iodide from iodized salt represents less than 1% of the recommended daily intake of Lugol solution. Implementation of iodization of salt was associated with an increased incidence of autoimmune thyroiditis. In section VI of this manuscript, we will propose a mechanism that could explain how inadequate iodide intake combined with goitrogens in a previously iodine-deficient individual caused oxidative damage to thyroid peroxydase and thyroglobulin, resulting in an autoimmune reaction to those proteins. The same mechanism can explain autoimmune thyrotoxicosis (Graves’ disease). Hartsock recommended the use of a tablet of iodine/iodide in known and fixed amounts as the best form of supplementation, just like the most popular form of supplementation used today for vitamins, minerals and trace elements. “Tablets containing definite amounts of iodine seemed to be the method of choice.”
Following Coindet’s original success in treating goiter with tincture of iodine in 1819 and 1820, “In the first flush of enthusiasm for the newcomer, physicians and surgeons tested it and tried it for every conceivable pathological condition.” (14). However, no attempt was made to study the optimal daily requirement of the human body for iodine, because the concept of “essential trace element” was not proposed until the end of the nineteenth century by Gabriel Bertrand (6). Even after iodine was recognized as an essential element in the 1920’s, mainly due to Marine’s studies (7,8), no attempt was made to assess the optimal daily requirement of this nutrient for sufficiency of the whole human body. Marine (8) used a daily average of 9 mg iodide in the prevention of goiter in adolescent girls, an amount 60 times the current RDA for iodine. In 1930, Thompson et al (45) stated: “The normal daily requirement of the body for iodine has never been determined.” This statement is still true today, more than 70 years later. We still don’t know the iodine/iodide requirements for whole body sufficiency.
In 1821, Francois Magendie was the first to put iodine into a pharmacopoeia (14). The number of preparations containing iodine and iodine compounds increased rapidly afterward. To quote Kelly: “In the Great Exhibition at the Crystal Palace in Hyde Park in May 1851 iodine and iodine compounds were publicly shown for the first time by ten pharmaceutical firms, …” “…by 1890, to choose a date at random, the 6th edition of Martindale’s Extra Pharmacopoeia sponsored 30 medicaments derived from iodine; the ‘Iodine Centenary Volume’ compiled by ‘The Prescriber’ in 1914 mentions 45 iodine preparations; by 1928 ‘Martindale’ had extended its coverage to 128 iodine items: and, in an International Index published in 1956, and devoted exclusively to iodine pharmaceuticals, no less than 1,700 approved pharmacopoeial names, proprietary names, synonyms, and alternative designations are alphabetically listed.”
As late as 1995, the 19th Edition of Remington’s Science and Practice of Pharmacy (46), continued to recommend between 0.1 to 0.3 ml daily of Lugol 5% solution in the treatment of iodine deficiency and simple goiter. The 5% Lugol solution contains 50 mg iodine and 100 mg potassium iodide per ml with a total of 125 mg elemental iodine/ml. The suggested daily amount of 0.1 ml to 0.3 ml is equivalent to 12.5 mg to 37.5 mg, with 40% iodine and 60% iodide as the potassium salt (orthoiodosupplementation). This amount was based on the collective experience of clinicians over the last century. We have recently confirmed the keen observation of our medical predecessors. The range of Lugol solution they recommended is exactly the range of iodine/iodide intake for whole body sufficiency based on a recently developed iodine/iodide loading test (discussed in Section VII). In the early 1920’s the influence of Plummer increased further the popularity of Lugol solution among clinicians. In 1932, physician B.N. Cohn (47) wrote: “…the widespread use of compound solution of iodine, U.S.P., (For the reader’s information, that is Lugol solution) is the result of a paper by Plummer and Boothby, published in that year (1923). Since then compound solution of iodine has been used by nearly every clinician ...”
With the availability of thyroid extracts in the early 1900’s, and thyroid hormones in the 1930’s, thyroidologists started using these preparations in patients with iodine deficiency and simple goiter instead of the previously used inorganic iodine/iodide preparations. The situation was aggravated in the 1930’s by the fact that during the same period, the public was relying on iodized table salt instead of iodine/iodide preparations from apothecaries for supplementation, due to the propaganda favoring the use of iodized salt (44). The thyroidologists assumed that, with iodization of table salt, iodine deficiency became a thing of the past, because of the positive effect of iodized salt on the incidence of goiter. That was the beginning of thyroid fixation. Most physicians, by the 1950’s neglected the rest of the human body, in terms of sufficiency for iodine, and forgot that their predecessors were using amounts of iodine/iodide 2 orders of magnitude greater than the amounts present in the average daily consumption of table salt. This was mainly due to iodophobic publications appearing in the mid 1940’s (discussed in Section IV) and also due to the erroneous assumption that absence of goiter means iodine sufficiency. A textbook entitled “Diagnosis and Treatment of Diseases of the Thyroid”, edited by Amy Rowland and published in 1932, contained chapters from 24 thyroidologists of that time (48). Although the most common cause of hypothyroidism and simple goiter worldwide is iodine deficiency, the recommended treatment of hypothyroidism was summarized in 2 sentences: “The treatment of hypothyroidism of any type consists merely in the substitution of thyroid extract for the deficient secretion. Any form of prepared gland or the active principle, thyroxin, may be used.” However, not all physicians abandoned iodine/iodide and many continued up to the present day to use Lugol solution and potassium iodide in the treatment of iodine deficiency and simple goiter. Today, this is called alternative medicine but 100 years ago, it was mainstream medicine. In 1921, S.P. Beebe stated: “We may say that medical treatment of simple goiter is contained in this one word – iodine.” (49).
It is unfortunate that mainstream endocrinologists today do not share Beebe’s enthusiasm for iodine. In the 8th Edition of The Thyroid published in 2000, Brent and Larsen (50) wrote the chapter on the treatment of hypothyroidism in the adult. They stated: “The goal of treatment of hypothyroidism is to normalize thyroid status in peripheral tissues, whatever the cause of the hypothyroidism. The usual approach is to give sufficient T4 to ameliorate all symptoms of hypothyroidism and, in patients with primary hypothyroidism, to reduce serum TSH concentrations to within the normal range…”. In the battle royal for supremacy, T4 became the uncontested winner in the treatment of simple goiter and hypothyroidism, caused by iodine deficiency and goitrogens, but the female patients became the real losers with increasing prevalence of obesity, diabetes, hypertension; and cancers of the breast and thyroid glands (30). What happened to inorganic nonradioactive iodine/iodide?? Don’t they know that iodine deficiency in women predisposed them to breast cancer (30), and that giving T4 to iodine-deficient women increases further their risk for breast cancer (51)?
IV. The use of inorganic nonradioactive iodine/iodide in Graves’ disease
Since Graves’ disease represents up to 90% of hyperthyroidism (52), we will limit our discussion to Graves’ disease, called by different names in different publications: exophthalmic goiter, or goitre, hyperthyroidism; and toxic goiter.
Iodine was used in the treatment of toxic goiter as early as 1840 by Von Basedow (53) and in 1854 by Stokes (54). In 1863, Trousseau inadvertently used tincture of iodine successfully in a patient with exophthalmic goiter (55). “In the course of October, 1863, I was consulted by a young married lady, who habitually resides in Paris. She was suffering from subacute exophthalmic goiter. …I still found her heart beat at the rate of 140 to 150 times in the minute… I wished to administer at the same time tincture of digitalis, but preoccupied with the idea that there would be some danger in giving iodin, I wrote iodin instead of digitalis, so that the patient took from 15 to 20 drops of tincture of iodin a day for a fortnight. (For the reader’s information, “tincture of iodin” is a 10% solution of iodine in 95% ethanol. The daily amount ingested was 75-100 mg). When she then came back to me, her pulse was only 90. I found out my mistake, and I substituted tincture of digitalis for that of iodin, but, after another fortnight, the pulse had again gone up to 150, so that I at once returned to the iodin.” Trousseau had the distinction of performing the first double blind study of iodine in a cohort of one patient with Graves’ disease. He also achieved remission of Graves’ disease with prolonged administration of potassium iodide (56). Thompson et al (57) in a 1930 publication, quoted several authors in the late 1800’s and early 1900’s who used Lugol solution alone successfully in Graves’ disease, with complete remission of the disease, eliminating the need for surgery. Destruction of the thyroid gland with goitrogens and radioiodide was fortunately not then available for the management of Graves’ disease. Professor Kocher came on the scene in the early 1900’s and had an adverse iodophobic effect on the treatment of Graves’ disease. Professor Theodore Kocher carried a lot of weight, being the recipient of the Nobel Prize in Medicine and Physiology in 1909 for his work on “thyroid surgery”, the only Nobel Prize assigned to research on the thyroid gland. He was against the use of iodine/iodide in exophthalmic goiter and all forms of hyperthyroidism (58,59).
Cowell and Mellanby in their 1925 publication (60) gives up a glimpse of Kocher’s influence over the thyroidologists of that time, bordering on intimidation: “Kocher taught that the administration of potassium iodide must never be carried out in exophthalmic goiter, and on the whole, this advice has been taken. As evidence of this fact may be mentioned the discussion on the treatment of exophthalmic goiter at the Royal Society of Medicine in 1923. No speaker mentioned iodine or any preparation of iodine as being of any value in the treatment of the disease, and it can be inferred that therapy involving the use of iodine has been deliberately avoided.”
The influence of Kocher divided thyroidologists into 2 schools: the iodine/iodide school which favored the use of Lugol solution first and then adding surgery later for the patients not responding to this approach alone, while continuing the iodine/iodide supplementation. The surgical school discouraged the use of iodine/iodide, prior to and post surgery. DeCourcy (61) in 1927 stated: “That the administration of iodine prior to operation for exophthalmic goiter controls the symptoms, lowers the basal metabolic rate and lessens the hazards of operation, is no longer questioned. This teaching, however, is directly contrary to that of only a few years ago. Formerly the surgical school led by Kocher opposed the use of iodine in any form of Graves’ disease, holding that it increases the severity of the symptoms and may, in fact, be responsible for the development of exophthalmic from simple goiter.” In the same publication, DeCourcy’s own experience revealed that out of 30 cases of exophthalmic goiter in children, Lugol solution 5-10 drops (30-60 mg) three times a day “made operation unnecessary” in 11 cases. That is a 36% success rate.
Some brave souls defied Kocher’s moratorium and continued to use inorganic iodine/iodide successfully in Graves’ disease. Retrospectively, Kocher’s stand against inorganic iodine/iodide in Graves’ disease proved to be the main cause of the high rate of pre- and post-operative mortality, following thyroidectomy. In 1924, Plummer and Boothby from the Mayo Clinic (62,63) reported their experience with 600 cases of Graves’ disease, who received Lugol solution for several days pre-operatively and post-operatively, resulting in zero medical mortality: “In the Mayo clinic we now give 10 minims of Lugol’s solution as a routine three times a day for at least seven days previous to a thyroidectomy. (For the reader’s information, one minim is one drop of Lugol, containing 6.25 mg of total elemental iodine. The daily amount was about 180 mg). The solution is administered for a longer period to patients who have been in a particularly bad condition, and are at the end of this period rapidly improving. To patients in a crisis or near-crisis, 50 minims are given during the first two or three hours, by mouth if it can be retained, otherwise by rectum. If the patient is in a crisis, this is followed by 50 minims during the following forenoon. To the patients having so-called postoperative recurrences that can be controlled are given 10 minims of the solution daily over an indefinite period. This period is generally determined by stopping the iodin at intervals of a few weeks, and noting the patient’s condition at the end of ten days. If there is any recurrence of hyperthyroidism, the administration of iodine is again resumed.” “From January 1 to September 1, 1924, from 600 to 700 new cases of exophthalmic goiter were observed in the Clinic. During this period there were no medical death.”
In 1925, Frank H. Lahey (64) from the Lahey Clinic in Boston reported his experience with Lugol solution in Graves’ disease. “The introduction of Lugol’s Solution by Dr. Henry S. Plummer as a method of preparation for operation in exophthalmic goiter marks a step of forward progress in the surgical management of this disease. It has practically eliminated preliminary pole ligation in our Clinic and has made it possible to complete the operation of subtotal thyroidectomy in one stage upon a great majority of our patients. It has saved for us many of those delirious and desperately toxic cases which previously died before any operation could be done upon them, and it has almost completely done away with post-operative thyroid reactions. It has been a real boon to the patient suffering from exophthalmic goiter or primary hyperthyroidism.”
Thompson et al (57) published the results obtained in 24 patients with exophthalmic goiter treated with Lugol solution alone without surgery, using a daily dose of one drop. As mentioned previously, goitrogens and radioiodide were not available for use in Graves’ disease until the mid 1940’s, coincident with the appearance of iodophobic publications by the same authors who promoted the goitrogens as an alternative to Lugol solution in the management of Graves’ disease. Thompson et al stated: “Twenty-four patients with exophthalmic goiter (fourteen mild and ten severe or moderately severe cases) have been treated in this clinic with iodine alone, either continuously or intermittently for periods ranging from one and one-half months to three years. The period of treatment was a year or more in thirteen instances. With three exceptions (all unsatisfactory responses to iodine) the patients pursued their daily work throughout the period of observation, thus eliminating the effect of rest.” That is an 88% success rate.
S.P. Beebe from New York reported favorably in 1921 on the use of Lugol solution in hyperthyroid forms of goiter (49), based on his experience over a period of 10 years, which did not confirm Kocher’s iodophobic attitude: “In going over these statements in the literature it seems probable that the actual basis for the conclusions has been theoretical considerations and preconceived notions rather than careful clinical observations.” “In the writer’s experience iodine is one of the most valuable therapeutic agents we have in the treatment of the hyperthyroid forms of goiter. As in the case of any potent drug, injury can be done with it. So can we do injury with digitalis and salvarsan. During the last ten years the writer has treated a large number of cases of hyperthyroidism, and with most of them the administration of iodine has been a part of the treatment. There is no danger in so doing if the dose is properly regulated. The extreme sensitiveness described by some writers is a rare event. If the dose is properly regulated there need be no fear of iodism or iodine Basedowism.”
Starr et al (65) from the Massachusetts General Hospital used 15 drops (90 mg) of Lugol daily for the treatment of exophthalmic goiter, with a 92% success rate, eliminating the need for surgery. “Of these twenty-five cases, twenty (80 per cent.) responded to iodin by a more or less extensive remission of the disease. Of these twenty, twelve (48 per cent.) responded with the acute iodine remission resembling the effect produced by subtotal thyroidectomy. In the remaining eight (32 per cent.) the remission occurred, but was less extensive. In five unsuccessful cases (20 per cent.) two of the patients were pregnant and one had cardiac decompensation. If these are omitted from the calculation, iodine administration was successful in twenty of twenty-three, or 92 per cent. of our hospital cases.”
A cursory review of the literature suggests that the use of Lugol solution in Graves’ disease, the preferred approach by thyroidologists of that time, resulted in a higher success rate with fewer complications than the use of iodine and iodide alone (45,57,60-66). The daily amount of Lugol solution used in Graves’ disease ranged from one drop (6.25 mg) to 30 drops (180 mg). A complete nutritional program in our experience improved further the response to orthoiodosupplementation in Graves’ disease and other thyroid disorders.
No serious attempt was made by physicians of the early 1900’s to incorporate a complete nutritional program with Lugol supplementation in the management of thyroid disorders. The reason is that not much was know about the vitamins, minerals and essential trace elements at that time. Today, the importance of good nutrition in overall wellbeing is commonly accepted and more and more publications are emphasizing the interaction between micronutrients in their overall effects on biological systems. We have incorporated a total nutritional program with orthoiodosupplementation, emphasizing magnesium instead of calcium (discussed further in Section VII). The effect of this nutritional program with orthoiodosupplementation on thyroid function tests in a 40 year old female patient with severe hyperthyroidism is displayed in Table III.
She was a classic case of Graves’ disease with exophthalmia. After researching the medical literature, she refused treatment with radioiodides, goitrogens and surgery. She was placed on the nutritional program, including 1200 mg of magnesium/day for one month prior to iodine supplementation, followed by the same program with the addition of 12.5 mg elemental iodine (1 tablet Iodoral®) daily afterward. TSH was undetectable at <0.01 uU/ml. Total T4 was 18 ug/dL; total T3 442 ng/dL; free T4 = 5 ng/dL. Following one month on a high magnesium program, she stated she felt calmer, with less palpitation; could sleep better. The burning, irritation and lacrimation of the eyes improved. TSH remained undetectable at 0.03 uU/ml; total T4 dropped to 16 ug/dL and total T3 from 442 to 299 ng/dL. Free T4 did not change appreciably. After the first week on iodine/iodide at 12.5 mg/day, she noticed a clearer mind with improved cognition. Following one month on this program, she slept better and was better organized with improved social activities. Her palpitation decreased markedly with normal pulse rates. Serum TSH became normal at 2.3 uU/ml; total T4, total T3 and free T4 were all within the normal range at 8.0 ug/dL; 195 ng/dL; and 1.2 ng/dL. She continued to improve. After 3 months on the same program, TSH was not measured, but total T4, Total T3 and free T4 remained within the normal range (Table III). She experienced some diarrhea following 4 months on magnesium at 1200 ug/day and the daily amount was decreased to 600 mg/day. As of this writing, the thyroid function tests remained within the normal range; she has no exophthalmia; she gained 16 lbs., and her social activities have improved to the point of matrimony. She praises God every day for saving her thyroid gland and making her healthy again.
Published studies on the safe and effective use of Lugol solution in Graves’ disease mysteriously disappeared during the 1940’s and afterward, concurrent with the appearance of iodophobic publications, and the promotion of goitrogens as an alternative to Lugol solution in the management of Graves’ disease. (Table IV). Introduced in 1943 by E.B. Astwood (67) for the management of Graves’ disease in the forms of thiourea and thiouracil, these goitrogens evolved into more powerful ones (68), and eventually the thionamides: methimazole, carbimazole and propylthiouracil. These goitrogens rapidly replaced inorganic iodine/iodide in the management of Graves’ disease. The synchronization of iodophobic publications with the introduction of goitrogens to replace inorganic iodine/iodide (Table IV) was a brilliant move and it worked wonderfully. Obviously, no one was awake to ask questions. In 1953, when Godley and Stanbury (69) introduced a new goitrogen, potassium perchlorate, in the treatment of hyperthyroidism, they acknowledged that the thiionamides were used widely in Graves’ disease, instead of inorganic iodine/iodide. “At the present time propylthiouracil, methylthiouracil and 1-methyl-2mercaptoimidazole (methimazole) are widely employed in the preparation of thyrotoxic patients for surgery, and to a lesser extent in the chronic control of the overactive thyroid gland (5).” This new goitrogen, that is potassium perchlorate, was so toxic that it was removed from circulation shortly after its introduction. Reintroduction of this goitrogen is currently being attempted by lowering the recommended dosage (70).
Astwood and his associates reported very high remission rates in Graves’ disease with the use of goitrogens, which mislead thyroidologists and encouraged them to use these drugs instead of inorganic iodine/iodide. In two studies published in 1953 and 1966, his teams reported remission rate of 50-75% (71,72). However, his findings could not be reproduced by others. Wartofsky (73) in 1973, and Reynolds and Kotchen in 1979 (74) observed much lower remission rates of 11-16%. Increased ingestion of iodine/iodide by the patients was blamed by Wartofsky for the low success rate. Wartofsky’s study was done at a time when one slice of bread contained the full RDA for iodine. In an attempt to improve success rate with goitrogens, patients were told to limit their intake of iodine, which discouraged further its use by the patients. Wartofsky et al (73) failed to realize that iodization of bakery products started several years before the second study by Astwood et al (72) published in 1966, which reported a very high success rate. In 1965, London et al (25) reported an estimated iodine intake of 1 mg/day with 726 ug coming from bakery products. In the end, one would have to conclude that Astwood’s optimistic reports on the use of goitrogens in Graves’ disease could not be reproduced by others. Since the word “goitrogens” implies goiter-causing drugs, Astwood called them antithyroid drugs. So, instead of normalizing thyroid function physiologically with sufficient amounts of inorganic nonradioactive iodine/iodide, thyroidologists became destructive in their approach with goitrogens and radioiodide, resulting in hypothyroidism in the majority of those unfortunate patients who eventually join the ever increasing T4 consuming population.
In the 1980’s, thyroidologists in the USA decreased their use of goitrogens in Graves’ disease due to low remission rate and side effects and relied more and more on inorganic iodide, but unfortunately the wrong kind, the radioactive kind, that is. Thyroidologists en masse joined the nuclear age. In 1990, a survey by the American Thyroid Association (75) revealed that the majority of their members relied on radioiodide predominantly, with the exception of the very young and the pregnant, whom the compassionate thyroidologists protected by giving them goitrogens!! Only 2% opted for surgery; 28% used goitrogens and 70% joined the nuclear age. There was no mention of inorganic nonradioactive iodine/iodide as an option. In the last edition of Werner and Ingbar’s The Thyroid published in AD 2000, D.S. Cooper wrote the chapter on treatment of thyrotoxicosis (76): “This chapter considers the three forms of treatment of thyrotoxicosis – antithyroid drugs, radioactive iodine (radioiodine), and thyroidectomy – that are in wide use now.” In a subsection entitled “Other drugs used in the treatment of thyrotoxicosis caused by Graves’ disease”, Cooper stated “The effects of iodide on thyroid function are complex and are discussed in detail in the section on the effects of excess iodide in Chapter 13.” The reader is preconditioned to be in an iodophobic mode when he goes to Chapter 13, an ominous number, with the title “…excess iodide…” and, where inorganic iodine/iodide is blamed for the severe side effects of organic iodine containing drugs such as amiodarone, and is called “A pathogen”.
Obviously, the unsuspecting thyroidologist relying solely on this textbook for information will avoid inorganic iodine/iodide like leprosy. If he is inquisitive however, and searches the literature carefully, he may read the publication by Phillipou et al (4) who studied the effect of inorganic iodide on thyroid functions and compared his results with the effects of amiodarone: “We can, therefore, conclude that the effect of amiodarone, benziodarone, Na iopanate and other iodine containing substances with similar effects is due to the entire molecule, and not to the iodine liberated. It should be noted that the cytotoxic effect of amiodarone in all cultures is also due to the entire molecule, and not to the iodine present in it.” It is most amazing that no one so far has proposed the use of inorganic nonradioactive iodine/iodide at 9 mg/day in patients with cardiac arrhythmia. Indeed, we have a zombified medical profession. A case in point: Patients are told to protect their thyroid gland from radioactive fallout by ingesting inorganic nonradioactive iodide. However, the same patients, if diagnosed with Graves’ disease, are told to stop taking inorganic nonradioactive iodine/iodide in order to allow the largest concentration of radioactive iodide to penetrate their thyroid gland, a destructive dose that is!! Does that make any sense??
V. Hypo- and hyperthyroidism caused by organic and inorganic forms of stable iodine/iodide
A critical evaluation of some review articles on iodine-induced hypothyroidism and iodine-induced hyperthyroidism reveals that in most cases, organic forms of iodine are involved. However, the titles of those articles suggest that the review is about inorganic iodine/iodide. For example, in the latest published review on “iodine-induced hypothyroidism” by Markou et al in 2001 (77), the list of iodine-containing products causing hypothyroidism consisted predominantly of organic forms of iodine such as amiodarone and radiology contrast agents. The title of that review should be “Drug-induced hypothyroidism”. In 1984, Leger et al (78) reported 85 cases of “iodine-induced thyrotoxicosis”. Amiodarone alone accounted for 50% of the cases. All the patients received organic forms of iodine containing drugs. The title of that review should be “Drug-induced hyperthyroidism”.
In 1983, Fradkin and Wolff (79) published a review on “iodide-induced thyrotoxicosis”. Since organic forms contain iodine, not iodide, using “iodide” in the title implies we are dealing with the inorganic forms. However, in the first paragraph of that review, we read: “Three recent events have revived interest in this side reaction to iodide: alarming reports from Germany regarding the dangers to the thyroid gland of radiographic contrast media, the widespread use of the iodine-containing drug amiodarone, and the proposed use of potassium iodide (KI) (100-200 mg/day) as the most effective protective measure against released radioactive iodine isotopes after loss of coolant accidents in nuclear reactors.” This review was written before the drug amiodarone was approved for use in the USA, after causing havoc in Europe. Amiodarone contains organic iodine. The use of inorganic iodine/iodide at 9 mg/day was never tested in similar patients as an alternative to amiodarone, a drug releasing about 9 mg iodine per day. It would not be surprising if 9 mg inorganic iodine/iodide/day resulted in the beneficial effects without the severe side effects. Radiographic contrast media contains organic iodine. Last, the authors mentioned potassium iodide (KI) at daily dose of 100-200 mg, which is the only inorganic form of iodide included in the list of agents causing “iodide-induced thyrotoxicosis”. However, in the same review, the authors stated: “Although there are scattered case reports of IIT (iodide-induced thyrotoxicosis) after the use of KI, these must be considered in the light of over 108 tablets of KI prescribed annually in this country. Reports of experience with KI (1.6-6.4 g/day) in large series of pulmonary patients revealed no hyperthyroidism in 2404 and 502 patients.” Nevertheless when iodine is incorporated into drugs, inorganic iodide is blamed for the side effects. “Hyperthyroidism occurring after administration of iodine-containing drugs has been ascribed to iodide.” (79). The thyrotoxicosis induced by iodine-containing drugs are blamed on inorganic iodide even though the use of inorganic iodide alone was not associated with thyrotoxicosis in the 2 studies referred to. Does that make any sense? Iodophobia, induced by whatever motivation, causes an altered state of consciousness, which makes doublespeak and contradictory statements acceptable.
There is a great need to educate physicians about the great difference between organic iodine and inorganic iodine/iodide. One good example to demonstrate this difference is the thyroid hormones T4 and T3. They are organic iodine-containing substances that occur naturally. Their effects are well described and distinctly different from the effects of inorganic iodine/iodide. No physician has ever attributed the effects of thyroid hormones to inorganic iodine/iodide. So, why is it so hard for them to extrapolate this observation to organic iodine containing drugs?? Here again, the answer may be in two symptoms of medical iodophobia: Altered state of consciousness and split personality, allowing a complete dissociation in their thinking process between the organic iodine-containing thyroid hormones and the organic iodine containing drugs.
VI. Iodization of salt and chronic autoimmune thyroiditis: A proposed pathophysiology
In several communities worldwide, an increased incidence of chronic autoimmune thyroiditis was reported following implementation of iodization of sodium chloride (80). In areas of the United States where this relationship has been studied, mainly in the Great Lakes Region, a similar trend was reported. In 1966 and 1968 Weaver et al (81,82) from Ann Arbor Michigan reported: “The salient histopathological feature of the thyroid glands, removed at operation in a five-year period before iodine prophylaxis (1915 to 1920), was the paucity of lymphocytes in their parenchyma, and, more importantly, the absence of thyroiditis of any form” “It should be emphasized that the thyroid glands prior to the use of iodized salt were devoid of lymphocytes, and nodular colloid goiters with dense lymphocytic infiltrates were found after the introduction of iodized salt in 1924”. It is of interest to note that prior to iodization of salt, autoimmune thyroiditis was almost non-existent in the USA, although Lugol solution and potassium iodide were used extensively in medical practice in amounts 2 orders of magnitude greater than the average daily amount ingested from iodized salt. This suggests that inadequate iodide intake aggravated by goitrogens, not excess iodide, was the cause of this condition. To be discussed later, autoimmune thyroiditis cannot be induced by inorganic iodide in laboratory animals unless combined with goitrogens, therefore inducing iodine deficiency.
Furszyfer et al (83), from the Mayo Clinic, studied the average annual incidence of Hashimoto’s thyroiditis among women of Olmsted County, Minnesota during 3 consecutive periods covering 33 years of observation, from 1935 to 1967. They found the incidence to be higher in women 40 years and older versus women 39 years and less. However, in both groups, there was a progressive increase in the incidence of Hashimoto’s thyroiditis over time. During the 3 periods evaluated, that is 1935-1944; 1945-1954; 1955-1967; the average annual incidence of Hashimoto’s per 100,000 population were 2.1; 17.9; and 54.1 for women 39 years and less. For women 40 years and older, the average annual incidence over the same 3 periods were: 16.4; 27.4; and 94.1. The authors commented: “From this study it appears that there has been an increase in the incidence rate of Hashimoto’s thyroiditis in Olmsted County between 1935 and 1967.” “One of the more attractive hypotheses with respect to the change in the incidence of Hashimoto’s thyroiditis (and perhaps other thyroid disorders) is that increased ingestion of iodide (For the reader’s information, they are talking about iodization of salt) triggers the disease, but obviously, this is not the only factor to be considered in its pathogenesis.”
Doctor Hashimoto’s name became a household word thanks to four thyroid glands. In 1912, pathologist H. Hashimoto published in the German language and in a German medical journal (84), his histological findings in four thyroid glands removed at surgery: numerous lymphoid follicles; extensive connective tissue formation; diffuse round cell infiltration; and significant changes of the acinar epithelium. He called this pathology of the thyroid “struma lymphomatosa”. At the time of this publication, autoimmune thyroiditis was not observed in the U.S. population until the iodization of salt. Hashimoto’s thyroiditis is now classified as goitrous autoimmune thyroiditis because the gland is enlarged, in distinction to atrophic autoimmune thyroiditis where atrophy and fibrosis are predominant. Both conditions are chronic, progressing over time to hypothyroidism in a significant percentage of patients (71,81). It is important to point out that the Mayo Clinic study started 10-15 years after implementation of iodization of salt in the area. Therefore, even during the first decade of observation, the prevalence of autoimmune thyroiditis was already significant. Again, it must be emphasized that prior to the implementation of iodized salt as observed by Weaver et al (81,82), this pathology of the thyroid gland was not reported in the USA, even though the Lugol solution and potassium iodide was used extensively in medical practice at that time in daily amount 2 orders of magnitude greater than the average intake of iodide from table salt.
The mechanism by which iodide induces autoimmune thyroiditis is poorly understood. Experimentally induced autoimmune thyroiditis in laboratory animals by acutely administered iodide required the use of antithyroid drugs, essentially goitrogens, to produce these effects (85-88). These goitrogens induced thyroid hyperplasia and iodide deficiency. Antioxydants either reduced or prevented the acute iodide-induced thyroiditis in chicks (89) and mice (90). Bagchi et al (89) and Many et al (90) proposed that the thyroid injury induced by the combined use of iodide and goitrogens occurs through the generation of reactive oxygen species.
We would like to propose a mechanism for the oxidative damage caused by low levels of iodide combined with antithyroid drugs: Inadequate iodide supply to the thyroid gland, aggravated by goitrogens, activates the thyroid peroxydase (TPO) system through elevated TSH, low levels of iodinated lipids, and high cytosolic free calcium, resulting in excess production of H2O2. The excess H2O2 production is evidenced by the fact that antioxidants used in Bagchi’s experiments did not interfere with the oxidation and organification of iodide and therefore neutralized only the excess oxydant (89). This H2O2 production is above normal due to a deficient feedback system caused by high cytosolic calcium due to magnesium deficiency and low levels of iodinated lipids which requires for their synthesis iodide levels 2 orders of magnitude greater than the RDA for iodine. Once the low iodide supply is depleted, TPO in the presence of H2O2 and organic substrate reverts to its peroxydase function which is the primary function of haloperoxydases, causing oxidative damage to molecules nearest to the site of action: TPO and the substrate thyroglobulin (Tg). Oxydized TPO and Tg elicit an autoimmune reaction with production of antibodies against these altered proteins with subsequent damage to the apical membrane of the thyroid cells, resulting in the lymphocytic infiltration and in the clinical manifestations of Hashimoto’s thyroiditis. In laboratory animals prone to autoimmune thyroiditis, the genetic defect may be in the production of H2O2 in excess of what is needed.
The iodination of thyrosine residues by TPO requires the presence of Tg, H2O2 and iodide. The supply of H2O2 comes from the NADPH oxydase system (91). This system is inhibited by certain iodinated lipids (92-95) and is enhanced by cytosolic free calcium Ca++ (89 and vide infra). The equation for organification of iodide by TPO is displayed in Fig. 1, together with the feedback system controlling the production of H2O2. The logical deduction from this equation is that increased cytosolic free calcium will cause an excess of H2O2. Increased levels of iodinated lipids on the other hand, would limit the production of H2O2. How much iodide is required for the production of iodinated lipids? In 1976, Rabinovitch et al (96) reported their results regarding the effect of 3 levels of iodide supplementation on the production of iodinated lipids in the thyroid glands of dogs: low iodide diet, normal iodide diet, and high iodine diet. The dogs were kept on those diets for 6 weeks. Iodinated lipids in the plasma membrane and in the cell total lipids were observed only in the dogs receiving the high iodide diet. What about human subjects? In 1994, Dugrillon et al (97) reported for the first time the presence of 5-hydroxy-6-iodo- 8,11,14-eicosatrienoic delta lactone (delta iodolactone) in a human thyroid, following the ingestion of 15 mg iodide/day for 10 days in the host. It was the first time this biologically active iodolipid was isolated from human thyroid glands. The amount of iodide the host received was 100 times the RDA, but it is the amount of iodine/iodide we recommended for orthoiodosupplementation (30). Dugrillon et al (97) stated: “These results demonstrate for the first time that delta-iodo-lactone is present in iodide treated human thyroid.”
Magnesium deficiency, which is prevalent in the U.S. population, results in increased levels of cytosolic free calcium (98). Intracellular free calcium levels above the normal range are cytotoxic causing calcification of mitochondria and cell death. The cell membrane possesses an ATP-dependant calcium pump that keeps intracellular levels of free ionized calcium within narrow limits. This calcium pump is magnesium dependant for normal function. Magnesium deficiency results in a defective calcium pump and intracellular accumulation of ionized calcium. Inadequate iodine/iodide intake below orthoiodosupplementation results in decreased levels of delta-iodo-lactone. Combined magnesium and iodine/iodide deficiency based on the concept of orthoiodosupplementation are the basic factors involved in the oxidative damage caused by excess H2O2 and reactive oxygen species. If this proposed mechanism is valid, orthoiodosupplementation (30) combined with magnesium intake between 800-1200 mg/day, a daily amount this author recommended 21 years ago (98) for magnesium sufficiency, should reverse autoimmune thyroiditis. This nutritional approach is also effective in Graves’ autoimmune thyroiditis as previously discussed.
VII. Implementation of orthoiodosupplementation as part of a total nutritional program
The thyroid gland, like the rest of the body needs adequate amounts of all the macro- and micronutrients to function optimally. Ideally, besides orthoiodosupplementation and magnesium in adequate amounts, a complete nutritional program would be most appropriate since other essential nutrients are important for thyroid function and are involved in overall wellbeing. Since thyroid disorders occur predominantly in women (30), it is appropriate to mention the beneficial effects of a magnesium-emphasized nutritional program on the wellbeing of women suffering from premenstrual tension syndrome, post-menopausal osteoporosis and fibromyalgia (99-103). This nutritional program combined with orthoiodosupplementation is the safest of the options available to prevent and to treat thyroid diseases in women.
Radioiodide in the treatment of Graves’ disease induces hypothyroidism in 90% of patients within the first year, with a continuing rate of 2-3% per year thereafter (76). The use of radioiodide in the treatment of Graves’ disease has been associated with leukemia and other forms of cancer (104). Fever and arthralgia are reported in 1-5% of patients on goitrogens (antithyroid drugs) (76). Patients on goitrogens may be more prone to infections due to inadequate supply of iodide to leucocytes during phagocytosis, discussed in the following paragraph. Goitrogens can induce severe hepatotoxicity, requiring liver transplantation and sometimes resulting in death (105).
A totally neglected area is the effect of goitrogens on other haloperoxydases such as myeloperoxydases, involved in the defense mechanism against infections. Myeloperoxydase is present in high concentrations in the granules of polymorphonuclear leucocytes and monocytes (106). It catalyses the oxidation of iodide, bromide and chloride in the presence of H2O2 , to yield products that oxydize and halogenate microbial components (107,108). Chloride, due to its high concentration in leucocytes (109) is believed to be the main halogen used by myeloperoxydase. However, leucocytes have the ability to concentrate iodide 300 fold during phagocytosis (110) and even deiodinate thyroid hormones to generate inorganic iodide when iodide supply is inadequate (111). Incubated in the presence of 10 ug iodide/100 ml of incubation media, phagocytosing leucocytes concentrated inorganic iodide 300 fold to achieve intracellular concentration of 0.003% inorganic iodide. Leucocyte proteins contained even higher concentrations of organic iodine, 0.04%, that is a 4000 fold higher concentration of iodine than present in the incubation media. Thyroxine synthesis was observed during phagocytosis of leucocytes, when the iodide supply was adequate (10 ug/100 ml) (110). However, in the absence of nonradioactive iodide, phagocytosing human leucocytes metabolized thyroid hormones added to the incubation media in order to generate free inorganic iodide (111). Klebanoff and Green (111) commented that iodide, on a molar basis, was much more effective than chloride in the antimicrobial activity of myeloperoxydase of leucocytes and stated: “When the iodide supply is diminished, the concentration of chloride… may be adequate.” These authors observed a significant interference with the antimicrobial activity of myeloperoxydase of leucocytes by antithyroid drugs (goitrogens).
Based on our previous calculations (30), the concentration of iodide used by Stole (110), that is 10 ug/100ml, roughly 10-6 Molar, is equivalent to the expected serum levels of inorganic iodide in patients on orthoiodosupplementation and also in mainland Japanese who consume an average daily amount of 13.8 mg of elemental iodine (30), the only population in the world on orthoiodosupplementation and one of the healthiest based on cancer statistics (30). From data available in published studies regarding the effect of increasing amounts of iodide on serum inorganic iodide levels at steady state conditions (112,113), we have calculated the expected serum levels of inorganic iodide at steady state conditions, when a patient is on orthoiodosupplementation (Fig. 2).
It is of interest to note that a daily ingestion of 12.5 mg iodine/iodide resulted in serum inorganic iodide level of 2 x 10-6 M, which is the serum level reported by Wolff-Chaikoff (27), to cause inhibition of organic binding of iodine and therefore inhibition of synthesis of thyroid hormones. Since this amount of Lugol solution was used safely by three generations of physicians for iodine supplementation, and since we have observed that patients reported optimal mental and physical performances on 3 to 4 times that amount, we would like to propose a redefinition of the Wolff-Chaikoff Effect as a beneficial effect on mental and physical performances.
The breakdown of thyroid hormones by phagocytosing leucocytes in an iodine-deficient patient could explain the high incidence of hypothyroxinemia in patients with chronic infections such as chronic active hepatitis (114). Accelerated thyroid hormone degradation during bacterial infection has been reported in man (115) and rhesus monkeys (116,117). Such findings would not be expected in mainland Japanese and in patients on orthoiodosupplementation because the calculated serum levels of iodide in those subjects would approximate the concentration of iodide in Stole’s incubation media (26,110). Wartofsky and Burman (114) in their review article on the “Euthyroid Sick Syndrome” wrote: “This review will address the effects of nonthyroidal illness on thyroid function and attempt to establish guidelines for the determination as to whether such patients are truly euthyroid or not. Indeed the ultimate question for the clinician often is whether to treat the individual with severe nonthyroidal illness for low serum thyroxine (T4):” Although the recommended treatment in such cases would obviously be the administration of thyroid hormones, it would be more physiological to implement orthoiodosupplementation in these patients since the thyroid hormones administered to the iodine-deficient patient will be deiodinated to generate free iodide. So why not give them inorganic nonradioactive iodine/iodide in the form of orthoiodosupplementation? Thyroid hormones are very expensive forms of the element iodine, which is what these patients really need to start with.
The concept of orthoiodosupplementation (30) is based on the self-evident fact that the whole body, not just the thyroid gland, needs iodine. The whole body needs this essential trace element which plays different roles in different organs and tissues. In order to assess whole body sufficiency for iodine/iodide, a simple loading test was developed (118), based on the concept that the more deficient a patient is in this nutrient, the greater the percentage of ingested iodine/iodide that will be retained, the smaller the percentage excreted in the urine.
During the late 1800’s and early 1900’s, orthoiodosupplementation was administered with Lugol solution 0.1-0.3 ml containing 12.5-37.5 mg of iodine/iodide (46). Because administration of Lugol solution is not very accurate, may stain clothing, has an unpleasant taste and causes gastric irritation, we decided to use a precisely quantified tablet form (Iodoral®) containing 5 mg iodine and 7.5 mg iodide as the potassium salt (119). To prevent gastric irritation, the iodine/iodide preparation was absorbed unto a colloidal silica excipient; and to eliminate the unpleasant taste of iodine, the tablets were coasted with a thin film of pharmaceutical glaze. Ten clinically euthyroid Caucasian women were evaluated before and 3 months after ingesting a tablet daily. The evaluation included thyroid function tests and assessments of thyroid volume by ultrasonometry. The results suggest that this form and amount administered daily for 3 months to euthyroid women had no detrimental effect on thyroid volume and functions.
When tested in the loading test, one tablet was not sufficient to distinguish between different degrees of iodine deficiency because the interindividual variation was very small. We were interested in a loading test that would result in 40-50% of the ingested dose excreted in the 24hr urine and also with a wide range of values in different subjects. For 6 subjects tested, the following percent dose excreted were obtained, expressed as mean ± SD (range): one tablet = 22 ± 1.2 (20-26); two tablets = 23 ± 2.8 (22-25); three tablets = 25 ± 12.3 (26-37). Another group of 6 normal subjects on a similar Western diet was tested with four tablets and the values were = 39 ± 17.2 (14.2 – 66). (See Fig. 3)
We chose 4 tablets for the loading test. Sufficiency of the whole human body for iodine/iodide was arbitrarily defined as 90% or more of the ingested amount excreted in the 24hr urine collection, using 50 mg of the iodine/iodide preparation (4 tablets). Orthoiodosupplementation with one tablet a day required up to 18 months to achieve sufficiency in some patients, and in others, sufficiency was not achieved even after 2 years of supplementation with one tablet/day. With 3-4 tablets/day, however, sufficiency was achieved within 3 months in most cases. These data support the keen observations of clinicians over the past century, regarding the amount of iodine/iodide needed for iodine/iodide supplementation, between 12.5 mg and 37.5 mg elemental iodine from Lugol solution.
Orthoiodosupplementation increased urinary excretion of lead, cadmium, arsenic, aluminum and mercury. Urinary bromide and fluoride levels increased markedly and proportionally to the amount of iodine/iodide ingested. At 3 tablets a day, urinary fluoride and bromide increased up to 20 fold, although the pre-loading test levels were not elevated (120). Obesity seems to increase the requirement for iodine/iodide, and this may be due to sequestration of iodine by unsaturated fats. So many factors affect the requirement of iodine/iodide that the best way to assess whole body sufficiency for this element is with the loading test.
Orthoiodosupplementation decreased the need for thyroid hormones in patients on these hormones. In some cases, this occurred during the first months of orthoiodosupplementation (30). However, in a patient with atrophic autoimmune thyroiditis, 11 months of orthoiodosupplementation was required before decreasing the amount of thyroid hormones. A 54 year old female patient with atrophic autoimmune thyroiditis (thyroid volume by ultrasound = 2.8 ml) and elevated TPO Ab titers, on 150 ug of T4 was placed on orthoiodosupplementation with 3-4 tablets/day. The presupplementation loading test revealed 23% iodide excreted. After 3 months on orthoiodosupplementation, her loading test was 92% of iodide excreted. Her serum T4 levels progressively increased to reach above normal level (14.6 ug %; normal range 4.5–12) after 11 months on orthoiodosupplementation. T4 supplementation was decreased from 150 ug to 100 ug/day. She stated that since on orthoiodosupplementation, she feels more energetic with a clearer mind, and with an improved sense of wellbeing.
If indeed, iodine deficiency, that is iodine/iodide intake below orthoiodosupplementation levels, is involved in autoimmune thyroiditis, then diseases that are associated with autoimmune thyroiditis may also be caused by iodine deficiency. Giani et al (121) in 1996 reported a significant association of breast cancer with Hashimoto’s thyroiditis. When 100 consecutive patients with breast cancer were compared with 100 match controls, Hashimoto’s thyroiditis was present in 2% of the control group compared with 13.7% in the group with breast cancer. Simple goiter, a sign of iodine deficiency, was present in 11% of controls compared to 27.4% of the patients with breast cancer. Diabetes may also be an iodine-deficiency disease. Lindberg et al (122) compared 52 diabetic children (insulin-dependant) with 386 non-diabetic school children. TPO antibodies were present in 6% of the control group, compared with 38% of diabetic children. It seems like thyroidologists and nutritionists dropped the ball and missed the boat. Such a simple, safe, inexpensive way to heal so many medical conditions!! An overview of the effects of orthoiodosupplementation on mental performance, resistance to infections, protection of the thyroid gland against radioactive fallout, detoxification of heavy metals and of the toxic halides bromide and fluoride, suggests that orthoiodosupplementation may be the best and safest preventive measure against bioterrorism. The corollary then would be: The worse form of domestic bioterrorism is the dissemination of iodophobic misinformation in order to discourage the use of orthoiodosupplementation.
1) Bernecker, C., Intermittent therapy with potassium iodide in chronic obstructive disease of the airways. Acta Allerg., 24:216, 1969.
2) National Council on Radiation Protection and Measurements: Protection of the thyroid gland in the event of release of radioiodine. NCRP Report No. 55, NCRP, Washington, D.C. 1977.
3) Hercheimer, H., Effect of iodide treatment on thyroid function. N. Engl. J. Med., 297:171, 1977.
4) Phillippou, G., Koutras, D.A., Piperingos, G., et al, The effect of iodide on serum thyroid hormone levels in normal persons, in hyperthyroid patients, and in hypothyroid patients on thyroxine replacement. Clin. Endocr., 36:573-578, 1992.
5) Anonymous. Sur un nouvel acide forme avec la substance decouverte par M. Courtois. Annales de Chimie, 88:311-318, 1813.
6) Bertrand, G., Sur l’emploi favorable du manganese comme engrais. In Comptes rendus de l’Academie des sciences, 141:1255-1257, 1905.
7) Marine, D., Kimball, O.P., Prevention of Simple Goiter in Man. Arch. Intern. Med., 25:661, 1920.
8) Marine, D., Prevention and Treatment of Simple Goiter. Atl. Med. J., 26:437-442, 1923.
9) Delange, F.M., Iodine Deficiency. In Werner & Ingbar’s The Thyroid – Braverman LE and Utiger RD Editors, Lippincott Williams & Wilkins, 295-329, 2000.
10) Kendall, E.C., The isolation in crystalline form of the compound which occurs in the thyroid: its chemical nature and physiologic activity. JAMA, 64:2042-2043, 1915.
11) Harington, C.R., Isolation of Thyroxine from the Thyroid Gland. Biochem. Jour., 20:293-299, 1926.
12) Gross, J., Pitt-Rivers, R., Physiological activity of 3:5:3’ –L-triiodothyronine. Lancet 1:593, 1952.
13) Roche, J., Lissitsky, S., Michel, R., Sur la presence de triiodothyronine dans la thyroglobuline. Compt. Rend. Acad. Sci., 234:1228, 1952.
14) Kelly, Francis C., Iodine in Medicine and Pharmacy Since its Discovery – 1811-1961. Proc R Soc Med 54:831-836, 1961.
15) Braverman, Lewis E., Iodine and the Thyroid: 33 Years of Study. Thyroid, 4:351-352, 1994.
16) Hitchens, A.P., The Emergency Treatment of Water for Drinking Purposes. Milit. Sug., 51:657-662, 1922.
17) Freund, A.P., Thomas, W.C., Bird, E.D., et al, Effect of Iodinated Water Supplies on Thyroid Function. J. Clin. Endocr., 26:619-624, 1966.
18) Byrd, O.E., Malkin, H.M., Reed, G.B., et al, Safety of Iodine as a Disinfectant in Swimming Pools. Public Health Reports, 78:393-397, 1963.
19) Thomas, W.C., Black, A.P., Freund, G., et al, Iodine Disinfection of Water. Arch. Environ. Health, 19:124-128, 1969.
20) LeMar, H.J., Georgitis, W.J., McDermott, M.T., Thyroid Adaptation to Chronic Tetraglycine Hydroperiodide Water Purification Tablet Use. J. Clin. Endocr. & Metab., 80:220-223, 1995.
21) McMonigal, K.A., Braverman, L.E., Dunn, J.T., et al, Thyroid Function Changes Related to Use of Iodinated Water in the U.S. Space Program. Aviation, Space, and Environ. Med., 71:1120-1125, 2000.
22) Pearce, E.N., Gerber, A.R., Gootnick, D.B., et al, Effects of Chronic Iodine Excess in a Cohort of Long-Term American Workers in West Africa. J. Clin. Endocr. & Metab., 87:5499-5502, 2002.
23) Pittman et al, Thyroidal Radioiodine Uptake. N. Engl. J. Med., 280:1431-1434, 1969.
24) Wartofsky, L., Ingbar, S.H., Estimation of the Rate of Release of Non-thyroxine Iodine from the Thyroid Glands of Normal Subjects and Patients with Thyrotoxicosis. J. Clin. Endocr., 33:488-500, 1971.
25) London, W.T., Vought, R.L., Brown, F.A., Bread – a Dietary Source of Large Quantities of Iodine. New Engl. J. Med., 273:381, 1965.
26) Stanley, M.M., The direct estimation of the rate of thyroid hormone formation in man. The effect of the iodide ion on thyroid iodine utilization. J. Clin. Endocr., 9:941-954, 1949.
27) Wolff, B.J., Chaikoff, I.L., Plasma Inorganic Iodide as a Homeostatic Regulator of Thyroid Function. J. Biol. Chem., 174:555-564, 1948.
28) Wolff, J., Iodide Goiter and the Pharmacologic Effects of Excess Iodide. Am. J. Med., 47:101-124, 1969.
29) Wartofsky, L., Ransil, B.J., Ingbar, S.H., Inhibition by Iodine of the Release of Thyroxine from the Thyroid Glands of Patients with Thyrotoxicosis. J. Clin. Invest., 49:78-86, 1970.
30) Abraham, G.E., Flechas, J.D., Hakala, J.C., Orthoiodosupplementation: Iodine sufficiency of the whole human body. The Original Internist, 9:30-41, 2002.
31) Pennington, J.A., Schoen, S.A., Total Diet Study: Estimated Dietary Intakes of Nutritional Elements, 1982-1991. Internat. J. Vit. Nutr., 66:350-362, 1996.
32) Vobecky, M., Babicky, A., Effect of Enhanced Bromide Intake on the Concentration Ratio I/Br in the Rat Thyroid Gland. Bio. Trace Element Research, 43:509-513, 1994.
33) Velicky, J., Titlbach, M., Duskova, J., et al, Potassium bromide and the thyroid gland of the rat: morphology and immunohistochemistry, RIA and INNA analysis. Ann. Anat., 179:421-431, 1997.
34) Van Leeuwen, F.X.R., Hanemaauer, R., Loeber, J.G., The Effect of Sodium Bromide on Thyroid Function. Arch. Toxicol. Suppl., 12:93-97, 1988.
35) Abraham, G.E., Iodine Supplementation Markedly Increases Urinary Excretion of Fluoride and Bromide. Townsend Letter, 238:108-109, 2003.
36) Shimomura, K., Mullinix, M.G., Kakunaga, T., et al, Bromine residue at hydrophilic region influences biological activity of aplysiatoxin, a tumor promoter. Science, 222:1242-1244, 1983.
37) Sangster, B., Blom, J.L., Sekhuis, V.M., et al, The Influence of Sodium Bromide in Man: A Study in Human Volunteers with Special Emphasis on the Endocrine and the Central Nervous System. Fd. Chem. Toxic., 21:409-419, 1983.
38) Torii, S., Mitsumori, K., Inubushi, S., et al, The REM Sleep-Inducing Action of a Naturally Occurring Organic Bromine Compound in the Encephalc Isole Cat. Psychopharmacologia (Berl.), 29:65-75, 1973.
39) Dictionary of Scientific Biography. Gillispie, C.C. Editor, Simon & Schuster, New York, 1970.
40) Coindet, J.F., Decouverte d’un nouveau remede contre le goitre. Ann. Clin. Phys., 15:49, 1820.
41) Coindet, J.F., Nouvelles recherches sur les effets de l’iode, et sur les precautions a suivre dans le traitement de goitre par le nouveau remede. Bibl. Univ. Sci. Belle-Lettres Arts. 16:140, 1821.
42) Lugol, J.G.A., Memoire sur l’emploi de l’iode dans les maladies scrophuleuses. Paris, 1829. (Published by himself).
43) Boussingault, J.B., Recherches sur la cause qui produit le goitre dans les Cordilieres de la Nouvelle-Grenade. Ann. Chim. Phys., 48:41, 1831.
44) Hartsock, C.L., Iodized Salt in the Prevention of Goiter. Jour. Amer. Med. Assoc., 86:1334-1338, 1926.
45) Thompson, W.O., Brailey, A.G., Thompson, P.K., et al, The Range of Effective Iodine Dosage in Exophthalmic Goiter III. Arch. Int. Med., 45:430, 1930.
46) Gennaro A.R., Remington: The Science and Practice of Pharmacy, 19th Edition, 1995, Mack Publishing Co., 1267.
47) Cohn, B.N.E., Absorption of Compound Solution of Iodine from the Gastro-Intestinal Tract. Arch. Intern Med., 49:950-956, 1932.
48) Diagnosis and Treatment of Diseases of the Thyroid Gland. Editor Amy F. Rowland, W.B. Saunders Company, 1932, pg. 98.
49) Beebe, S.P., Iodine in the Treatment of Goiter. M. Rec., 99:996-999, 1921.
50) Brent, G.A., Larsen, P.R., Treatment of Hypothyroidism. In Werner & Ingbar’s The Thyroid – Braverman LE and Utiger RD Editors, Lippincott Williams & Wilkins, 853-858, 2000.
51) Ghandrakant, C., Kapdim MD, Wolfe, J.N., Breast Cancer. Relationship to Thyroid Supplements for Hypothyroidism. JAMA, 238:1124, 1976.
52) Braverman, L.E., Utiger, R.D., Introduction to Thyrotoxicosis. In Werner & Ingbar’s The Thyroid – Braverman LE and Utiger RD Editors, Lippincott Williams & Wilkins, 515-517, 2000.
53) Von Basedow, G.A., Exophthalmos durch Hyperrophie des Zellgewebca in der Augenhoehle. Wsrchr. Ges. Heilk, 6:197, 1840.
54) Stokes, W., Diseases of the Heart and Aorta. Hodges and Smith, Dublin, p.278, 1854.
55) Trousseau, A., Lectures on Clinical Medicine. vol. 1, lecture XIX, Exophthalmic goitre of Graves’ disease, New Sydenham Society, London, p.586, 1868.
56) Trousseau, A., Lectures on Clinical Medicine. vol. 1, lecture XIX, Exophthalmic goitre of Graves’ disease, New Sydenham Society, London, p.587, 1868.
57) Thompson, W.O., Thompson, P.K., Brailey, A.G., et al, Prolonged Treatment of Exophthalmic Goiter by Iodine Alone. Arch. Int. Med., 45:481-502, 1930.
58) Kocher, T., Discussion on the Surgical Treatment of Graves’s Disease. Brit. Med. Jour., ii:931-939, 1910.
59) Kocher, T., Ueber Jodbasedow. Arch. L. Klin. Chir., 92:1166, 1910.
60) Cowell, S.J., Mellanby, E., The Effect of Iodine on Hyperthyroidism in Man. Quart. J. Med., 18:1-18, 1924-1925.
61) DeCourcy, J.L., The Use of Lugol’s Solution in Exophthalmic Goitre. Ann. Surg., 86:871-876, 1927
62) Plummer, H.S., Boothby, W.M., The Value of Iodine in Exophthalmic Goiter. J. Iowa Med. Soc., 14:65, 1924.
63) Plummer, W.A., Iodin in the Treatment of Goiter. Med. Cl. North America, 8:1145-1151, 1925.
64) Lahey, F.H., The Use of Iodine in Goitre. Boston Med. & Surg. J., 193:487-490, 1925.
65) Starr, P., Walcott, H.P., Segall, H.N., et al, The Effect of Iodin in Exophthalmic Goiter. Arch, Int. Med., 34:355-364, 1924.
66) Fraser, F.R., Iodine in Exophthalmic Goitre. Brit. Med. J., 1:1, 1925.
67) Astwood, E.B., Treatment of hyperthyroidism with thiourea and thiouracil. JAMA, 122:78-81, 1943.
68) Astwood, E.B., VanderLaan, W.P., Thiouracil Derivatives of Greater Activity for the Treatment of Hyperthyroidism. J. Clin. Endocr., 5:424-430, 1945.
69) Godley, A.F., Stanbury, J.B., Preliminary Experience in the Treatment of Hyperthyroidism with Potassium Perchlorate. J. Clin Endocr. & Metab., 14:70-78, 1954.
70) Wolff, J., Perchlorate and the Thyroid Gland. Pharmacological Reviews, 50:89-105, 1998.
71) Solomon, D.H., Beck, J.C., VanderLaan, W.P. and Astwood, E.B., Prognosis of Hyperthyroidism Treated by Antithyroid Drugs. JAMA, 152:201-205, 1953.
72) Hershman, J.M., Givens, J.R., Cassidy, C.E. and Astwood, E.B., Long-Term Outcome of Hyperthyroidism Treated with Antithyroid Drugs. J. Clin. Endocr. Metab., 26:803-807, 1966.
73) Wartofsky, L., Low Remission After Therapy for Graves Disease. JAMA, 226:1083-1088, 1973.
74) Reynolds, L.R., Kotchen, T.A., Antithyroid Drugs and Radioactive Iodine. Arch. Int. Med., 139:651-653, 1979.
75) Solomon, B., Glinoer, D., Lagasse, R., et al, Current Trends in the Management of Graves’ Disease. J. Clin. Endocr. Metab., 70:1518-1524, 1990.
76) Cooper, D.S., Treatment of Thyrotoxicosis. In Werner & Ingbar’s The Thyroid – Braverman LE and Utiger RD Editors, Lippincott Williams & Wilkins, 691-715, 2000.
77) Markou, K., Georgopoulos, N., Kyriazopoulou, V., et al, Iodine-Induced Hypothyroidism. Thyroid, 11:501-510, 2001.
78) Leger, A.F., Massin, J.P., Laurent, M.F., et al, Iodine-induced thyrotoxicosis: analysis of eighty-five consecutive cases. Euro. J. of Clin. Invest., 14:449-455, 1984.
79) Fradkin, J.E., Wolff, J., Iodide-Induced Thyrotoxicosis. Medicine, 62:1-20, 1983.
80) Gaitan, E., Nelson, N.C., Poole, G.V., Endemic Goiter and Endemic Thyroid Disorders. World J. Surg., 15:205-215, 1991.
81) Weaver, D.K., Batsakis, J.G., Nishiyama, R.H., Relationship of Iodine to “Lymphocytic Goiters”. Arch. Surg., 98:183-186, 1968.
82) Weaver, D.K., Nishiyama, R.H., Burton, W.D., et al, Surgical Thyroid Disease. Arch. Surg., 92:796-801, 1966.
83) Furszyfer, J., Kurland, L.T., Woolner, L.B., et al, Hashimoto’s Thyroiditis in Olmsted County, Minnesota, 1935 through 1967. Mayo Clin. Proc., 45:586-596, 1970.
84) Hashimoto, H., Zur Kenntniss der lymphomatosen Veranderung der Schilddruse (Struma lymphomatosa). Arch. Klin. Chir., 97:219-248, 1912.
85) Weetman, A.P., Chronic Autoimmune Thyroiditis. In Werner & Ingbar’s The Thyroid – Braverman LE and Utiger RD Editors, Lippincott Williams & Wilkins, 721-732, 2000.
86) Follis, R.H., Further observations on thyroiditis and colloid accumulation in hyperplastic thyroid glands of hamsters receiving excess iodine. Lab Invest., 13:1590-1599, 1964.
87) Belshaw, B.E., Becker, D.V., Necrosis of follicular cells and discharge of thyroidal iodine induced by administering iodine to iodine-deficient dogs. J. Clin. Endocr. Metab., 13:466-474, 1973.
88) Mahmoud, I., Colin, I., Many, M.C., et al, Direct toxic effect of iodine in excess on iodine-deficient thyroid gland: epithelial necrosis and inflammation associated with lipofuscin accumulation. Exp. Mol. Pathol., 44:259-271, 1986.
89) Bagchi, N., Brown, T.R., Sundick, R.S., Thyroid Cell Injury Is an Initial Event in the Induction of Autoimmune Thyroiditis by Iodine in Obese Strain Chickens. Endocrinology, 136:5054-5060, 1995.
90) Many, M.C., Papadopoulaous, J., Martic, C., et al, Iodine induced cell damage in mouse hyperplastic thyroid is associated to lipid peroxidation. In: Gordon A, Gross J, Hennenian G (eds) Progress in Thyroid Research. Proceedings of the 10th International Thyroid Conference. Balkema, Rotterdam, 635-638, 1991.
91) Ohayon, R., Boeynaems, J.M., Braekman, J.C., et al, Inhibition of thyroid NADPH-oxidase by 2-iodohexadecanal in a cell-free system. Molecular and Cellular Endocr, 99:133-141, 1994.
92) Krawiec, L., Chazenbalk, G.D., Puntarulo, S.A., et al, The Inhibition of PB125I Formation of Calf Thyroid Caused by 14-Iodo1-5-Hydroxy-Eicosatrienoic Acid is Due to Decreased H2O2 Availability. Horm. Metabol. Res., 20:86-90, 1988.
93) Pisarev, M.A., Chazenbalk, G.D., Valsecchi, R.M., et al, Thyroid autoregulation. Inhibition of goiter growth and of cyclic AMP formation in rat thyroid by iodinated derivatives of arachidonic acid. J. Endocr. Invest., 11:669-674, 1988.
94) Krawiec, L., Chester, H.A., Bocanera, L.V., et al, Thyroid Autoregulation: Evidence for an Action of Iodoarachidonates and Iodide at the Cell Membrane Level. Horm. Metab. Res. 23:321-325, 1991.
95) Pisarev, M.A., Bocanera, L.V., Chestor, H.A., et al, Effect of Iodoarachidonates on Thyroid FRTL-5 Cells Growth. Horm. Metabol. Res., 24:558-561, 1992.
96) Rabinovitz, J.L., Zanger, M., Podoliski, V., Identification by Nuclear Magnetic Resonance of Iodinated Lipids in the Dog Thyroid. Biochem. and Biophys. Res. Com. 68:1161-1168, 1976.
97) Dugrillon, A., Uedelhoven, W.M., Pisarev, M.A., et al, Identification of 6-Iodolactone in Iodide Treated Human Goiter and its Inhibitory Effect on Proliferation of Human Thyroid Follicles. Horm. Metab. Res., 26:465-469, 1994.
98) Abraham, G.E., The Calcium Controversy. J. of Appl. Nutr., 34:69-73, 1982.
99) Abraham, G.E., Nutritional Factors in the Etiology of the Premenstrual Tension Syndromes. J. Rep. Med., 28:446-464, 1983.
100) Abraham, G.E., Rumley, R.E., The Role of Nutrition in Managing the Premenstrual Tension Syndromes. J. Rep. Med., 32:405-422, 1987.
101) Abraham, G.E., Grewal, H., A Total Dietary Program Emphasizing Magnesium Instead of Calcium: Effect on the Mineral Density of Calcaneous Bone in Postmenopausal Women on Hormonal Therapy. J. Rep. Med., 35:503-507, 1990.
102) Abraham, G.E., The Importance of Magnesium in the Management of Primary Postmenopausal Osteoporosis. J. Nut. Med., 2:165-178, 1991.
103) Abraham, G.E., Flechas, J.D., Management of Fibromyalgia: Rationale for the Use of Magnesium and Malic Acid. J. Nutr. Med., 3:49-59, 1992.
104) Wartofsky, L., Has the Use of Antithyroid Drugs for Graves’ Disease Become Obsolete? Thyroid, 3:335-344, 1993.
105) Williams, K.V., Nayak, S., Becker, D., et al, Fifty Years of Experience with Propylthiouracil-Associated Hepatotoxicity: What Have We Learned? J. Clin. Endocr. Metab., 82:1727-1733, 1997.
106) Schultz, J., Kaminker, K., Myeloperoxidase of the Leucocyte of Normal Human Blood. Arch. Biochem. & Biophys., 96:465-467, 1962.
107) Morrison, M., Schonbaum, G.R., Peroxidase-Catalyzed Halogenation. Ann. Rev. Biochem., 45:861-888, 1976.
108) Thomas, J.A., Hager, L.P., Molecular Iodine as an Obligate Intermediate in the Iodination of Tyrosine by Chloroperoxidase. Biochem. & Biophyscial Research Comm., 35:444-450, 1969.
109) Baron, D.N., Ahmed, S.A., Intracellular Concentrations of Water and of the Principal Electrolytes Determined by Analysis of Isolated Human Leucocytes. Clin. Sci., 37:205-219, 1969.
110) Stole, V., Stimulation of Iodoproteins and Thyroxine Formation in Human Leukocytes by Phagocytosis. Biochem. Biophys. Res. Commun., 45:159-168, 1971.
111) Klebanoff, S.J., Green. W.L., Degradation of Thyroid Hormones by Phagocytosing Human Leukocytes. J. Clin. Invest., 52:60-72, 1973.
112) Fisher, D.A., Oddie, T.H., Epperson, D., Effect of Increased Dietary Iodide on Thyroid Accumulation and Secretion in Euthyroid Arkansas Subjects. J. Clin. Endocr., 25:1580-1590, 1965.
113) Koutras, D.A., Alexander, W.D., Harden, R.M., et al, Effect of Small Iodine Supplements on Thyroid Function in Normal Individuals. J. Clin. Endocr., 24:857-862, 1964.
114) Wartofsky, L., Burman, K.D., Alterations in Thyroid Function in Patients with Systemic Illness: The “Euthyroid Sick Syndrome”. Endocrine Reviews, 3:164-217, 1982.
115) Gregerman, R.I., Solomon, N., Acceleration of thyroxine and triiodothyronine turnover during bacterial pulmonary infections and fever: implications for the functional state of the thyroid during stress and senescence. J. Clin. Endocr. Metab., 27:93, 1967.
116) Woeber, K.A., Alterations in thyroid hormone economy during acute infection with Diplococcus pneumoniae in the rhesus monkey. J. Clin. Invest. 50:378, 1971.
117) DeRubertis, F.R., Woeber, K.A., Evidence for enhanced cellular uptake and binding of thyroxine in vivo during acute infection with Diplococcus pneumoniae. J. Clin. Invest. 51:788, 1972.
118) Abraham, G.E., et al, Measurement of urinary iodide levels by ion-selective electrode: Improved sensitivity and specificity by chromatography on anion-exchange resin. Optimox Research Info #IOD-03. (Reprint available upon request).
119) Abraham, G.E., Flechas, J.D., Hakala, J.C., Optimum Levels of Iodine for Greatest Mental and Physical Health. The Original Internist, 9:5-20, 2002.
120) Abraham, G.E., Iodine Supplementation Markedly Increases Urinary Excretion of Fluoride and Bromide. Townsend Letter, 238:108-109, 2003.
121) Giani, C., Fierabracci, P., Bonacci, R., et al, Relationship between Breast Cancer and Thyroid Disease: Relevance of Autoimmune Thyroid Disorders in Breast Malignancy. J. Clin. Endocr. Metab., 81:990-994, 1996.
122) Lindberg, B., Ericsson, U-B, Ljung, R., et al, High prevalence of thyroid autoantibodies at diagnosis of insulin-dependent diabetes mellitus in Swedish children. J. Lab. Clin. Med., 130:585-589, 1997.