Bromines All Around You
Bromines are common endocrine disruptors, and are part of the halide family, a group of elements that includes fluorine, chlorine and iodine. What makes it so dangerous is that it competes for the same receptors that are used to capture iodine.
If you are exposed to a lot of bromine, your body will not hold on to the iodine that it needs. And iodine affects every tissue in your body -- not just your thyroid.
You are already exposed to far too much chlorine and bromine. Bromine can be found in a number of places in your everyday world, including:
•Pesticides (specifically methyl bromide, used mainly on strawberries, predominantly in California)
•Plastics, like those used to make computers
•Bakery goods and some flours often contain a "dough conditioner" called potassium bromate
•Soft drinks (including Mountain Dew, Gatorade, Sun Drop, Squirt, Fresca and other citrus-flavored sodas), in the form of brominated vegetable oils (BVOs)
•Medications such as Atrovent Inhaler, Atrovent Nasal Spray, Pro-Banthine (for ulcers), and anesthesia agents
•Fire retardants (common one is polybromo diphenyl ethers or PBDEs) used in fabrics, carpets, upholstery, and mattresses
•Bromine-based hot tub and swimming pool treatments
According to van Leeuwen, who has extensively studied the effects of sodium bromide on thyroid function:
"Although the bromide ion is widely distributed in nature, the main route of exposure in humans stems from bromide residues in food commodities as a result of the abundant use of bromide-containing pesticides, like methylbromide and ethylene dibromide, for soil fumigation in intensive horticulture and for postharvest treatment."
One clinical consequence of overexposure to bromine is suppression of your thyroid, leading to hypothyroidism, which will be discussed shortly. Another is bromide toxicity.
Bromine -- The Bully of the Halide Group
When you ingest or absorb bromine, it displaces iodine, and this iodine deficiency leads to an increased risk for cancer of the breast, thyroid gland, ovary and prostate -- cancers that we see at alarmingly high rates today. This phenomenon is significant enough to have been given its own name -- the Bromide Dominance Theory.
Aside from its effects on your endocrine glands, bromine is toxic in and of itself. Bromide builds up in your central nervous system and results in many problems. It is a central nervous system depressant and can trigger a number of psychological symptoms such as acute paranoia and other psychotic symptoms.
In fact, in an audio interview, physician Jorge Flechas reported that, between 1920 and 1960, at least 20 percent of all hospital admissions for "acute paranoid schizophrenia" were a result of ingesting bromine-containing products.
In addition to psychiatric problems, bromine toxicity can manifest as the following:
•Skin rashes and severe acne
•Loss of appetite and abdominal pain
Baby Boomers might recall a popular product from the 1950s called Bromo-Seltzer. These effervescent granules, developed by the Emerson Drug Company of Baltimore, were used to treat heartburn, upset stomach, indigestion, headaches and hangovers.
Bromo-Selzer's original formula contained 3.2 mEq/teaspoon of sodium bromide -- hence the name. The sedative effect probably explained its popularity as a hangover remedy. Bromides were withdrawn from the American market in 1975 due to their toxicity.
Bromo-Selzer is still on the market, but no longer contains bromide.
Bromines in Your Bread Box: Potassium Bromate
The ban on bromines have not prevented them from sneaking into your foods and personal care products.
You probably are not aware of this, but nearly every time you eat bread in a restaurant or consume a hamburger or hotdog bun you are consuming bromide, as it is commonly used in flours.
The use of potassium bromate as an additive to commercial breads and baked goods has been a huge contributor to bromide overload in Western cultures.
Bromated flour is "enriched" with potassium bromate. Commercial baking companies claim it makes the dough more elastic and better able to stand up to bread hooks. However, Pepperidge Farm and other successful companies manage to use only unbromated flour without any of these so-called "structural problems."
Potassium bromate is also found in some toothpastes and mouthwashes, where it's added as an antiseptic and astringent. It has been found to causebleeding and inflammation of gums in people using these products.
Sodium Bromate and BMOs
Mountain Dew, one of the worst beverages you can drink, uses brominated vegetable oil as an emulsifier. Not only that, it contains high fructose corn syrup, sodium benzoate, more than 55 mg of caffeine per 12 ounce can, and Yellow Dye #5 (tartrazine, which has been banned in Norway, Austria and Germany.)
A weapon of mass destruction -- in a can.
Even drinking water can be a source of bromide. When drinking water containing bromide is exposed to ozone, bromate ions are formed, which are powerful oxidizing agents. Such was the case in 2004 when Coca Cola Company had to recall Dasani bottled water.
Sodium bromate can also be found in personal care products such as permanent waves, hair dyes, and textile dyes. Benzalkonium is used as a preservative in some cosmetics.
Finally, bromine and chlorine were the most common toxic elements reportedly found in automobiles, according to the blog of David Brownstein, MD (March 2007). They showed up in the seats, armrests, door trim, shift knobs and other areas of the car.
Think about how much time you spend enclosed in your outgassing Chevy... windows up with no air circulation.
The United States is quite behind in putting an end to the egregious practice of allowing bromine chemicals in your foods. In 1990, the United Kingdom banned bromate in bread. In 1994, Canada did the same. Brazil recently outlawed bromide in flour products.
What's taking us so long? Another case of our government protecting big industry -- instead of protecting you.
Iodine Levels and Cancer Risk
Iodine levels have significantly dropped due to bromine exposure; declining consumption of iodized salt, eggs, fish, and sea vegetables; and soil depletion. In the U.S. population, there was a 50 percent reduction in urinary iodine excretion between 1970 and 1990.
What's this doing to our country's health?
The Japanese consume 89 times more iodine than Americans due to their daily consumption of sea vegetables, and they have reduced rates of many chronic diseases, including the lowest rates of cancer in the world. The RDA for iodine in the U.S. is a meager 150 mcg/day, which pales in comparison with the average daily intake of 13800 mcg/day for the Japanese.
There is a large body of evidence suggesting that low cancer rates in Japan are a result of their substantially higher iodine levels. Iodine has documented antioxidant and anti-proliferative properties.
A strong case can be made that your iodine RDA should be closer to what the Japanese consume daily, if breast cancer rates are any indication. Low iodine can lead to fibrocystic breast disease in women (density, lumps and bumps), hyperplasia, and atypical mammary tissue. Such fibrocystic changes in breast tissue have been shown to reverse in the presence of iodine supplementation after 3-4 months.
If you are interested in being tested for iodine deficiency, the urine iodine challenge test is the best way to assess your iodine level.
Bromine and Your Thyroid
Adding to the negative health effects of bromine, the damage to your thyroid health deserves special mention.
As stated in the first part of this article, bromine exposure depletes your body's iodine by competing with iodine receptors. Iodine is crucial for thyroid function. Without iodine, your thyroid gland would be completely unable to produce thyroid hormone.
Even the names of the different forms of thyroid hormone reflect the number of iodine molecules attached -- T4 has four attached iodine molecules, and T3 (the biologically active form of the hormone) has three--showing what an important part iodine plays in thyroid biochemistry.
Hypothyroidism is far more prevalent than once thought in the U.S. The latest estimates are that 13 million Americans have hypothyroidism, but the actual numbers are probably higher. Some experts claim that 10 to40 percent of Americans have suboptimal thyroid function.
Many of these folks may actually have nothing wrong with their thyroid gland at all -- they may just be suffering from iodine deficiency.
Seven Tips for Avoiding Bromine and Optimizing Iodine
Trying to avoid bromine is like trying to avoid air pollution -- all you can do is minimize your exposure. That said, here are a few things you can do to minimize your risk:
1. Eat organic as often as possible. Wash all produce thoroughly. This will minimize your pesticide exposure.
2. Avoid eating or drinking from (or storing food and water in) plastic containers. Use glass and safe ceramic vessels.
3. Look for organic whole-grain breads and flour. Grind you own grain, if possible. Look for the "no bromine" or "bromine-free" label on commercial baked goods.
4. Avoid sodas. Drink natural, filtered water instead.
5. If you own a hot tub, look into an ozone purification system. Such systems make it possible to keep the water clean with minimal chemical treatments.
6. Look for personal care products that are as chemical-free as possible. Remember -- anything going on you, goes in you.
7. When in a car or a building, open windows as often as possible, preferably on opposing sides of the space for cross ventilation. Utilize fans to circulate the air. Chemical pollutants are much higher inside buildings (and cars) than outside.
Avoid Unfermented Soy
Another major contributor to thyroid dysfunction that I did not discuss above is unfermented soy. Soy isoflavones can wreak havoc on your thyroid.
Kaayla Daniel's groundbreaking book, The Whole Soy Story: The Dark Side of America's Favorite Health Food is a powerful exposé that reveals the truth about the soy myths that have infiltrated our culture.
It's ironic that soy has become so accepted as a health food when, as Dr. Daniel states, thousands of studies link soy to malnutrition, digestive distress, immune-system breakdown, thyroid- and hormonal dysfunction, cognitive decline, reproductive disorders and infertility--even cancer and heart disease.
So if you want to keep your thyroid healthy, you'll definitely want to avoid unfermented soy products of all kinds, including soy milk.
a lot, no doubt. But hey, there are medications for that & in case the medication does not work we can add another which may or may not boost the effects of the primary medication, that is if you don't fall victim to one or more of the numerous side effects which may include death. From link:
Diagnosis of bromism is often difficult due to the protean manifestations of bromism, and physicians' failure to consider bromism as a cause of illness. Above all, diagnosis requires "clinical suspicion"--that is, the physician must consider the diagnosis or it will be missed.
It is concluded that the relatively low doses and short duration of bromide administration in PGW veterans, and the usually self-limiting nature of bromism, which normally abates following discontinuation of bromide-containing substances, suggest against bromism as a significant cause of ongoing illnesses in PGW veterans.
Psychiatric symptoms may include, in the earlier stages, disinhibition, self-neglect, fatigue, sluggishness, impairment of memory and concentration, irritability or emotional instability, and depression. Symptoms of more advanced disease may include confusion but occasionally schizophrenic-like psychotic behavior or hallucinations in clear consciousness. Behavior may become violent, especially at night. There may be severe auditory or visual hallucinations, or both. There may be clouding of consciousness, including stupor and coma (Horowitz, 1997; Fried and Malek-Ahmadi, 1975; Wacks, Oster, et al., 1990; Carney, 1973).
Neurological abnormalities of "all kinds" occur, including headache, tremor, slurred speech, spontaneous movements, incoordination, ataxia (abnormal gait), tendon reflex changes (increased or decreased reflexes), and extensor plantar responses (abnormal reflexes that signify "upper motor neuron" disease, disease in the brain or spinal cord that affects nerve signaling to the muscles) (Horowitz, 1997; Fried and Malek-Ahmadi, 1975; Wacks, Oster, et al., 1990; Carney, 1973). Vision changes have included decreased visual acuity often in conjunction with enlarged and poorly reacting pupils; disturbances of color perception, photophobia (abnormal sensitivity to light), micropsia and macropsia (perception of things as smaller or larger than they are), blurring of vision, and the quite characteristic mydriasis (enlarged pupils) (Levin, 1960; Kunze, 1976).
EEG: Generalized slowing of the EEG has been reported (Carney, 1973).
Dermatologic: Some patients will develop "bromoderma," an acne-like "papular" (raised) eruption of the face and hands (Horowitz, 1997; Wacks, Oster, et al., 1990); a "macular" (nonraised) rash may also be seen (Carney, 1973). In one case series, four of six bromism patients had abnormal pigmentation, usually of the sun-exposed areas (Carney, 1973).
Acute bromism is seldom seen because the bromide ion is irritating to the GI tract and produces vomiting before sufficient blood levels can be reached to cause bromism from short-term use. However, chronic bromism may develop--bromide is excreted slowly through the kidney, giving it the opportunity to build up in the body through ongoing ingestion (Morgan and Weaver, 1969).
Bromism was substantially more common prior to removal from the market of certain over-the-counter remedies high in bromide, such as Bromo-Seltzer and Miles Nervine (Wacks, Oster, et al., 1990); it was particularly common in the 1930s and 1940s but is substantially less so since the 1970s. Because of its relative rarity, physicians are less likely to consider bromism in the differential diagnosis, so that many cases may remain undiagnosed or misdiagnosed (Horowitz, 1997). One report observes that in almost every case report in the literature, including their own, the diagnosis of bromism was delayed while other causes of illness, including acute psychiatric or neurological illness, were considered (Horowitz, 1997). Another observes that "Perhaps because he regards it as extinct, the family doctor almost invariably fails to recognize bromism, even when, as in four of my (six) cases, he was the source of the supply" (Carney, 1973).
In the presence of clinical suspicion (typically arising from signs or symptoms of neurological or psychiatric disturbance without other identified cause), (1) a careful review of prescription and over-the-counter medications should be undertaken to elicit use of medications that may contain bromide. A dietary history may also be helpful; one report has implicated excessive consumption of colas containing brominated vegetable oil (Horowitz, 1997). Absence of identification of bromide-containing agents should not thwart further inquiry, as in some instances the source of bromide is never determined (Battin and Varkey, 1982); for this reason it has been suggested that bromide intoxication be considered "in the differential diagnosis of obscure, unusual, or refractory psychiatric symptomatology" (Battin and Varkey, 1982). (2) A chemistry panel should be obtained to evaluate presence of hyperchloremia, which may occur in the absence of a negative anion gap (Horowitz, 1997), and to allow calculation of the anion gap (Wacks, Oster, et al., 1990; Horowitz, 1997). Where suspicion directs, (3) serum bromide level should be secured (Wacks, Oster, et al., 1990). A serum bromide concentration above 50 mg/dL is considered confirmatory (Carney, 1973), and significant symptoms usually do not occur below this level (but see section on "Low-Level Bromism," below).
Cases of bromism have been reported with consumption of bromide-containing prescription and nonprescription medications, including PB in one reported case (in a patient with myasthenia gravis, receiving longer duration and higher-dose treatment than PGW veterans) (Wacks, Oster, et al., 1990), sleeping medications, and tonics; with consumption of cola that contains brominated vegetable oil; and with consumption of bromide-tainted well water (Fried and Malek-Ahmadi, 1975).
Most cases represent one of three groups: organic bromides, bromoureides, and biotransformation of bromide compounds (Horowitz, 1997). "Organic bromides" include the salts of sodium, potassium, and ammonium bromide; these salts have been available since 1857, with wide use during the 1930s and 1940s as sleep aids and antiepilepsy drugs (Horowitz, 1997). In 1938, bromide sales in the United States were surpassed only by sales of aspirin (Horowitz, 1997). However, many patients admitted to psychiatric institutions were found to suffer from bromism from overuse of these products, rather than from the psychiatric illnesses for which they had been incorrectly diagnosed, and the use of these products thereafter decreased until they were withdrawn from the market in 1975. Widely cited culprits included the sedative Nervine, produced by Miles Laboratory, which contained all three bromide salts; and Bromo-Seltzer, which contained 3.2 milliequivalents per teaspoon (mEq/tsp) of sodium bromide (Horowitz, 1997). Since these agents were withdrawn from the market, bromism has been far less frequent. "Bromoureides" are sedative-hypnotics available primarily in Europe, including Bromisovalum (Bromural) and carbromal (Carbitral) (Horowitz, 1997). Occasional reports of bromism from long-term overuse have been reported (Maes, Huyghens, et al., 1985). Finally, of particular relevance here, bromide released through the "biotransformation" of medications containing the bromide ion is an infrequent cause of bromism. PB and dextromethorphan bromide (used in cough medicine) have been reported to cause bromism. Anesthesia with the agent "halothane" will increase bromide levels, peaking at two to three days postanesthesia. Pesticide residues from common agricultural fumigants, such as "methyl bromide" and "ethylene dibromide," may elevate the bromide content of vegetables, but bromide toxicity has not been reported from this source (Horowitz, 1997).
Regional cerebral blood flow, that is, blood flow to different parts of the brain, may also be altered with bromism. Regional cerebral blood flow was assessed in a case of bromide psychosis using radioactive xenon (133Xe) inhalation (Berglund, Nielsen, et al., 1977). On the first exam, when the serum bromide level was 45 mEq/L (extremely high, within the potentially lethal range), the cerebral blood flow was reduced to approximately one-third of normal, with abnormal regional flow characterized by low flow in regions of the cortex, including frontal and parieto-occipital regions. Dialysis led to improvement in the clinical condition, and restoration of regional cerebral blood flow (Berglund, Nielsen, et al., 1977). Changes in regional cerebral blood flow--reflecting or perhaps influencing altered regional neuronal activity in the brain--could relate to symptoms of bromism.
|mg/dL||mEq/L = mmol/L||Toxicity|
|< 50||< 6.3||"Therapeutic"|
|100-200||12.5-25||Usually serious toxicity|
SOURCE: Ellenhorn, Schonwald, et al., 1997.
Of note, chronic use of bromide-containing drugs may result in serum bromide levels capable of interfering with chloride measurements without causing signs or symptoms of overt bromide toxicity. In one reported case of a myasthenic patient taking a total daily dose of 360 mg of PB (four times the daily PGW dose, and 110.4 mg bromide per day) (Wacks, Oster, et al., 1990), this measurement problem occurred. The patient was admitted with symptoms of myasthenia (but no symptoms of bromism). The abnormal anion gap was noticed in the course of evaluation of the patient for symptoms of reduced muscle strength, facial weakness, and slurred speech, compatible with myasthenia undertreatment or overtreatment. Serum bromide was 8.1 mEq/L (64.8 mg/dL).
A double-blind study has been performed in which several subjective and objective outcomes were evaluated following three months of bromide administration. Men and women receiving 0, 4, or 9 mg/kg/d of bromide (seven subjects in each group) for 12 weeks reported decreased ability to concentrate and increased sleepiness (among men only) who received bromide; and a statistically significant increase in several measures of thyroid function (among women only) (Sangster, Blom, et al., 1983). Mean plasma bromide at the end of treatment was 0.08, 2.14, and 4.30 mEq/liter in males; and 0.07, 3.05, and 4.93 mEq/liter for females, for the 0, 4, and 9 mg/kg/d groups, respectively. (The conversion is 8 mg/dL for 1 mmol/L, or 1 mEq/L). No changes were observed in measurements of hormones produced in the adrenals, the gonads, and the pituitary gland (Sangster, Blom, et al., 1983).
Of note: A study in rats found a significant decrease in thyroid function among female rats. Other rodent studies have reported (1) that bromide behaves more like iodine than like chlorine in the thyroid (iodine administration can induce hypo- or hyperthyroidism); and (2) that bromide can produce changes in thyroid hormones T4 and T3, in the absence of changes in thyroid-stimulating hormone (Vobecky and Babicky 1994; Vobecky, Babicky, et al., 1996a; Vobecky, Babicky, et al. 1996b; Velicky, Titlbach, et al., 1997a; Velicky, Titlbach, et al., 1997b; Velicky, Titlbach, et al., 1998). In humans, the action of PB in particular on thyroid-related hormones is well known, and PB is used in testing of certain thyroid hormone responses. It ordinarily enhances the release of a pituitary hormone, thyroid-stimulating hormone, in response to administration of a hypothalamic hormone, thyrotropin-releasing hormone (Coiro, Volpi, et al., 1998).
Several studies have cited instances of bromide toxicity at doses of serum bromide under those usually viewed as toxic (Sayed, 1976; Gerner, 1978), as low as 25 mg/dL (Battin and Varkey, 1982). Individual susceptibility varies greatly and it has been suggested that following prolonged intoxication serum levels may not accurately reflect nervous system involvement. (However, prolonged intoxication was quite unlikely to have characterized the PGW experience.) Moreover, toxic states may depend more on other factors. Suggested factors include the "general mental state," "premorbid personality" (both may be reflections of prior neurochemical state), duration of ingestion, state of hydration, and electrolyte balance of the patient (Battin and Varkey, 1982; Whybrow and Ewing, 1966; Freedman, Kaplan, et al., 1978)).
TIME-COURSE OF RESOLUTION OF BROMISM
The untreated half-life of bromide (time for half the initial blood amount to be excreted) administered orally is approximately 12 days (Vaiseman, Koren, et al., 1986); the half-life with saline is several days (about 65 hours), and a half-life as low as one hour has been reported with hemodialysis (see section on "Treatment"). Evidently there is no "slowly exchangeable" pool of bromide (bromide sequestered somewhere in the body where it is not readily eliminated); rather all bromide appeared to be "easily exchangeable" because adding a small amount of radiolabeled bromide (Br82) in a case of severe chronic bromide intoxication showed rapid and apparently complete equilibration of the stable and radioactive bromide (Blumberg and Nelp, 1966). The plasma-specific activity (radiolabeled bromide in counts per minute, or "cpm," divided by fraction of unlabeled bromide in mEq) remained constant as the plasma bromide decreased, and the bromide space (volume of distribution in liters) remained approximately constant).
Most reported cases resolve promptly with treatment of bromism through saline diuresis (sodium chloride delivery with enhanced urination) or hemodialysis. However, several reports indicate instances of partial resolution with long-lasting sequelae (see section on "Long-Term Symptoms").
Several case reports of bromism have noted the presence of persistent symptoms attributed to bromism that lasted beyond the time of elevated blood bromide levels.
Such case reports are rare, and it is difficult to exclude the possibility of concurrent pathology leading to persistent symptoms. That is, the residual symptoms, associated with observed cerebral atrophy, a seizure disorder, and a history of head trauma in the second case, could have had an independent cause. Neither can one exclude an effect or interaction of bromide with other drugs given prior to or during treatment, including in these instances the treatment agents clomethiazol or mercaptomerin. However, persistent effects resulting from bromism must be considered a possibility. Long-term effects from chronic regional cerebral blood flow abnormalities or from chronic chloride ion channel alterations (see "Causes of Bromism," above) could be hypothesized to relate to persisting effects. It is conceivable, but certainly not demonstrated, that prolonged hypoperfusion of selected brain regions with ongoing bromide intoxication could engender permanent changes, perhaps with frank loss of neurons or supporting glia, or reduction in synaptic contacts. It is also possible that chronic substitution of bromide for chloride could affect chloride channel behavior in the CNS, with consequent altered neurotransmission, leading to compensatory changes in neurotransmitter regulation. Still, such changes would be unlikely to be produced with short-term use of relatively low doses of bromide, such as occurred in PGW veterans taking PB.
Persistent Symptoms Following Bromisovalum
Bromisovalum has been reported to cause toxic symptoms, which in some instances are prolonged or permanent. In one series of eight cases with persistent symptoms, initial bromide levels were 105-169 mg/dl (with a mean of 140 mg/dl) (Harenko, 1967). The principal symptom was gait ataxia in all cases, with difficulty maintaining balance and staggering (8/8); then dysarthria (difficulty producing the muscle actions of speech) (6/8), exaggerated deep tendon reflexes of lower limbs (4/8), nystagmus (1/8), positive Babinski reflex (a pathological reflex) (1/8), tongue deviation to one side (1/8), and auditory impairment (Harenko, 1967). Changes in the eye, as seen with an ophthalmoscope ("fundal" changes), and impaired vision had been previously reported as irreversible lesions caused by bromisovalum, but were not encountered in these cases. Compared to patients who achieved complete recovery from bromisovalum poisoning, no differences were established in age, sex, duration and degree of abuse, prior illness, serum bromide level, symptoms, and severity of the subacute phase. Factors speculated to predispose individuals to persistent symptoms were recurrence of severe intoxication states, poor nutritional and general condition, and overlong continuance of the toxic condition (Harenko, 1967). It has been suggested that persisting symptoms with bromisovalum may result not from bromide ion or bromisovalum itself, but from 3-methylbutyrylurea (a breakdown product) or its metabolites (Harenko, 1967). Nonetheless, similarities between symptoms with bromisovalum toxicity and with bromide intoxication are sufficient for a common mechanism to be operative.
It is not possible to exclude a role for bromide in the two cases with symptoms that persisted long after elevated blood bromide levels would be presumed to be normal (or in the cases of prolonged symptoms with bromisovalum); nonetheless, these reports are rare and occurred in patients who ingested bromide at high doses for prolonged periods. Therefore, their experiences cannot be presumed to extend to PGW veterans who experienced low doses of bromide for brief periods.
In clinical reports of bromism, symptoms have generally cleared quickly with clearance of bromide; exceptions have typically involved chronic use with high doses and perhaps repeated toxicity. The relatively long half-life of bromide in the absence of treatment for bromism (approximately 12 to 14 days) remains quite short in comparison to duration of symptoms reported by many veterans. Even extreme bromism would be expected to resolve spontaneously in a month or two after bromide-containing agents are discontinued; and myasthenics taking substantially higher doses of PB (e.g., 12 times as high) for much longer times have seldom been reported to experience bromism, even when serum bromide levels were elevated and anion gaps modified. In contradistinction to the acetylcholinergic effects of PB, which might be expected to differ for myasthenics and PGW veterans, no reason has been identified that would suggest that bromide metabolism should differ systematically between myasthenics and PGW service personnel. Thus, although it is conceivable that experience with a much larger population, as seen in the PGW, would unveil a hitherto unrecognized longer-term syndrome at low doses, it would be expected to affect a relative minority of subjects reporting continued illnesses following participation in the PGW.
If studies on drug-drug or drug-chemical interactions are undertaken, using drug and chemical exposures in the PGW, addition of bromide to study regimens may be considered. (This may assist in unraveling relative contributions of AChE inhibition and bromide, if effects appear to involve PB as an interactant.)
Compatible symptoms? Some ill veterans report some neuropsychiatric symptoms crudely compatible with symptoms of bromism
Compatible relation of exposure to symptoms? Exposure to PB for longer durations and at higher doses would be more likely to produce bromism; however, seldom was the cumulative dose of PB received sufficient for production of bromism by our current understanding of bromism from decades of former use of bromide-containing agents. Disappearance of symptoms with a defined time-course after discontinuation of PB would be expected if bromism were the cause. This resolution of symptoms has not been widely reported. Thus, dose and time-course of exposure, and the relation to existence and time-course of illnesses, do not favor bromism as a cause.
Cases of persistent symptoms attributed to bromism: In one case, a 40-year-old woman initially showed "typical symptoms and signs of chronic bromide intoxication," including psychiatric symptoms, such as irritability and lethargy, a 30-pound weight loss, hand tremor, and minor gait difficulties while taking about 5 gm per day of bromdiathylacetylcarbamid as a sedative (Kunze, 1976). She developed a delirious state (fluctuating mental function) when the bromide-containing drug was stopped by a physician. (Such transient delirium has been not infrequently reported with bromide discontinuation.) Although the psychiatric symptoms cleared rapidly, the neurological state deteriorated; the most severe neurological state appeared 8 to 10 days after the drug was stopped, including a resting tremor of the head and upper extremities and a marked cerebellar dysfunction with severe generalized incoordination (ataxia) but without nystagmus. (Nystagmus is a rhythmic oscillation of the eyeballs that occurs, for a few cycles, with gaze far to one side, but is prolonged with some kinds of nervous system dysfunction.) The patient received a drug called Clomethiazol during this period, but no other CNS-toxic drugs, and all neuropsychiatric symptoms were assumed to result from bromism and the cessation of the bromide containing agent. A year after discharge from the hospital, despite some initial improvement, the patient was left with a mild dysarthric speech (altered speech production caused by difficulty performing the muscle movement involved in speech), a mild gait ataxia, and a moderate ataxia of her upper extremities so that writing was almost impossible. She had a marked constriction of her visual fields (that is, a loss of peripheral vision) which could be verified by formal testing (Kunze, 1976).
In the second case, a 60-year-old woman who had taken at least four teaspoons daily of triple bromide elixir for seven years, prescribed for a post-head-injury seizure condition, was hospitalized with bizarre behavior and hallucinations and a serum bromide concentration of 44.6 mEq/l. She was treated with isotonic saline and daily injections of mercaptomerin sodium (Thiomeri), but even after serum bromide levels fell to below 4 mEq/L and her mental state improved considerably, a significant deficit in orientation and memory remained. A pneumoencephalogram showed bilateral cerebral atrophy, which was presumed responsible for the residual abnormalities.
This reminded me about how salt helps bromine detox symptoms -- chloride cuts down the time it takes to eliminate what's been loosened.
"The chloride ion from sodium chloride competes with and replaces the bromide ion throughout the body. While the usual half-life of bromide (the time for half the body's complement of bromide to be eliminated) is 12 to 14 days (Horowitz, 1997), a half-life of 65 hours has been calculated with saline loading."