Below are the first 10 and last 10 pages of uncorrected machine-read text (when available) of this chapter, followed by the top 30 algorithmically extracted key phrases from the chapter as a whole.
Intended to provide our own search engines and external engines with highly rich, chapter-representative searchable text on the opening pages of each chapter. Because it is UNCORRECTED material, please consider the following text as a useful but insufficient proxy for the authoritative book pages.
Do not use for reproduction, copying, pasting, or reading; exclusively for search engines.
OCR for page 169
Multiple Chemical Sensitivities: A Workshop Considerations for the Diagnosis of Chemical Sensitivity William J. Rea Alfred R. Johnson, Gerald H. Ross, Joel R. Butler, Ervin J. Fenyves, Bertie Griffiths, and John Laseter INTRODUCTION The study of the effects of the environment upon the individual is now feasible due to new technology developed in the construction of environmental units.1,2,3. Our observations reveal that individual or multiple organs may be involved. The brain is the target organ in only a subset of chemically sensitive patients, and its involvement should not be confused with psychosomatic disease. Over the last 16 years physicians and scientists at the Environmental Health Center in Dallas have had an opportunity to observe over 20,000 patients who had chemical sensitivity problems. These patients were studied under various degrees of environmental control. This experience is unique in the world and has resulted in numerous peer-reviewed scientific articles, chapters in books, and books on this subject. Studies have resulted in over 32,000 challenge tests by inhalation, oral, or injection methods, of which 16,000 are double-blind. Blood chemical levels and fat biopsies for organic hydrocarbons number over 2,000, while the measurement of immune parameters are over 5,000 tests. Objective brain function tests have been accomplished in over 5,000 patients. Other objective tests, like computerized balance studies, depollutant enzyme levels, and autonomic nervous system changes as measured by the Iriscorder, number near 1,000. We wish to share our findings with the participants of the National Academy of Sciences Committee for the study of chemical sensitivity. DEFINITION AND PRINCIPLES Chemical sensitivity is defined as an adverse reaction to ambient doses of toxic chemicals in our air, food, and water at levels which are generally accepted as subtoxic. Manifestation of adverse reactions depend on: (1) the tissue or organ involved; (2) the chemical and pharmacologic nature of the toxin; (3) the individual susceptibility of the exposed person (genetic make-up, nutritional state, and total load at the time of exposure); (4) the length of time of the exposure; (5) mount and variety of other body stressors (total
OCR for page 170
Multiple Chemical Sensitivities: A Workshop load) and synergism at the time of reaction. (6) the derangement of metabolism that may occur from the initial insults. To demonstrate cause-and-effect proof of environmental influence on an individual's health, one must understand several important principles and facts. These principles involve those of total body load (burden), adaptation (masking, acute toxicological tolerance), bipolarity, biochemical individuality. Each principle will be discussed separately. TOTAL BODY LOAD (BURDEN) This is the patient's total pollutant load of whatever source (usually from air, food and water or surroundings1,2,4. The body must cope with this total burden; usually it must be utilized, expelled or compartmentalized. Total body load includes: (1) physical factors (e.g. hot, cold, weather changes, positive ions.5 electromagnetic phenomena.6 radon); (2) toxic chemicals (e.g. inorganics: Pb, Cd, Hg, A1, Br, etc.; organics: pesticides, formaldehydes, phenols, car exhausts, etc.).7-21 (3) biological (bacteria, virus, parasites, molds,22 food.)23,24 (4) psychological or emotional factors also significantly affect the patient, confirmed by recent work in psychoneuroimmunology, linking the psyche and the neuroendocrine and immune systems.25,26,27,28 Failure to reduce the total body load prior to pollutant challenge will frequently yield inaccurate results. Accordingly, we believe it is essential to conduct investigative procedures in controlled environmental circumstances with the total load reduced. ADAPTATION (MASKING, ACUTE TOXICOLOGICAL TOLERANCE) Induced by the internal or external environment, this is a change in the homeostasis (steady state), of body function with adjustment to a new "set point."29,30,31,32 Adaptation is an acute survival mechanism in which the individual "gets used to" a constant toxic exposure in order to survive, at the same time suffering a long-term decrease in efficient functioning and perhaps longevity. Selye was among the first to describe this compensatory mechanism.33 Because of adaptation or tolerance, the patient's total body load may increase undetected because the perception of a cause-and-effect relationship is lost. With no apparent correlated symptoms, repeated exposures may continue to damage his immune and enzyme detoxification systems. 34,35 The eventual result of continued toxic exposure over a period of days, weeks, months to years is end-organ failure.21 Withdrawal or avoidance of an offending substance for at least four days will aid in reducing the total body load, after which a controlled re-exposure challenge will reproduce cause-and-effect reactions. In these deadapted individuals, there is high reproduciblity of these evoked reactions permitting the physician to acquire sound scientific information. 36 BIPOLARITY After an exposure, the body initially develops a bipolar response of a stimulatory phase
OCR for page 171
Multiple Chemical Sensitivities: A Workshop followed by a depressive phase,37,29,1 usually with induction of immune and enzyme detoxification systems.38 If the incitant is strong enough, or if substantial size or duration of exposure occurs, the induced enzyme and immune detoxification systems are depleted or depressed by overstimulation and overutilization. An individual may also initially experience a stimulatory reaction in the brain, perceiving the inciting substance not as being but as actually producing an energizing "high". Therefore, he continues to acquire more exposures. After a period of time, however, be it minutes, months, or years, his body's defenses are adversely overstimulated and he develops disabling depression-exhaustion symptoms.31 This stimulation and depression-exhaustion pattern has been observed with many pollutant exposures, including ozone.30,12 When studying the effects of pollutants upon adapted individuals, the stimulatory phase is often missed or misinterpreted as being normal, thus giving faulty data. Studies in the controlled environment, involving 16,000 challenges in 2,000 deadapted patients, has proven this bipolarity phenomenon repeatedly. BIOCHEMICAL INDIVIDUALITY Another principle necessary to understand environmental aspects of health and disease, and especially chemical sensitivity, is that of biochemical individuality. Biochemical individuality of response is the individual's uniqueness.39 This uniqueness of response depends on the differing quantities of carbohydrates, fats, proteins, enzymes, vitamins, minerals, immune and enzyme detoxification parameters with which an individual is equipped to handle pollutant insults. These variations determine an individual's ability to process the noxious substances he encounters. They further contribute to the intensity of his reaction to toxic exposures and to his susceptibility to chemical sensitivity. Thus, a group of individuals may be exposed to the same pollutant. One person may develop arthritis, one sinusitis, one diarrhea, one cystitis, one asthma, and one may remain apparently unaffected. We have differing quantities and interactions of carbohydrates, fats, proteins, enzymes, vitamins, minerals, and immune parameters with which to respond to environmental factors. One simple example is the noted relationship between low serum magnesium levels and the HLA B35 genotype.40 This biochemical individuality allows us to either clear the body of noxious substances, or to collect them and contribute to the body burden. Biochemical individuality is dependent on at least three factors: genetic endowment, the state of the fetus's nutritional health and toxic body burden during pregnancy, and the individual's present toxic body burden and nutritional state at the time of exposure. Some individuals, for example, are born with significantly lower quantifies of specific enzymes (it may be 75%, 50% or even 25% of the norms). Their response to environmental stimuli is often considerably weaker than those born with 100% of the normal detoxifying enzymes and immune parameters. Examples are the babies with phenylketonuria or the individuals with transferase deficiency, who do well until exposed to their environmental triggers, and then damage sets in. There are over 2,000 genetically-transmitted metabolic errors, suggesting that most of the population will have at least one abnormality.41 Toxic volatile organic chemicals have been shown by Laseter to bioconcentrate in the fetus, increasing the acquired burden in some babies.42 It is well known that some individuals acquire their toxic load at work or around their homes.42 This changes with different seasons and weather conditions thus giving variable effects and responses over time. Extreme care must be taken in evaluation of each patient, who may exhibit unique clinical responses due to his specific biochemical individuality. As
OCR for page 172
Multiple Chemical Sensitivities: A Workshop an example, it is well known that not all patients will exhibit every reported symptom associated with systemic lupus erythematosus (SLE). Similarly, each patient exposed to the same environmental pollutant will react with his or her unique complex of symptoms. Because this vital fact is misunderstood, many studies are flawed when the wrong signs and symptoms are assessed for that individual. SPREADING PHENOMENA Spreading is a secondary response to pollutants that can involve new incitants or new target organs. Spreading that involves new incitants occurs when the body has developed increased sensitivity to increasing numbers of biological inhalants, toxic chemicals, and foods at increasingly smaller doses. At this time, overload becomes so taxing that a minute toxic exposure of any substance may be sufficient to trigger a response or autonomous triggering my occur. For example, a person initially may be damaged by a pesticide and then eventually have his disease process triggered by exposure to a myriad of toxic chemicals and foods, such as phenol, formaldehyde, perfume, beef, lettuce, etc. Spreading may occur for many reasons. It may be due to a failure of the detoxification mechanisms—oxidation, reduction, degradation and conjugation—brought about by toxic overloading, or it may occur because of depletion of the enzyme or co-enzyme's nutrient fuels, such as zinc, magnesium, all B vitamins, amino acid, or fatty acid. This depletion may account for an increasing inability to detoxify and respond appropriately. The blood brain barrier or peripheral cellular membranes of the skin, lung, nasal mucosa, gastrointestinal or genitourinary systems may be damaged allowing previously excluded toxic and nontoxic substances to penetrate to areas that increase the risk of harm. Immune or pharmacological releasing mechanisms may become so damaged that they are triggered by many substances toxic, then non-toxic (such as food) in addition to the specific one to which they were intended to respond. It is well substantiated that antigen recognition sites may be disturbed or destroyed by pollutant overload. Hormone deregulation (feedback mechanisms) may occur allowing for still greater sensitivity. In contrast to patients who experience increased sensitivity to multiple triggering agents, some chemically sensitive patients may have one isolated organ involved in their disease process for years, only to have dysfunction spread to other organs as their resistance mechanisms break down. This kind of spreading from one to another or multiple end-organs enables the progression of hypersensitivity and the eventual onset of fixed named disease. SWITCH PHENOMENON The switch phenomenon is the changing of one end-organ response to another. This usually occurs acutely, but may occur over a much longer period of time. This phenomenon was first described by Savage in the 1700s. He observed that when mental patients were at their worst, they usually had a remission of their asthma or sinusitis. When they were better mentally and they were seen in the outpatient clinic, they had a much higher incidence of sinus and asthma problems. Randolph and most other environmentally oriented physicians have also observed this phenomenon. At the EHC-Dallas, we have observed similar occurrences in our patients and, in fact, take cognizance of this phenomenon when evaluating therapy outcome.
OCR for page 173
Multiple Chemical Sensitivities: A Workshop In observing thousands of controlled challenges in the environmental unit, we have seen the target organ responses of many of our patients switch to several different ones during a long (e.g., 24-hour) reaction. Often we have seen, for example, transient brain dysfunction followed by arthralgia, followed by diarrhea, followed by arrhythmia. Therapy can appear to have been effective, even when a pollutant has not been totally eliminated. In this case, a new set of symptoms may begin indicating that a pollutant response has simply switched to another end-organ. This phenomenon occurs frequently when symptom-suppressing medication therapy or inadequate environmental manipulation is used. For example, a patient may have his sinusitis cleared by medication (e.g., cortisone). but later, since the cause has not been eliminated, he may develop arthralgia and eventually arthritis, or his colitis may have cleared only later to have cystitis develop. This life-long progression of disease does not have to occur if the switch phenomenon is recognized during initial evaluation. To prevent it, individuals and physicians need simply to be cognizant of seemingly unrelated events. For example, statements are often made to the effect that a child will outgrow a problem when, in reality, one symptom complex dissipates only to be replaced by a new set of symptoms. For example, a child may have recurrent ear infections. Eventually, these may stop, but bedwetting may ensue. Over time the bedwetting may cease, but the child may then develop asthma. These changes in health may appear to be totally unrelated; in this instance, however, they are switch phenomena. The situation of an adult who sprays pesticides in his home, and then visits a neurologist with complaints of headaches and a rheumatologist with symptoms of arthritis is similar. Both the physician and the patient frequently fail to recognize the relevancy of these seemingly disparate symptoms as being part of a larger pattern needing further investigation. POLLUTION FACTS In order to accomplish concise studies of the chemical sensitivity phenomena, one must understand some facts about environmental pollutants. Modern technology's rapidly accelerating rate of growth has produced a wide variety of chemical products, that contribute to the total chemical environment. Recent studies show that nearly 50% of the global atmospheric pollutants are generated by man, (either isolated from natural products or synthesized), and the ubiquitous nature of the toxic chemical agents is widely appreciated.8,13,14 It has been estimated that more than 2,000 new chemical compounds are introduced annually, and that over 60,000 different organic chemicals are used commercially today. The widespread presence of hazardous chemicals has rendered critical the environmental sensitivity problems described by Randolph almost 40 years ago.43 While celebrated instances of gross contamination have long been the object of professional attention, only recently have literally thousands of synthetic chemical products, heretofore believed innocuous, been incriminated as agents of homeostatic dysfunction 14,11. Current data affirm the view that standard methods for the determination of chemical incitants may no longer be effective.7,8,36,1 With the finding that sensitivities can occur from subthreshold and picomolar quantifies of chemicals, has come the discovery that standard procedures, such as skin prick or scratch tests, often fail to demonstrate positive reactions which are otherwise verifiable. Recent literature confirms the harmful effects of chemical incitants, like formaldehyde,44,45 phenol,45,46 some pesticides,7 chlorine,47 and petroleum alcohol,48
OCR for page 174
Multiple Chemical Sensitivities: A Workshop Commonly encountered chemicals like glycine,9,49 DDT, toluene and turpentine,50,51,52 and drugs such as hydralazine have been found to induce advanced-staged disease process.53 A number of familiar metals have also been incriminated, among them nickel, cobalt, chromium,54 aluminum,55 mercury,56 and platinum.57 Other common environmental chemical incitants include xylene,58 various acrylates,59 and acrylated prepolymers,60 benzyl peroxide, carbon tetrachloride,61 sulfates,62 dithiocarbamates,63 and diisocyanates. 64 WATER POLLUTION Water has an important role in delivering contaminant minerals, toxic organic and inorganic chemicals, particulate matter and radiation to the human organism. In developed nations, the incidence of many chronic diseases, particularly cardiovascular disease, is associated with water characteristics, like purity and mineral content.13 Hardness, or the lack thereof, is involved in heart disease, hypertension, and stroke.13 Among the theorized protective agents found in hard water are calcium, magnesium, vanadium, lithium, chromium and manganese. 13 Certainly, once cardiovascular pathology is induced, waters with high sodium content may be harmful. Other adverse agents include the metals cadmium, lead, copper, and zinc, which tend to be found in higher concentrations in soft water. Nitrates in water (usually from fertilizer) pose immediate threats to children under three months of age due to production of methemoglobin,65 and sulfur can also cause reactions in susceptible patients. City water, much of it secondhand, often contains from 100 to 10,000 times as many synthetic compounds as natural spring water.66 This, coupled with the rapid growth in the use of synthetic chemicals, has focused concern on the chemical quality of drinking water.13 Although microbes are important, attention is now being drawn to the microchemical contaminants. Advances in analytic chemistry has been able to reveal chemical contaminants in the parts-per-billion or parts-per-trillion range. It is a serious mistake to assume that extensive contamination of drinking water with "low" levels of synthetic pollutants is "normal." These chemicals are widespread, and we should not be lulled into assuming these contaminants are innocuous. Examination of our ground water has revealed many hundreds of toxic chemicals in these ranges.67,68 Many examples of water contamination exist and have been documented, including Times Beach, Missouri with winter floods flushing dioxin-contaminated oil used 20 years ago, Niagara's Love Canal area, Waterbury, Connecticut, and Middleboro, Kentucky.69 In many cases, deadly materials have been accumulating for years in dumps and landfills. In the United States, some 80,000 pits and toxic waste lagoons hold chemicals ranging from carbon tetrachloride to discarded mustard-gas bombs.68 Slowly escaping from their burial sites, these leftovers directly contaminate our ground water. Polluted ground water exists at 347 of the nations 418 worst chemical dumps, and probably is occurring in the rest.68 Laseter7 and others70 have shown that a virtual organic chemistry laboratory exists in most drinking water. In the early 1980s, California, New York, New Jersey, Arizona, Nova Scotia, and Pennsylvania condemned dozens of public water supply wells due to trichloroethylene or tetrachloroethylene pollution.71 Leaking fuel tanks contaminated nine Kansas public water supplies in 1981.71 Officials in New Mexico identified 25 cities where hydrocarbons and solvents contaminated the ground water.71 Analysis of New Orleans drinking water alone revealed the presence of 13 halogenated hydrocarbons.
OCR for page 175
Multiple Chemical Sensitivities: A Workshop Sources of water pollution fall into three major categories: (i) municipal sewage; (2) agricultural wastes; and (3) industrial wastes. Approximately 55% of the water treated in municipal plants is from homes, while another 45% is from industry. Agricultural wastes include those from livestock and toxic chemicals (pesticides, herbicides, fertilizers), and farm runoff collects in rivers, lakes, and ground water. Industrial wastes, however, contain some of our more toxic substances. Over one-half of the total volume of industrial wastes come from paper mills, organic chemical manufacturing plants, petroleum companies, and steel manufacturing. The major pollutants are chemical byproducts, oil, grease, radioactive waste and heat. Other sources of contamination are drinking water disinfectants and byproducts; 68 it should be remembered that chlorine, interacting with organic material, produces toxic trihalomethanes and other organochlorines. Alternatives to treating water with chlorine include ozone, chloramines, ultra-violet irradiation, iodination, or home reverse-osmosis and charcoal filtration.68 Chloride, added at many sewage treatment plants, can also react with organic matter in the water to form chlorinated hydrocarbons, many of which are also known to cause cancer. Copper sulfate, aluminum sulfate and fluorine are other major contaminants which may add to the total body burden.68 Over a thousand different toxic chemicals have been found in public water supplies including pesticides, herbicides, industrial solvents, and polychlorinated biphenyls, just to name a few. Inorganic pollutants include arsenic, cadmium, chromium, copper, manganese, mercury, silver, and selenium.13 The use of inorganic arsenic insecticides has lead to high arsenic levels ha some water supplies.13 Barium (greater than 1 mg/L) has toxic effects on the heart, blood vessels, and nerves,68 while cadmium at levels greater than .Olmg/L has adverse arterial effects. At levels greater than lmg/L or one ppm, the following metals found as water contaminants have produced severe chronic toxicity: antimony,72 beryllium,73 cobalt, 73 gold,73 iodine,73 lithium,73 mercury,74 and vanadium.73 In Minamata, Japan, between 1953 and 1960, various plastic companies dumped methyl mercury chloride into the water, producing 50 to 85 ppm of mercury ha nearby fish. Four hundred and six people died after ingesting these mercury-contaminated fish, and the adverse toxicological effects on developing children are continuing to be measured.75 A recently completed study found that skin absorption contributed from 29 to 91% of the total body dose of pollutants (from water), with an average of about 64%.76 This is even more important when one looks at the large number of volatile organic compounds found in our drinking and bath water. Radiation occurs in some waters in the form of radon, a naturally occurring radionuclide that seeps from rocks and may be concentrated in airtight homes, especially the basements. At this stage, more information is needed to fully assess its effects. It probably, however, can increase the total body load. In 1965, a serious drinking-water problem was seen in 40 percent of patients hospitalized for a program of comprehensive environmental control.1,77,78 Today it is up to 80%. We have found that patients susceptible to water contaminants virtually always exhibit multiple sensitivities, with advanced and severe environmental reactions, especially to airborne chemicals.1 Interestingly, water sensitivity in children was found to increase on a circadian and seasonal basis. 79 Increased severity was seen during June and July or in September and October, when grass, pollen, and mold counts were also high.79 Some ECU patients had difficulty with waters containing high levels of sodium, others with calcium, and still others with high bicarbonate waters. A few individuals tolerated distilled water, even
OCR for page 176
Multiple Chemical Sensitivities: A Workshop though it may contain some hydrocarbon residuals. Hundreds of outpatients have shown symptoms in reaction to both chlorinated and nonchlorinated waters, including numerous spring, charcoal-filtered, and distilled waters. If these water-induced symptoms remain undiscovered, food and chemical testing, may be distorted. It is vital to test and find safe water before proceeding with other testing in these severely sensitive individuals. CHEMICAL CONTAMINATION IN FOODS The contamination of our urban food supplies is the result of widespread use of food additives, preservatives, and dyes in growth, manufacturing and processing. Virtually all commercially grown and prepared foods have pesticides and herbicides in them.79,9 The literature abounds with reports of chemical sensitivities to many additives.80,81 Contaminant reactions complicate the study of food sensitivity, forcing one to define more dearly the nature of the incitant, not only as it is encountered in foods, but in the air and water as well. Bell has reported urticarial reactions and immunological changes to exposures to a number of food additives. 82 Condemi83 and Bell both suggest that food dyes may trigger reactions in sensitive individuals; including conditions commonly thought to be psychogenic, or certain forms of hyperreactivity.28,84,85,86,87,88,89 Lindemayer has associated urticarial reactions with several additives such as p-hydroxybenzoic acid propylester, benzoic acid, sodium benzoate, ponceau rouge, and indigo carmine.90 Monroe's data indicate a casual role played by tartrazine azo dyes and salicylates in the provocation of vascular alterations.36 Other additives, including sodium nitrite and sodium glutamate, have been found to trigger migraine phenomena in susceptible patients.91 Sulfur dioxide16 and sodium salicylate can provoke asthmatic reactions, 92 while aspirin-like food contaminants and dyes may trigger urticaria, angioedema, bronchoconstriction and purpura.93 An even wider variety of symptoms, including severe gastrointestinal disorders, has been associated with sensitivities to aniline, commonly found in rapeseed oil.94 In our experience, natural toxic components of foods, such as alkaloids, phenols lectins, etc. must also be accounted for when studying the secondary food sensitivity which occurs from pollutant overload in the chemically sensitive. Therefore, three factors must be considered when evaluating the total food load. These are man-made pollutant contamination, natural toxic effects of foods, and food sensitivity. Failure to consider all three in the chemically sensitive patient may color or negate otherwise a dearly defined case of chemical sensitivity. CHEMICAL INCITANTS IN THE HOME ENVIRONMENT Indoor air pollution in the home environment has produced a multitude of sensitivities to chemicals.8,95 Time and space limitations allow only a cursory review of the numerous commercial hygienic products which can be noxious for chemically susceptible individuals. Among these are a wide variety of cosmetics.96,97 particularly those containing glycerin, propylene glycol, or butylene glycol,98 perfumes,99 and hair products such as dyes,100,101 creams,102 sprays,103 and shampoo. 104 Moreover, sensitivities have been demonstrated to occur in association with lip salve,105 fingernail preparations,106 soaps,107 sanitary napkins,108 mouthwash,109 antiperspirants,110 contact lenses.111 contact lens solutions,112 and suntan lotions.113
OCR for page 177
Multiple Chemical Sensitivities: A Workshop Reports are widespread of sensitivities to chemicals in textiles, including synthetic acrylic fibers,114 polyester spin finishes,115 the epoxy resins, and synthetic clothing.116 Products such as fabric spray starch may also be considered toxic for the chemically sensitive individual117 for whom even the metallic buttons on blue jeans may trigger reactions to nickel.118 Formaldehyde44 on synthetics or tetrachloroethylene, from dry-cleaned clothing can also produce problems. Household cleaning products, particularly those containing formaldehyde, phenols and chlorine are hazardous for many patients. Several laundry products and detergents may be identified as household incitants119, as well as a number of products used to dean and polish furniture 120. The very construction of many homes may prove dangerous for the chemically sensitive patient. Data suggests that chemicals contained in wood preservatives (e.g., pentachlorophenols) are environmental incitants capable of triggering a variety of symptoms.121,122,123 Others report problems with reactions to formaldehyde-containing pressboard, carpets, plywood and petrochemical contaminants.124 Current data confirm earlier findings regarding the hazards of pesticides 125 such as 2,4,DNP and fungicides126. Moreover, research increasingly suggests the possibility of sensitivities to apparently innocuous items such as rubber bands,127 coins,128 epoxy,129 and countless paper products.130,131 Pesticides, along with oil, gas or coal are major offenders for sensitive individuals. Research shows house plants132,133 and common insects134 can now be viewed as environmental incitants or causes of homeostatic dysfunction. In addition, sensitivities to cold and heat,36 and to contaminants in household water supplies have been associated with symptoms ranging from urticaria to severe respiratory distress. Natural gas heat and stoves, and routine insecticiding or termite proofing of homes can be prime offenders in chemical sensitivity. One must consider these potential sources of contaminants when developing studies on chemical sensitivity. In our experience, failure to evaluate building and home environments before challenge testing will often make challenge studies invalid for the diagnosis of chemical sensitivity. MECHANISMS The mechanisms involved in chemical sensitivity are becoming clearer, one of which has pollutant injury occurring to the lungs or liver, with resultant free radical generation135. Disturbances then occurs at the cellular, subcellular and molecular levels, producing injury either immunologically, or nonimmunologically through enzyme detoxification systems. Vascular or autonomic nervous system dysfunction will then occur with one or a myriad of end-organ responses. IMMUNOLOGICAL Type I hypersensitivity is usually mediated through the IgE mechanism on the vessel wall. Classic examples are angioedema urticaria, and anaphylaxis due to sensitivity to pollen, dust, mold, or food,136 or some chemicals such as toluene diisocyanate. Ten percent of the patients with immunological involvement with chemical sensitivity seen at the ECH-Dallas seem to fall within this category.
OCR for page 178
Multiple Chemical Sensitivities: A Workshop Type II cytotoxic damages may occur with direct injury to the cell. A clinical example of this is seen in patients exposed to mercury 137. A group in Minimata, Japan developed neurological disease from eating fish exposed to toxic methyl mercury chloride. Mercurial pesticides fall into this category. Twenty percent of the patients with immunological involvement seen at the EHC-Dallas seem to fall into this Type H category. Type III shows immune complexes of complement and gamma globulin damaging the vessel wall. A clinical example of this is lupus vasculitis. Numerous chemicals, including procainamide and chlorothaizide, are known to trigger the autoantibody reaction of lupus-like reactions. Many other toxic chemicals can also trigger the autoimmune response 138. Other chemicals, such as vinyl chloride, will produce microaneurysms of small digital arterioles, probably due to this mechanism139,51. Type IV (cell-mediated) immunity occurs with triggering of the T-lymphocyte. Numerous chemicals such as phenol, pesticides, organohalides, and some metals will also alter immune responses, triggering lymphokines, and producing the Type IV reactions138. Clinical examples are polyarteritis nodosa, hypersensitivity angiitis, Henoch-Schonlein purpura, and Wegener's granulomatosis1,139. A recent study done at the Environmental Health Center-Dallas on 104 proven chemically-sensitive individuals (70 vascular, 27 asthmatic, and 7 rheumatoid), comparing them with 60 normal controls, showed that those manifesting a chemical sensitivity through their vascular tree had suppression of the suppressor T-cells (greater than 4 S.D.)47. Clearly the larger portion of our patients with immunological involvement fall into the Type III and IV categories. NON-IMMUNE ENZYME DETOXIFICATION Non-immune triggering of the cell and vessel wall may occur. Complement may be triggered directly by molds, foods, or toxic chemicals139, and mediators like kinins, postaglandins, etc. may also be directly triggered. These reactions then cause vascular spasm, with resultant hypoxia and release of lysozymes, which further produces more spasm, hypoxia, etc. Eventually end organ failure will occur. Triggering of the enzyme detoxification, mostly in the systems liver and respiratory mucosa, plays an important role in clearing of pollutants. It occurs, however, to a lesser extent in all systems. Foreign compound biotransformations have considerable variability, depending on genetic factors, age, sex, nutrition, health status, and the size of the dose. The metabolism of foreign compounds usually occurs in the microsomal fraction (smooth endoplasmic reticulum) of liver cells. A few biotransformations are non-microsomal (redox reactions involving alcohols, aldehydes and ketones). There are basically four biotransformation categories — oxidation, reduction, degradation, and conjugation. The first three biotransformation pathways for xenobiotics are the same pathways that the body uses to process food and nutrients. If these enzyme systems are over-utilized by competing foreign pollutants, inadequate handling of food proteins can result, with the subsequent induction of food sensitivities. However, because these detoxification pathways are dependant on nutrient and mineral cofactors, these systems are inducible by appropriate oral or systemic supplementation. Such supplementation serves as an important factor in stabilizing and treating patients with chemical sensitivity. The fourth category of biotransformation, that of conjugation, is almost exclusively for handling foreign compounds. Conjugation appears to be uniquely utilized for the catabolism of foreign compounds, using amino acids and their derivatives with peptide bonds, and carbohydrates and their
OCR for page 179
Multiple Chemical Sensitivities: A Workshop derivatives with glucide bonds. Simpler compounds like sulfate and acetate are also involved in conjugation with linkage of ester bonds. Activated conjugated compounds plus specific enzymes are often detoxified by coupling with co-enzymes, Examples: co-enzyme A with acetate, and other short-chain fatty adds adenosine or phosphoadenosine phosphate is detoxified with a methyl group from sulfate methionine, or the ethyl group from ethionine. Similarly, uridine and phosphate with glucose and glucuronic acids140,141. There are generally five major categories of foreign-compound conjugative processes140. These are: 1) acetylation through co-enzyme A, for detoxifying aromatic amines and sulfur amides; 2) peptide conjugation with glycine and aromatic carboxylic acids to hippuric acid; 3) sulfonation with glutathione (containing cysteine) or PAPS, and microsomal enzyme conjugation for multi-ring systems such as naphthalene, anthracene, and pheno-anthracene, which eventually results in benign mercaptic acids or alternatively benign sulfate esters; 4) alkylations by methionine of amines, phenols, thiols, noradrenalin, histamine, serotonin, pyridine, pyrogallol, ethylmucaptin sulfites, selenites and tellurites; 5) Glucuronation. Glucuronides detoxify pesticides, alcohols, phenols, enols, carboxylic acid, amino hydroxamines, carbamides, sulfonamide and thiol140,141. All of these processes are dependent upon nutrient fuels to keep these processes running efficiently. Toxic chemicals disturb the supply of the nutrient fuels by 1) producing poor quality food, 2) reducing intake, 3) reducing normal absorption, 4) setting up competitive absorption in the gut with nutrients, 5) imbalancing intestinal flora, 6) disturbing transport mechanisms, 7) disturbing proper decomposition and metabolism, 8) causing renal leaks, and 9) directly damaging nutrients. If nutrient inadequacy occurs, normal metabolism is overloaded and disturbed, resulting in selective changes in the pools of nutrients such as vitamins, minerals, amino adds, enzymes, lipids, and carbohydrates. Once this occurs, there is a viscous cycle of dysmetabolism, often with production or worsening of chemical sensitivity. These detoxification and metabolic defects are often measurable and have been accomplished in over 2,000 chemically sensitive patients. DIAGNOSIS The diagnosis of chemical sensitivity can now be made with a combination of the following history, physical examination, immune tests including IgE, IgG, complements, T & B lymphocyte subsets, blood levels of pesticides, organic compounds, heavy metals (intracellular), and occasionally objective brain function tests. Antipollutant enzymes, such as superoxide dismutase, glutathione, peroxidase, and catalase have been found to be suppressed in the chemically sensitive. Vitamin deficiencies, mineral deficiencies and excess, amino acid deficiency and disturbed lipid and carbohydrate metabolism has been observed. Challenge tests are the cornerstone of confirmatory diagnosis. These may be accomplished through oral, inhaled, or intradermal challenges. Care should be taken to rule out inhalant problems with pollen, dust, and molds. Food sensitivity occurs in approximately 80% of the people with chemical sensitivity; and must be evaluated. When diagnosing chemical sensitivity, one must investigate water contaminant sensitivities, as 90% of people with chemical sensitivity have water contaminant reactions4. This can be checked by placing the patient on less chemically-contaminated, charcoal filtered, distilled, or glass-bottled spring water for four days, with subsequent rechallenge of the patient's regular drink water. This procedure will often elicit a reaction to the water pollutants in the sensitive individual.
OCR for page 182
Multiple Chemical Sensitivities: A Workshop chemically contaminated water (including spring, distilled, and charcoal filtered), may be used, but only in glass or steel containers. Water will leach a variety of contaminants from the walls of synthetic plastic containers. A rotary diet of less chemically contaminated food, should also be used to reduce load and keep the patient in the unmasked state. Remove as many household incitants as possible, including petroleum-derived heat, insecticides, synthetic carpets and mattresses, and formaldehyde-containing substances such as pressboard and plywood. Toxic exposures can be monitored by the general volatile organic hydrocarbon blood tests. Some job changes may be needed, while occasionally the most severely affected patients have to leave badly polluted areas. Techniques should be developed for follow-up and monitoring of these modalities. Injection therapy for inhalants, foods, and some chemicals will also help this problem24,144,145,147,148,149,150. Low-dose sublingual therapy in patients with allergic rhinitis was effective151. These treatments can be done daily, but usually every four to seven days. In our opinion, a properly balanced rotary diet is essential in treating the patient with food sensitivity, whether or not it may be induced by chemical overload. Vitamin and mineral supplementation is often necessary to replace the deficiencies that occur from the direct toxic damage, exhausted enzymatic detoxification pathways, and from the direct competition absorption. In rare cases, nutritional replacement with intravenous hyperalimentation is needed for severely debilitated patients. Techniques should be developed for monitoring and evaluating the outcome. CONCLUSION The philosophy and techniques of environmental medicine developed over the last 25 years offers a means to scientifically investigate and treat patients affected by pollutants. This approach gives the physician valuable, accurate information, in the pursuit of optimum health for these environmentally-sensitive patients.
OCR for page 183
Multiple Chemical Sensitivities: A Workshop REFERENCES 1. Randolph, T.G., Human Ecology and Susceptibility to the Chemical Environment. Springfield, Illinois: Charles C. Thomas, 1962 (sixth printing 1978). 2. Dickey, L.D. (Ed.), Clinical Ecology. Springfield, Illinois: Charles C. Thomas, 1976. 3. Bell, I.R., Clinical Ecology. Bolinas, California: Common Knowledge Press, 1982. 4. Rea, W.J. and Mitchell, M.J. Chemical sensitivity and the environment. Immun Allerg Prac, Sept/Oct: 21-31, 1982. 5. Wordan, J.I. The effect of air in concentrations and polarity on the C02 capacity of mammalium plasma. Fed Proc 1954; 13:557. 6. Choy, R.V.S., Monro, J.A., Smith, C.W., Electrical Sensitivities in Allergy Patients. Clin Ecol Vol IV No. 3. pp. 93-102. 7. Laseter, J.L.; DeLeon, I.R.; Rea, W.J.; Butler, J.R. Chlorinated hydrocarbon pesticides in environmentally sensitive patients. Clin Ecol, 2(1):3-12, 1983. 8. National Research Council. Indoor Pollutants. Washington, D.C.: Natl. Academy Press, 1981. 9. Gilpin, A. Air Pollution, 2nd Ed. St. Lucia, Queensland: University of Queensland Press, 1978. 10. Wark, K. and Warner, C. Air Pollution: Its Origin and Control. New York: Harper & Row, 1961. 11. Adelman, R.C. Loss of adaptive mechanisms during aging. Fed. Proc. 38:1968-1971, 1979. 12. Stokinger, H.E. Ozone toxicology: A review of research and industrial experience, 1954-1962. Arch Environ Health, 110:719, 1965. 13. The National Research Council. Water hardness and health. In Drinking Water and Health. New York. National Academy of Science, 1977, 439-447. 14. Winslow, S.G. The Effects of Environmental Chemicals on the Immune System: Selected Bibliography With Abstracts. Oak Ridge, TN: Toxicology Information Response Center, Oak Ridge National Laboratory, 1981. 15. Calabrese, E.J. Pollutants and high-risk groups. The Biological Basis of Increased Human Susceptibility to Environmental and Occupational Pollutants. NY: Wiley
OCR for page 184
Multiple Chemical Sensitivities: A Workshop Interscience, 1977. 16. Freedman, B.J. Sulphur dioxide in foods and beverages: its use as a preservative and its effect on asthma. Br J Dis Chest, 74(2):128-134, 1980. 17. Davidson, M. and Fienleib, M. Disulfide poisoning:. A review. Am Heart J, 83:100, 1972. 18. Innami, S., Tojo, H., Utsuja, S.; Nakamura, A.; and Nagazama, S. PCB Toxicity and Nutrition I. PCB Toxicity and Vitamin A. Jap J Nutr, 32:58-666, 1974. 19. Villeneune, D.C., Grant, D.L., Phillipos, W.E.J.; Clark, M. L.; and Clegg, D. J. Effects of PCB administration on microsomal enzyme activity in pregnant rabbits. Bull Environ Contain Toxicol, 6:120, 1971. 20. Rea, W.J.; Johnson, A.R.; Smiley, R.E.; Maynard, B.; and Dawkins-Brown, O. Magnesium deficiency in patients with chemical sensitivity. Clinical Ecology, 4(1): 17-20, 1986. 21. Pan, Y., Johnson, A.J., Rea, W.J.: Aliphatic Hydrocarbon Solvents in Chemically Sensitive Patients. Clin Ecol 5(3):126-131,1987-88. 22. Olson, K.R., et al: Amanita phalloides-type mushroom poisoning. West. J. Med. (37:282, 1982). 23. Brostoff, Jonathan, and Challacombe Stephen; Food Allergy and intolerance, London, Bailliere Tindall/W.B. Saunders, 1987. 24. Rapp, O.J. Double-blind confirmation and treatment of milk sensitivity. Med J Aust. 1:571-572, 1978. 25. Rea, W.J.; Pan, Y. et al: Toxic Volatile Organic Hydrocarbons in Chemically Sensitive Patients, Clin Ecol 5(2):70-74,1987. 26. Hill, Johanna Peptides and Their Receptors as the Biochemicals of Emotion, proceedings of the American Acad. Envir. Med. Annual Mtg., Nashville, TN, Oct. 29, 1987. 27. Ader, Robert Behavioral Influences of Immunity, proceedings of Amer. Acad. Envir. Med. Annual Mtg., Nashville, TN, Oct. 29, 1987. 28. King, D.S. Can allergic exposure provoke psychological symptoms? A double-blind test. Biol Psychiat. 16:3-19, 1981. 29. Randolph, T.G. Specific Adaptation. Ann Allergy. 40:333-45, 1978. 30. Mustafa, M.G. and Tierney, D.F. Biochemical and metabolic changes in the lung with oxygen, ozone, and nitrogen dioxide toxicity. Am Rev Resp Dis, 118(6), 1978.
OCR for page 185
Multiple Chemical Sensitivities: A Workshop 31. Stokinger, H.E. and Coffin, D.L. Biological effects of air pollutants. In A.C. Stern (Ed.), Air Pollution. New York: American Press, 1968. 32. Rinkel, H.J.; Randolph, T.G.; and Zeller, M. Food Allergy. Norwalk, Connecticut: New England Foundation of Allergic an Environmental Disease, reprint of 1951 text. 33. Selye, H. The general adaptation syndrome and the diseases of adaptation. J. Allergy, 17:23, 1946. 34. Jollow, D.J., et al. 1977 Biological Reactive Intermediates: Formation, Toxicity, and Innetivation. New York. 35. Wand, A.M., et al. 1976 Immunological mechanisms in the pathogenesis of vinyl chloride disease. Brit. Meal. 1.1, 6015:936-938. 36. Rea, W2.; Peters, D.W.; Smiley, R.E. et al. Recurrent environmentally triggered thrombophlebitis. Ann Allergy, 47:338-344, 1981. 37. Savage, G.H. Insanity and Allied Neuroses. Philadelphia: Lea and Febiger, 1884. 38. Rowe, A.H. Allergic toxemia and migraine due to food allergy. Calif West Meal. 33:785-792, 1930. 39. Williams, R.J. Biochemical Individuality. New York: Wiley, 1963. 40. Noordhout, B., et al. ''Latent Tetany, magnesium and HLA tissue antigens.'' Magnesium-Bulletin 3 (offizielles organ Gesellshaft fur magnesium forsehung) 9, 3, 1987. 41. Stanbury, J.B., et al. The Metabolic Basis of Inherited Disease, 5th printing New York, McGraw-Hill Book Co., 1983. 42. Nadal, A. and Lee, L.Y. Airway hyperirritability induced ozone. In S.D. Lee (Ed.), Biochemical Effects of Environmental Pollutants. Michigan: Ann Arbor Science Publishers, 1977. 43. Randolph, T.G. Sensitivity to petroleum. Including the derivatives and antecedents. a. Lab Clin Med 40:931-932 Dec. 1952. 44. Fisher, S.A.: Dermatitis due to the presence of formaldehyde in certain sodium lauryl sulfate (SLS) solutions. Curtis 27(4):360-2, 366, Apr, 1981. 45. Fregert, S.: Irritant dermatitis from phenol-formaldehyde resin powder. Contact Dermatitis 6(7):493, Dec., 1980. 46. U.S. Environmental Protection Agency: Unfinished Business. A Comparative Assessment of Environmental Problems.
OCR for page 186
Multiple Chemical Sensitivities: A Workshop 47. Rea, W.J., Johnson, A.R., Youdim, S., Fenyves, E.J., Samadi, N. T. & B Lymphocytes. Parameters Measured in Chemically Sensitive Patients and Controls. 48. Mohave, L., Moller, J.: The Atmospheric Environment in Modern Danish Dewllings — Measurements in 39 Flats . Institute of Hygiene, University of Aarhus, Denmark. Paper presented at International Indoor Climate Symposium. Copenhagen, 1978. 49. Suhonen, R.: Contact allergy to dodecyl-di-(aminoethyl) glycine (Dedsimex i). Contact Dermatitis 6(4):290-1, Jun., 1980. 50. McMillian, R.: Environmentally-induced thrombocytopenic purpura, JAMA 242(22):2434-5, Nov. 30, 1979. 51. Rea, W.J.; Bell, I.R.; and Smiley, R.E., Environmentally triggered large-vessel vasculitis. In F. Johnson and J.T. Spence (Eds.), Allergy: Immunology and Medical Treatment. Chicago: Symposia Specialist, 1975. 52. Rea, W.J. Review of cardiovascular disease in allergy. In C.A. Frazier (Ed.), Biannual Review of Allergy. Springfield, Illinois, 1979-80. 53. Peacock, Al: Case reports, hydralazine-induced necrotizing vasculitis, Br Med J 282(6270):1121-2, April 4, 1981. 54. Dooms-Goossens, A., Ceuterick, A., Vanmaele, N., Degreef, H.: Follow-up study of patients with contact dermatitis mused by chromates, nickel, and cobalt. Dermatologica 160(4):249-60, 1980. 55. Clemmensen, O., Knudsen, H.E.: Contact sensitivity to aluminum in a patient hyposensitized with aluminum precipitated grass pollen. Contact Dermatitis 6(2):305-8, Aug., 1980. 56. Vermeiden, Oranje, A.P., Vuzevski, V.O.: Stolz, E. Mercury exanthem as occupational dermatitis. Contact Dermatitis, 6(2):88-90, Jan., 1980. 57. Hughes, E.G.: Medical surveillance of platinum refinery workers. Soc Occup Med 30(1):27-30, Jan., 1980. 58. Bell, I., King, D.: Psychological and physiological research relevant to clinical ecology: an overview of the recent literature, Clin Ecol, 1982. 59. Bjorkner, B., Dahlquist, I., Fregert, S.: Allergic contact dermatitis from acrylates in ultraviolet curing inks. Contact Dermatitis 6(6):405-9, Oct. 1980. 60. Bjorkner, B.: Sensitization capacity of acrylated prepolymers in ultraviolet curing inks tested in the guinea pig. Acta Derm Venercol (Stockh), 61(1):7-10, 1981. 61. Romaguera, Gimalt, Sensitization to benzoyl peroxide, retinoic acid and carbon
OCR for page 187
Multiple Chemical Sensitivities: A Workshop tetrachloride. Contact Dermatitis, 6(6):442, Oct., 1980. 62. Satish, J. Importance and measurement of sulfates in floating dust. Soz Praeventivmed 25(4):201-2, Sep., 1980. 63. Kleibl, K., Rackova, M.: Cutaneous allergic reactions to dithiocarbamates. Contact Dermatitis 6(5):348-9, Aug., 1980. 64. Gallagher, J.S., Tse, C.S., Brooks, S.M., Bernsten, I.I.: Diverse profiles of immunoreactivity in toluene diisocyanate (TOI) asthma. JOM 23(9):610-6, Sep., 1981. 65. Wilson C.W.M. Hyperreactivity to Maine tap water in children: its clinical features and treatment. Nutri and Health 2: 51-63, 1983. 66. Glaze, W.E., North Texas State University, Environmental Division, Denton, Texas, Personal communication. 67. Cherry, R. and Cherry, F.: What's in the water we drink? The New York Times Magazine, Dec. 8, 1974. 68. Environmental Protection Agency (EPA): Is your drinking water safe? (Booklet) 69. Trimble, J. U. S. News and World Report, Feb. 28, 1984, pp.27-32. 70. Spalding, R.F.; Junk, G.A. Richard, J.J. Water: Pesticides in ground water beneath irrigated farmland in Nebraska, Pesticides Monitoring Journal 1(2): 70-73, 1980. 71. Junk, G.A.; Spalding, R.F. and Richard, J.J. Aureal, Vertical, and temporal differences in ground water chemistry. II. Organic constituents, 1983. 72. Corwin, A.H. Heavy metals in air, water, and our habitat In Dickey, L.D. (Ed) Clinical Ecology, Springfield, II: Charles C. Thomas, 1976, pp. 292-305. 73. Moran, J.M.; Morgan, M.O. Wiersma J.N Introduction to Environmental Science 2nd Ed. New York: W.H. Freeman and company, 1986, pp. 177-209. 74. Skiba, N.S. Role of river discharge of solids in migration of mercury, Zap Kirgizsk Otd Vses Mineralog Obschchestva 4:31, 1963; Chem Abst, 61:5357e, 1964. 75. Takenchi, T. Morikawa, N.; Matsumoto, H.; and Shiraishi, Y. A pathological study of Minamata disease in Japan, Acta Neuropathol 2:40, 1962. 76. Brown, H.S. Bishop, D.R.; Rowan, C.A. The role of skin absorption as a route of exposure for volatile organic compounds in drinking water, Am J Pub Health 74: 479-484, 1984. 77. Randolph, T.G. Ecologic orientation in medicine: Comprehensive environmental control in diagnosis and therapy. Ann Allergy. 23:7-22, 1965.
OCR for page 188
Multiple Chemical Sensitivities: A Workshop 78. Randolph, T.G. The ecologic unit. Hospital Management, Pan I, 97:45, 1965; Pan II, 97:46, 1965. 79. Wilson, C.W.M. Hypersensitivity to Maine tap water in children: its clinical features and treatment. Nutrition and Health 2:51-63, 1983. 80. Juhlin. L.: Incidence of intolerance to food additives. Int J Dermatol 19(10):548-51, Dec., 1980. 81. Fries, J.H.: Food allergy: Current concerns. Ann Allergy 46(5):260-3, May, 1981. 82. Bell, I., King, D.: Psychological and physiological research relevant to clinical ecology: An overview of the recent literature. Clin Ecol, 1982. 83. Condemi, J.J.: Aspirin and food dye reactions. Bull N.Y. Acad Med 57(7):600-7, Sep., 1981. 84. Rea, W.J. Environmentally triggered small vessel vasculitis. Annals of Allergy, 38:245-51, 1977. 85. Potkin, S.G.; Weinberger, D.; Kleinman, J. et al. Wheat gluten challenge in schizophrenic patients. Amer J. Psychiat.138:1208-1211, 1981. 86. Hanninen, H.; Eskelinen, L.; Husman, K.; and Nurminen, M. Behavioral effects of long-term exposure to a mixture of organic solvents. Scald. J. Work Environ. Health. 4:240-55, 1976. 87. Randolph, T.G. The history of ecologic mental illness. In C.A. Frazier (Ed.), Annual Rev Allergy 1973. Hushing, NY: Med Exam Pub Co, 1974. 88. Savage, G.H. Insanity and Allied Neuroses Philadelphia: Lea and Febiger, 1884. 89. Rea, W.J.; Butler, J.R.; Laseter, J.L.; and DeLeon, I.R. Pesticides and brain function changes in a controlled environment. Clinical Ecology, 2(3):145-50, 1984. 90. Lindemayr, H. Schmidt, J.: Intolerance to acetylsalicylic acid and food additives in patients suffering from recurrent urticaria (author's transl.). Wien Klin Wochenschr 91(24):817-22, Dec., 21, 1979. 91. Hanington, E.: Diet and migraine. J. Hum. Nutr. 34:175-80,1980. 92. Dahl, R.: Sodium salicylate and aspirin disease. Allergy 35(2):155-6, Mar., 1980. 93. Wuthrich B., Fabro, L.: Acetylsalicylic acid and food additive intolerance in urticaria, bronchial asthma and rhinopathy. Schweiz. Med. Wochenchr. 111(39):1445-50, Sep. 26, 1981. 94. Tabuenca, J.M.: Toxic-allergic syndrome caused by ingestion of rapeseed oil
OCR for page 189
Multiple Chemical Sensitivities: A Workshop denatured with aniline. Lancet 12:2(8246):567-8, Sep. 1981. 95. Cullen M. ed. Workers with Multiple Chemical Sensitivities. Occup. Med. State of the Art Reviews. 2(4),1987. 96. Thune, P.: Photosensitivity and allergy to cosmetics. Contact Dermatitis 7(1):54-5, Jan., 1981. 97. Zaynoun, S.T., Aftimos, B.A., Tenekjian, K.K., Kurban, A.K.: Berloque dermatitis a continuing cosmetic problem. Contact Dermatitis 7(2):111-6, Mar., 1981. 98. Fisher, A.A.: Reactions to popular cosmetic humectants, Part III. Glycerin, propylene glycol, and butylene glycol. Curtis 26(3):243-4, 269, Sep., 1980. 99. Guin, J.D., Berry, V.K.: Perfume sensitivity in adult females. J Am Acad Dermatol 3(3):299-302, Sep., 1980. 100. Foussereau, J., Reuter, G., Petitjean, J.: Is hair dyed with PPD-like dyes allergenic? Contact Dermatitis 6(2):143, Jan., 1980. 101. Klein, A.D. 3d, Rodman, O.G.: Allergic contact dermatitis to paraphenylenediamine in hair dye. Milit Med 146(1):46-7, Jan., 1981. 102. Ramsay, C.A.: Skin responses to ultraviolet radiation in contact photodermatitis due to fentichlor . J Invest Dermatol 72(2):99-102, Feb., 1979. 103. Schlueter, L.E., Soto, R.J., Baretta, E.D., Herrmann, A.A., Ostrander, L.E., Stewart, R.D.: Airway response to air spray in normal subjects and subjects with hyperreactive airways. Chest 75(5):544-8, May, 1979. 104. Stoll, D., King, L.E., Jr.: Disulfiram-alcohol skin reaction to beer-containing shampoo. JAMA 244(18):2045, Nov., 1980. 105. Hindson, Phenyl salicylate (Salol) in a lip salve. Contact Dermatitis 6(3):216, Apr., 1980. 106. Fisher, A.A.: Permanent loss of finger nails from sensitization and reaction to acrylic in a preparation designed to make artificial nails. J Dermatol Surg Oncol 6(1):70-1, Jan., 1980. 107. Jordan, W.P., Jr.: Contact dermatitis from D & C yellow 11 dye in a toilet bar soap. J Am Acad Oermatol 4(5):613-4, May, 1981. 108. Larson, W.G.: Sanitary napkin dermatitis due to the perfume. Arch Dermatol 115(3):363, Mar., 1981. 109. Mathias, C.G., Chappler, R.R., Maibach, Hi: Contact urticaria from cinnamic aldehyde. Arch Dermatol 116(1):74-6, Jan., 1980.
OCR for page 190
Multiple Chemical Sensitivities: A Workshop 110. Aust, L.B., Maibach, H.I.: Incidence of human skin sensitization to isostearyl alcohol in two separate groups of panelists. Contact Dermatitis 6(4):269-71, Jun., 1980. 111. Sertoli, A., Di Fonzo, E., Spallanzani, P., Panconesi, E.: Allergic contact dermatitis from thimerosal in a soft contact lens wearer. Contact Dermatitis 6(4):292-3, Jun., 1980. 112. Zeigen, S.R., Jacobs, I.H., Weinberger, G.I.: Delayed hypersensitivity to thimerosal in contact lens solutions. J Med Soc NJ 78(5):362-4, May, 1981. 113. Jackson, R.T., Nesbitt, L.T., Jr., DeLeo, V.A.:6-Methylcoumarin photocontact dermatitis. J Am Acad Dermatol 2(2):124-7, Feb., 1980. 114. ElSaad El-Rifaie, M.: Perioral dermatitis with epithelioid cell granulomas in a woman: a possible new etiology. Acta Derm Venereal (Stockh) 60(4):359-60, 1980. 115. Burrows, D., Campbell, H.S.: Contact dermatitis to polyesters in finishes. Contact Dermatitis 6(5):362-3, Aug., 1980. 116. Imbeau, S.A., Reed, C.E.: Nylon stocking dermatitis. An unusual example. Contact Dermatitis 5(3):163-4, May, 1979. 117. McDaniel, W.H., Marks, J.G., Jr.: Contact urticaria due to sensitivity to spray starch. Arch Dermatol 115(5):628, May, 1979. 118. Larson, F.S., Brandrup, F.: Nickel release from metallic buttons in blue jeans. Contact Dermatitis 6(4):298, Jun, 1980. 119. Rudzki, E., Kozlowska, A.: Causes of chromate dermatitis in Poland . Contact Dermatitis (63):191-6, Apr., 1980. 120. Kleinhans, Days. Formaldehyde contact allergy. Derm Beruf Umwelt 28(4):101-3, 1980. 121. Klaschka, F., yon Nieding, F., Walter, R. Skin sensitization to wood preservatives containing pentachlorophenol (PGP). Zentralbl Arbeitsmed Arbeitsschutz Prophyl 29(6):150-4, Jun., 1979. 122. Bach, B., Pedersen, N.B.: Contact dermatitis from a wood preservative containing tetrachloroisophthalonitriles. Contact Dermatitis 6(2):142, Jan., 1980. 123. Spindeldreier, A., Deichmann, B.: Contact dermatitis against a wood preservative with a new fungicidal agent. Derm Beruf Umwelt 28(3):88-90, 1980. 124. Frigas, E., Filley, W.V., Reed, C.E.: Asthma induced by dust from urea-formaldehyde foam insulating material. Chest 79(6):706-7, Jun., 1981. 125. Matsushita, T., Nomura, S., Wakatsuki, T.: Epidemiology of contact dermatitis from
OCR for page 191
Multiple Chemical Sensitivities: A Workshop pesticides in Japan. Contact Dermatitis 6(4):255-9, Jun., 1980. 126. Rudzki, Mapiorkowska, Dermatitis caused by the Polish fungicide Sadoplon 75. Contact Dermatitis 6(4):300-1, Jun, 1980. 127. Weinstein, L.H., Fellner, M.J.: Rubber band dermatitis. Int J Dermatol 18(7):558, Sep., 1979. 128. Conde-Salazar, L., Romero, L., Guimaraens, D.: Metal content in Spanish coins. Contact Dermatitis 7(3):166, May, 1981. 129. Fregert, S.: Epoxy dermatitis from the nonworking environment. Br J Dermatol 105 Sppl 21:63-4, Sep., 1981. 130. Guin. J.D.: Contact dermatitis to perfume in paper products letter. J Am Acad Dermatol 4(6):733-4, June, 1981. 131. Marks, J.G., Jr.: Allergic contact dermatitis from carbonless copy paper. JAMA 245(22):2331-2. June 12, 1981. 132. Calnan, C.D.: Dermatitis from ivy (Hedera canariensis variegata). Contact Dermatitis 7(2):124-5, Mar., 1981. 133. Sugai T., Takahashi, Y., Okuno, F.: Chrysanthemum dermatitis in Japan. Contact dermatitis 6(2):155, Jan., 1981. 134. Fuchs, E. Insects as inhalant allergens. Allergol Immunopathol (Madr) 7(3):227-30, May-June, 1979. 135. Levine, S. and Kidd, P. Antioxidants Adaptations, BioDivision, Allergy Research Group, San Leando, California, 1985. 136. Theorell, H.; Blambock, M.; Kockum, C. Demonstration of reactivity to airborne and food antigen in cutaneous vasculitis by variation in fibrino 6 peptide and others, blood coagulation, fibrinolysis, and complement parameters, Thrombo Haemo Sts (Stattz), 36: 593, 1976. 137. Gaworoki, C.L. and Sharma, R.P. The effects of heavy metals on (3H) thymidine uptake ha lymphocytes, Toxicol App Pharmacol, 46(2): 305-13, 1978. 138. Winslow, S.G. The effects of environmental chemicals on the immune system: a selected bibliography with abstracts, Oak Ridge, Tennessee: Toxicology Information Response Center, Oak Ridge National Laboratory, 1981, pp. 1-36. 139. Rea, W.J. and Suits, C.W. Cardiovascular disease triggered by foods and chemicals In Gerrard, J.W. (Ed.) Food allergy: new perspectives, Springfield, Illinois: 1980. Charles C. Thomas, 1980.
OCR for page 192
Multiple Chemical Sensitivities: A Workshop 140. Jakoby, W.B. (Ed.) Enzymatic Basis of Detoxication, Vol. I 1983, Academic Press. 141. Reeves, A.L. (Ed.) Toxicology: Principles and Practice Vol. 1981, John Wiley & Sons, New York. 142. O'Shea, J.; Porter, A. Double-blind study of children with hyperkinetic syndrome treated with multi-allergen extract sublingually, J Learning Disabil 14: 189-91, 1981. 143. Forman, R.A. Critiques of evaluation studies of sublingual and intracutaneous provocation tests for food allergy, Med hypotheses 7: 1019-27, 1981. 144. Miller, J.B. A double-blind study of food extract injection therapy, Ann Allergy 38(3): 185-91, 1977. 145. Boris, Shift, Weindorf, S. Bronchoprovocation blocked by neutralization therapy, J Allergy Clin Immunol 7: 92, 1983. 146. Rea. W.J., Pan,Y, Johnson, A. R. Clearing of Toic Volatile Hydrocarbons from Humans. Clin Ecol 5(4):166-170, 1987/88. 147. Boris M., Schiff M., Weindorf S. Antigen-Induced Asthma Attenuated by Neutralization Therapy. Clin Ecol, 1985; 3:59-62. 148. Boris M., Schiff M., Weindorf S. Injection of Low-dose Antigen Attenuates the Response to Subsequent Bronchoprovocative Challenge. Otolaryngol-Head Neck Surg, 1988; 98:538-545. 149. Miller JB, Intradermal Provocative/Neutralizing Food Testing and Subcutaneous Food Extract Injection Therapy. In Brostoff J, Challacombe S, (Eds): Food allergy and Intolerance, London, Bailliere Tindall Publishers, 1987: 932-946. 150. Rea WJ, et al: Elimination of Oral Food Challenge Reaction by Injection of Food Extracts, Arch Otolaryngoll, 1984; 110:248-252. 151. Scadding G. Brostoff, J.: Low-dose Sublingual Therapy in Patient With Allergic Rhinitis Due to House Dust Mite, Clin Allergy, 1986; 16: 483-491.
Representative terms from entire chapter: