(Appeared in the Journal of Australasian College of Nutritional and Environmental Medicine Vol 23 No 1 April 2004. pages 3 – 8 by Luke Curtis MS, CIH, Allen Lieberman MD, Martha Stark MD, William Rea, Marsha Vetter MD PHD. Permission granted to be used on this website.)

Introduction

In recent years, public attention has become increasingly focused on the very real problem of mold (fungi) inside both home and workplace and on the very real dangers posed by such mold exposure to human health. This position paper is presented by the American Academy of Environmental Medicine (AAEM) to describe the current knowledge of adverse health effects of indoor mold. There is considerable evidence in the medical literature validating the many different health effects reported in airborne mold exposed patients.

Indoor airborne mold exposure frequently causes adverse human health effects with injury to and dysfunction of multiple organs and systems including:

1) respiratory

2) nervous

3) immune

4) haematological systems

5) the skin

Indoor mold is also a common cause of life-threatening systemic infections in immuno-compromised patients.

Molds are Common in the Indoor Environment

Fungi (or molds) are ubiquitous in both indoor and outdoor environments. Molds are frequently spread by airborne spores. Mold and mold spores require moisture and a food source like cellulose or decaying food to grow.1 As mold spores swell with water and grow, they elongate, forming balloon-like protuberances (hyphae) which secrete digestive enzymes and mycotoxins. The fungus then digests the food source to support its growth.

About 100,000 fungal species have already been identified; in fact fungi are estimated to comprise an astounding 25% of the world’s biomass.2 Various surveys of homes in North America and Europe have reported that visible mold and/or water damage are found in 23% to 98% of all homes.3-6 There are no official standards, at this time, for indoor airborne fungus concentrations. However, indoor fungal levels above a range of 150 to 1,000 colony-forming units per cubic meter of air (cfu/m3) are considered to be sufficient to cause human health problems.4,7-9 Numerous reports have documented that indoor air can often be contaminated with indoor fungal spore levels well in excess of 1,000 cfu/m3.10-17 The most common indoor fungi generally collected are Cladosporium, Aspergillus and Penicillium.10-17 Alternaria, Stachybotrys, Rhizopus, Mucor, Wallemia, Trichoderma, yeasts, Botrytis, Epicoccum and Fusarium species are often being found indoors as well.10- 17

Foreclosures, lawsuits and insurance claims due to mold problems are common. Policyholders of America report receiving about 50 calls a week about homes with mold problems undergoing foreclosure.18 In 2002, an estimated 10,000 mold related cases were pending in US courts.19 In 2002, the insurance industry paid out $2 billion in mold related claims in Texas alone.20

Mold Related Health Symptoms are Common and Varied

Many patients have been reporting multiple ill health effects from their exposures to mold. Studies of more than 1,600 patients suffering ill effects from fungus exposure were presented at one meeting in Dallas in 2003 (21st Annual Symposium of Man and His Environment in Dallas, Texas, June 200319- 22).21-25

To cite a few studies: Lieberman21 examined 48 mold-exposed patients who had the following health problems:

1. muscle and/or joint pain 71%

2. fatigue/weakness 70%

3. neurocognitive dysfunction 67%

4. sinusitis 65%

5. headache 65%

6. gastrointestinal problems 58%

7. shortness of breath 54%

8. anxiety/ depression/ irritability 54%

9. vision problems 42%

10. chest tightness 42%

11. insomnia 40%

12. dizziness 38%

13. numbness/ tingling 35%

14. laryngitis 35%

15. nausea 33%

16. skin rashes 27%

17. tremors 25%, and

18. heart palpitations 21%.

Rea’s23 study of 150 indoor mold-exposed patients found the following health problems:

1. fatigue 100%

2. rhinitis 65%

3. memory loss and other neuropsychiatric problems 46%

4. respiratory problems 40%

5. fibromyalgia 29%

6. irritable bowel syndrome 25%

7. vasculitis 4.7%, and

8. angio-oedema 4.0%.

These clinical reports demonstrate the multi-system adverse effects of airborne mold. There is now considerable evidence in the medical literature that indoor airborne fungi exposure can cause numerous adverse health effects in multi-organ systems.

Mechanisms of Mold-Related Health Effects

Fungi can exert ill health effects by 3 mechanisms:

1) infection

2) allergy

3) toxicity.

Serious infections by such fungi as Candida, Aspergillus and Pneumocystis are common and mostly involve severely immunocompromised patients.26-28 Fungi such as Candida, Histoplasmosis, Cryptococcus, Blastomyces and Coccidioides can infect internally immunocompetent people.29 Fungi such as Trichophyton, Candida and Malasezia commonly cause minor skin infections in immunocompetent humans.28

At least 70 allergens have been well characterized from spores, vegetative parts and small particles from fungi (0.3 microns and smaller).30,31 Allergies to fungal allergens are very common, with a review of 17 studies finding that 6% to 10% of the general population and 15% to 50% of atopics had immediate skin sensitivity to fungi32.

Fungi produce a wide variety of toxic chemicals called mycotoxins.1,33,34 Some common mycotoxins include:

1. Aflatoxins – very potent carcinogens and hepatotoxins produced by some Aspergillus species;

2. Ochratoxins – nephrotoxic and carcinogenic – produced by some Aspergillus and Penicillium;

3. Sterigmatocystin – immunosuppressive and a liver carcinogen produced by Aspergillus species especially A. versicolour; and

4. Trichothecenes are produced primarily by Stachybotrys and Fusarium species, and have been reported to inhibit protein synthesis, cause haemorrhage and vomiting.

Fungi also produce beta glucans which have immunological effects.35 The smell of molds come primarily from volatile organic compounds.36

Adverse human and animal effects from mycotoxin-contaminated foodstuffs have been well recognized since the early 20th century.33,37 But the pathway of mycotoxin injury through inhalation is questioned.38 In the absence of ethical, controlled studies on human inhaled mycotoxin exposure, only animal controlled exposure and human epidemiology studies can be used. The literature demonstrates that significant amounts of mycotoxins (including ochratoxin, sterigmatocystin and trichothecenes) are present in indoor dust39-43 and in fungal spores which can be absorbed through the respiratory route.34,37,44,45 Patients exposed to indoor Stachybotrys have been found to have measurable blood levels of the Stachybotrys haemorrhagic toxin stachylysin.46 Levels of trichothecene mycotoxins in the urine have also been found in significantly higher levels in patients exposed to high indoor fungus levels, as opposed to a control group not exposed to high indoor fungus levels.47 Blood ochratoxin levels have been found to be significantly higher in food industry workers exposed to airborne ochratoxin versus unexposed controls.43 These findings clearly demonstrate an inhaled pathway for entry into the body.

Sampling for Mold Exposure

Indoor fungus sampling is most commonly performed by measuring airborne levels of viable (culturable) or total (viable and non viable) spores.48,49 Some of the airborne viable sampling methods, such as Andersen samplers, collect air for only a few minutes.

Settle plates are an inexpensive method to get a semi-quantitative measure of indoor airborne fungus levels. Viable and non viable airborne spore counts can vary considerably over a period of minutes, so air sampling over several periods of time may be necessary to accurately characterize airborne fungal spore levels.48,49

However, airborne fungus measurements fail to take into consideration non-airborne mold contamination such as mold contamination in dust or surfaces (often visible to the naked eye) and mycotoxins in air, dust and on surfaces.48,50 Therefore testing the settled dust for fungi and mycotoxins is often recommended.48,49 In order to secure a more complete assessment, therefore, it is often recommended that airborne measurements be supplemented by testing for molds and mycotoxins in already-settled dust or air.48,49

Other techniques such as PCR (Polymerase Chain reaction), ELISA (Enzyme Linked Immunosorbent Assay), and measurement of fungal volatile organic chemicals, polysaccharides, ergosterol and beta glucans can also be useful in assaying indoor environments for molds and their allergens and mycotoxins.48

For a helpful overview of sampling methods, please see Pasanen48 and Macher.51 For an informative guide to the classification, identification and biology of common indoor fungi, see Samson.1 Several good guides exist for prevention and remediation of indoor fungi problems.51-53

Indoor Mold Exposure and Respiratory Problems

Many epidemiological studies have noted that residential exposure to molds and/or chronic dampness can increase asthma/wheezing incidence or morbidity in both children and adults.4-6,54-67 Asthma and related conditions are very common in the USA, with an overall incidence of about 5.4% among all age groups and incidences as high as 27% in inner city children.68 Studies with infants have reported that higher fungal exposures are associated with more wheezing, coughing and respiratory illness.69,70 Higher indoor beta glucan levels have been associated with significantly higher levels of chest tightness and joint pain71 Non-industrial occupational mold exposure has been reported to be associated with significantly higher levels of asthma, sinusitis, irritated skin and eyes and chronic fatigue.72-6

One study found that patients exposed to high indoor fungus levels had significantly lower lung function than unexposed controls.24 Higher outdoor fungal concentrations have been linked to higher asthma death rates77 and high asthma incidence78,79 in children or young adults. Challenge exposures with Penicillium and Alternaria extracts equivalent to high outdoor levels of fungus were noted to severely lower lung function in asthmatics.80 Skin sensitivity to Alternaria has been linked to much higher risk of respiratory arrest.81 Various epidemiological studies have linked skin sensitivity to common indoor fungi and higher asthma incidence or severity82-86 and higher rates of sinusitis.87

Airborne fungal exposure causes sinusitis, bronchopulmonary aspergillosis and hypersensitivity pneumonitis.88-89 An estimated 14% of the USA population suffer from rhinosinusitis and related conditions.90

Allergic fungal sinusitis was diagnosed on the basis of fungal growth in nasal secretions and presence of allergic mucin in 93% of 101 consecutive patients undergoing sinus surgery.90 Another study was able to recover and culture fungi from the sinuses of 56% of 45 patients undergoing endoscopic sinus surgery for chronic rhinosinusitis.91 A longterm cohort study of 639 patients with allergic fungal sinusitis demonstrated that remedial steps taken to reduce fungal exposure (by utilizing, for example, air filters, ionizers, moisture control and anti-microbial nasal sprays) significantly reduced rhinosinusitis and improved nasal mucosa morphology.22 This study concluded that failure to reduce airborne fungus levels to less than 4 per hour on a settle plate failed to resolve the sinusitis.22

Although, historically, anti-fungal drugs have generally not been recommended for treatment of fungal sinusitis,88,89 recent studies have found beneficial effects of oral and nasal medication for sinusitis patients.22,92 Several studies have linked residential exposure to fungi with hypersensitivity pneumonitis.93-95

Stachybotrys and Haemorrhagic Effects

fungus levels, as opposed to a control group
not exposed to high indoor fungus levels.47
Blood ochratoxin levels have been found to
be significantly higher in food industry
workers exposed to airborne ochratoxin versus
unexposed controls.43 These findings clearly
demonstrate an inhaled pathway for entry into
the body.

Exposure to high indoor levels of Stachybotrys, Aspergillus and other fungi has been epidemiologically associated with infant lung haemorrhage.96-100 Although questions were raised after this association was discovered,101 it meets many epidemiologic criteria for causality.102 Acute infant pulmonary haemorrhage can be rapidly fatal; when the infant survives, lung blood vessel damage is present and deposits of haemosiderin will remain in the lung macrophages and can be seen in tissue obtained during bronchoscopy.97

Stachybotrys fungi produce a wide range of trichothecene mycotoxins (including satratoxins), several roridin epimers, verrucarin J and B and hemolysin.34,99 A haemorrhagic protein called stachylysin has been isolated from Stachybotrys collected from homes of infants with lung haemorrhage,103,104 and from serum of patients with residential Stachybotrys exposure.46 It is hypothesized that infants, with their rapidly growing lungs, are more susceptible to the toxic effects of Stachybotrys mycotoxins.105 Studies with Stachybotrys-exposed adults have noted a significantly higher incidence of health problems such as lower airway problems, wheezing, skin and eye irritation, flu-like symptoms and chronic fatigue.106 Stachybotrys has been isolated from the lungs of a child with pulmonary haemosiderosis.107

Immunological Changes

Fungal exposure can alter immunological parameters. Some studies have reported that indoor fungus-exposed patients have higher serum levels of IgG, IgA and IgM antibodies to common fungi, trichothecenes and satratoxins.108-110 IgG antibodies to 9 common indoor fungi were significantly higher in subjects with sinusitis, versus non sinusitis subjects in a moldy school.111 Other studies note no significant increases in fungal IgG112,113 or fungal IgE108 in fungus-exposed patients.

Indoor fungal exposure has been associated with altered levels of T4, T8 and NK cells and higher levels of auto-antibodies.23,114,115 Indoor glucan exposure has been associated with a lower proportion of cytotoxic T-cells (CD8+SF61+) and with secretion of tumour necrosis factor higher than from homes with lower levels of beta glucans.116

Studies of animals orally given such common mycotoxins as aflatoxins, ochratoxins and trichothecenes show considerable immune impairment, including depression of T cell, B cell and macrophage immunities.117 Human cell line studies have also found that many mycotoxins can suppress T cell, B cell and NK activity at serum concentrations similar to those found in indoor mold exposed patients.118 Thus, airborne exposure to mycotoxin is seen to cause harmful effects to the immune system.

Neurological Dysfunction

Indoor airborne mold exposure causes neurologic dysfunction and cognitive deficits. Clinical reports on large numbers of mold exposed patients found significant fatigue and weakness in 70% to 100% of cases, and neurocognitive dysfunction, including memory loss, irritability, anxiety and depression, in over 40% of the patients.21,23 Numbness, tingling and tremor were also found in a significant number of patients.21,23 These signs and symptoms constitute classic manifestations of neurotoxicity.119

A study of 43 mold-exposed patients found they performed significantly more poorly than 202 controls on many neuropsychiatric tests including balance sway speed, blinking reflex, colour perception, reaction times and left grip strength (P<0.0001 in each case).120

Quantitative electro-encephalogram studies have also noted significant longer nerve latencies in fungus-exposed patients.120 A triple-headed SPECT brain scan revealed neurotoxic patterns in 26 of 30 (87%) moldexposed patients.121

An iriscorder study of autonomic nervous function in 60 mold-exposed patients found 95% had abnormal autonomic responses of the pupil.23 Visual contrast sensitivity studies were often abnormal in indoor mold-exposed patients.23

Additional studies have reported that mold exposed patients do significantly more poorly on tests of attention, balance, reaction time, verbal recall, concentration, memory, finger tapping.24, 122-124 Most of these patients also experienced many health problems including chronic fatigue, headaches, insomnia and decreased balance, concentration and attention.

Studies of 10 indoor-mold-exposed children and 378 indoor-mold-exposed adults found significantly more neurophysiological abnormalities than in controls; this included abnormal EEGs and abnormal brainstem, visual and somatosensory evoked potentials as compared to 10 control children.25,125

The large number of objective neuropsychological findings in symptomatic patients support the findings that exposure to indoor molds can have adverse health effects.

Renal Dysfunction

Exposure to fungi may also cause kidney dysfunction. It is well know that ochratoxin contaminated-food is nephrotoxic.126,127 Indoor exposure to ochratoxin may also be nephrotoxic. A study was presented of a family who presented with increasing thirst and urination, lethargy, and skin rash. Considerable amounts of ochratoxin were found in the house dust. The family recovered after moving to another home.38

Life Threatening Fungal Infections in the Immuno-compromised

In recent years, the incidence of life threatening infections in immuno-compromised patients from Aspergillus and other common fungi has been growing rapidly.128,129 Invasive aspergillosis is very common among immuno-compromised patients with reported incidence rates in the following patients: lung transplants 17-26%; allogenic bone marrow transplants 5-15%; acute leukaemia 5-24%; and heart transplant 2-13%.130,131 Even with strong anti-fungal drugs and intense hospital treatment, mortality rates from invasive aspergillosis range from 50% to 99% in the immunocompromised. 132,133

Environmental control plays a key role in preventing Aspergillus infections. Several studies have linked hospital construction work to increased rates of invasive aspergillosis.134-7 Environmental controls such as using HEPA filters, sealing rooms, regular cleaning of rooms, and using anti-fungal copper-8-quionolate paint have been shown to both significantly reduce airborne levels of Aspergillus and to significantly reduce rates of invasive aspergillosis in immuno-compromised hospital patients.135-141 Other recent research has indicated that a large number of Aspergillus spores can spread through water supplies142 and that cleaning shower facilities can significantly lower airborne levels of Aspergillus.143

Diagnosis and Treatment of Mold Related Health Problems

A careful environmental and medical history is an essential first step in evaluating a patient for mold-related health problems.52,144-6 Particular attention should be paid to any history of exposure to visible mold and/or water damage at the home or workplace. Environmental sampling for viable spores, total spores, and mycotoxins in the air and dust can provide important exposure information. For patients suspected of having substantial fungal exposure, a battery of sophisticated laboratory tests have been developed to:

1. test for antibodies to molds and mycotoxins in the sera of these patients,108,109

2. other immunological tests,115

3. urine and blood testing for mycotoxins,47

4. a basic metabolic panel to test for several important parameters (including electrolytes, blood sugar and kidney status).

Visual contrast sensitivity tests should be done on all mold-exposed patients. The use of standard neuropsychological tests batteries23,122-4 as well as autonomic nerve testing, EEG and brain imaging techniques like SPECT and MRI can be very helpful tools in documenting mold-related neurological damage.25,120,121,125,144 Use of pulmonary function tests is also useful for patients with respiratory symptoms.24,120

If patient symptoms or a review of systems suggests involvement of ears, nose throat, gastrointestinal system, the eyes or the heart, then consultation with physicians knowledgeable about environmental exposures (be the doctor an ENT specialist, a gastroenterologist, and ophthalmologist or a cardiologist) may be very useful. Failure to perform objective evaluations for accessing system or organ dysfunction account for the presently accepted position that airborne mold exposures have no significant adverse health effects.38

Other common indoor environmental exposures should also be considered as a potential source of health problems.

Common non-fungal indoor environ-mental factors include poor ventilation, carbon monoxide from faulty heat sources, pesticides, second hand tobacco smoke, petrochemicals such as cleaners/building materials/solvents, formaldehyde from outgassing carpets and building materials, bacteria, and allergens from the fur, feathers and saliva of common household animals like cockroaches, dust mites, cats, dogs, caged birds, and pigeons. Exposure to ozone, second-hand tobacco smoke, formaldehyde, cockroach allergen and viral infections can also have a synergistic effect with fungal exposure, to worsen asthma and rhinitis.147-151

The most important part of treatment for mold-exposed patients is avoidance of fungal exposure and remediation of mold contamination in the home and workplace. Any water leaks, and flooded or damp areas should be rectified immediately. Non-porous surfaces like floors and walls which have visible mold growth should be cleaned. Porous waterlogged materials like carpet and furniture should be thrown out. Control of humidity is important to control mold growth.

The use of air conditioners and dehumidifiers can significantly reduce summertime indoor airborne mold concentrations.10,152 HEPA air filters can also significantly reduce indoor airborne fungus concentrations.141 For cleanup of severe indoor water or mold problems, use of protective equipment like face masks and/or use of a professional remediation firm may be essential.50-2

Some studies with laboratory animals suggest that a high quality diet with adequate anti-oxidant vitamins, selenium, phytochemicals, methionine and total protein, can reduce the harmful effects of food mycotoxins.

Use of sublingual or injective fungal immunotherapy has been shown to be beneficial to some patients sensitized to common indoor molds such as Alternaria and Cladosporium herbarium.153,154 Other therapies found helpful include:

1. detoxification (sauna, massage, exercise)

2. correction of identified immune deficiencies

3. use of topical, nasal or oral anti-fungal drugs when indicated. Some studies with laboratory animals suggest that a high quality diet with adequate anti-oxidant vitamins, selenium, phytochemicals, methionine and total protein can reduce the harmful effects of food mycotoxins.155, 156

Summary

Indoor airborne mold and/or mycotoxin exposures cause many multisystem adverse human health effects, as indicated by the more than 100 references cited. Healthcare professionals, building managers, home owners and the general public need to be much more aware of their potential adverse health effects, the need for proper building remediation and the need for appropriate patient diagnosis and treatment. There is sufficient data from the medical literature and the large number of clinical reports to substantiate the reported adverse health effects of indoor airborne mold. Indoor mold and mycotoxin exposure absorbed through the respiratory route can be a major pathway of injury by all 3 mechanisms: infection, allergy, and toxicity.

References

1. Samson R et al. Introduction to Food and Airborne Fungi. Centraalbureau voor Schimmelcultures, PO Box 85167, 3508 AD UTRECHT, The Netherlands 2000.

2. Miller JD. “Fungi as contaminants of indoor air.” Atmospheric Environment 1992 26A (12):2162-2172.

3. Presternon DR. “Perceived moisture problems in Iowa Homes.” Technical Note, Forest Products Journal 1991;41(6):47-48.

4. Platt S et al. “Damp housing, mold growth & symptomatic health state.” BMJ June 24, 1989; 298:1673-8.

5. Brunekreef B et al. “Home dampness and respiratory morbidity in children.” American Rev. of Resp. Disease 1989;140:1363-1367.

6. Dales R et al. “Respiratory Health Effects of home dampness and molds among Canadian Children.” American J of Epidemiol. 1991a;134(2):196-203.

7. Etzel R. Indoor air pollutants in homes and schools. Pediatric Clinics of North America October 2001;48(5):1153-65.

8. Flannigan B et al. “Allergic and toxigenic microorganisms in houses.” J of Applied Bacteriol. 1991;70:61S-73S.

9. Dhillion M. “Current status of mold immunotherapy.” Annals of Allergy 1991;66:385.

10. Curtis L et al. “Bioaerosol concentrations in the Quad Cities 1 year after the 1993 Mississippi River floods.” Indoor & Built Environment 2000;9:35-43.

11. Shelton B et al. “Profiles of airborne fungi in buildings and outdoor environments in the United States.” Applied & Environmental Microbiol. April 2002;68(4):1743-1753.

12. Ren P et al. “Comparisons of seasonal fungal prevalence in indoor and outdoor air and in house dwellings in one Northeast American county.” J of Exposure Analysis & Environmental Epidemiol. 1999;9:560-568.

13. Pei-Chih W et al. “Characteristics of indoor and outdoor airborne fungi at suburban and urban homes in two seasons.” Science of the Total Environment 2000;253:111-8.

14. Li CS et al. “Characteristics of airborne microfungi in subtropical homes.” Science of the total environment. October 28, 1994;155(3):267-271.

15. Ebner E et al. “Indoor and outdoor incidence of airborne fungal allergens at low and high alpine environments.” Mycology Research 1992;97:117-124.

16. Solomon WR. “A volumetric study of winter fungus prevalence in the air of midwestern homes.” J of Allergy and Clinical Immunol. January 1976;57(1):46- 55.

17. Beaumont F et al. “A volumetric-aerobiological study of seasonal fungus prevalence inside and outside dwellings of asthmatic patients living in northeast Netherlands.” Annals of Allergy December 1984;53(6):486-492.

18. Hevesi D. “Harmful or not, mold grows as a costly problem.” Chicago Tribune page 7E, March 30, 2003.

19. Umberger M. “The Start that upstaged the economy.” Chicago Tribune, January 13, 2002 at 1- available at WL 2612028, database ALLNEWS.

20. (No Author) “Mold Claims Hit $4 billion in Texas.” Insurance Journal, May 27, 2003, http://insurancejournal.com

21. Lieberman A. “Explosion of mold cases in homes, workplaces and occupational medicine practices.” Presented at the 21st Annual Symposium on Man and His Environment in Health and Disease, Dallas, Texas. June 19-22, 2003

22. Dennis D. “Guidelines and Theory for Treatment of chronic fungal sinusitis with reduction of environmental air mold load and anti-microbial nasal sprays based on 14 years clinical experience in 639 patients.” Presented at the 21st Annual Symposium on Man and His Environment in Health and Disease, Dallas, Texas. June 19-22, 2003

23. Rea W. “Diagnosis of Mold and Mycotoxin Sensitivity.” Presented at the 21st Annual Symposium on Man and His Environment in Health and Disease, Dallas, Texas. June 19-22, 2003

24. Kilburn K. “How molds and mycotoxins affect human brains.” Presented at the 21st Annual Symposium on Man and His Environment in Health & Disease, Dallas, Texas. June 19-22, 2003

25. Campbell A, High W, Anyawu E. “Immunological and Neurophysiological Abnormalities in Adults with Exposure to Molds.” Presented at the 21st Annual Symposium on Man and His Environment in Health & Disease, Dallas, Texas. June 19-22, 2003 (Include Archives of Environmental Health paper if available).

26. Garber G. “An Overview of fungal infections.” Drugs 2001;61 Supplement 1:1-12.

27. Nicod L et al. “Fungal infections in transplant recipients.” Eur. Resp. J. January 2001;17(1):133-140.

28. Tierney L et al. Current Medical Diagnosis and Treatment. 2003 Lange Medical Books, New York City

29. Johnson P et al. “Community Acquired Fungal Pneumonias.” Seminar in Respiratory Infections March 1989;4(1):56-63.

30. Kurup V et al. “Immunobiology of fungal allergens.” Int. Arch. of Allergy & Immunol. 2002;129:181-188.

31. Gorny RL et al. “Fungal fragments as indoor air contaminants.” Applied & Environmental Microbiol. 2002;68:3522-3531.

32. Clearing the Air; Asthma and Indoor Air Exposures. Institute of Medicine, National Academy Press, 2000 Washington, DC.

33. Etzel R. “Mycotoxins.” JAMA January 23/30, 2002,287(4):425-427.

34. Nielsen KF. “Mycotoxin production by indoor molds.” Fungal Genetics & Biol. 2003;39:103-117.

35. Rylander R. “Indoor air-related effects and airborne (1>3)-beta-D-glucan.” Environmental Health Perspectives June 1999;107 Supplement 3:501-3

36. Wilkins K et al. “Volatile metabolites from mold growth on building materials and synthetic media.” Chemosphere August 2000; 41(3):437-446.

37. Bennett J et al. “Mycotoxins.” Clinical Microbiol. Reviews July 2003;16(3):497-516.

38. Hardin B et al. ACOEM Evidence Base Statement. “Adverse Health effects associated with molds in the indoor environment.” J. of Occup. & Environ. Med. May 2003;45(5):470-8.

39. Richard J et al. “The occurrence of ochratoxin A in dust collected from a problem household.” Mycopathologica 1999;146(2):99-103.

40. Smoragiewicz W et al. “Trichothecene mycotoxins in the dust of ventilation systems in office buildings.”

117. Int. Arch. of Occup. & Environ. Health 1993;65(2):113-

41. Engelhart S et al. “Occurrence of toxigenic Aspergillus versicolor isolates and sterigmatocystin in carpet dust from damp indoor environments.” Applied Environ. Microbiol. August 2002;68(8):3886-3890.

42. Johanning E. 2002 Unpublished data.

43. Iavacoli I et al. “External and internal dose in subjects occupationally exposed to ochratoxin A.” Int. Arch. of Occup. & Environ. Health August 2002;75(6):381-6. Some studies with laboratory animals suggest that a highquality diet with adequate anti-oxidant vitamins, selenium, phytochemicals, methionine and total protein, can reduce the harmful effects of food mycotoxins. Reprinted from Journal of Australasian College of Nutritional & Environmental Medicine – Vol. 23 No. 1 April 2004 5 © 2004 ACNEM & Luke Curtis et al.

44. Fischer G et al. “Relevance of airborne fungi and their secondary metabolites for environmental, occupational and indoor hygiene.” Arch. of Microbiol. 2003;179:75-82.

45. Sorenson WG. “Fungal Spores: Hazardous to Health?” Environ. Health Perspectives June 1999;107(Supplement 3):469-472.

46. Van Emon J et al. “ELISA measurement of Stachylysin in serum to quantify human exposures to the indoor mold Stachybotrys charatarum.” J. of Occup. & Environ. Med. June 2003;45:582-591.

47. Croft W et al. “Clinical confirmation of trichothecene mycotoxicosis in patient urine.” J. of Environ. Biol. 2002;23(3):301-320.

48. Pasanen AL. “A review: Fungal Exposure Assessment in Indoor Environments.” Indoor Air 2001;11:87-98.

49. Dillon HK et al. “Review of methods applicable to the assessment of mold exposure in children.” Environ. Health Perspectives June 1999; 107(Supplement 3):473-480.

50. Tiffany J et al. “Detection of Stachybotrys charatarum: the effectiveness of culturable-air sampling and other methods.” Environmental Health May 2000, 9-11.

51. Macher J editor. Bioaerosols: Assessment and Control. American Conference of Governmental and Industrial Hygienists (ACGIH) Cincinnati, Ohio 1999.

52. Eggleston PA. “Environmental Control for fungal allergen exposure.” Current Allergy & Asthma Reports September 2003;3(5):424-9.

53. Institute of Medicine Committee on the Health “Effects of Indoor Allergens: Engineering Control Strategies.” “Allergens: Assessing and Controlling Adverse Health Effects.” Engineering Control Strategies 1993;206-232 Published by National Academy Press, Washington DC.

54. Gent J et al. “Levels of household mold associated with respiratory symptoms in the first year of life in a cohort at risk for asthma.” Environmental Health Perspectives December 2002;110(12):A781-A786.

55. Dales R et al. “Adverse health effects among adults exposures to home dampness and molds.” Am. Rev. of Resp. Disease 1991b;143:505-509.

56. Ostro B et al. “Air pollution and exacerbation of asthma in African-American children in Los Angeles.” Epidemiology December 2001; 12:200-208.

57. Zock J et al. “Housing characteristics, reported mold exposure, and asthma in the European Community Respiratory Health Survey.” J. of Allergy & Clin. Immunol. August 2002;110(2):285-292.

58. Williamson I et al. “Damp housing and asthma: a case control study.” Thorax 1997;52:229-234.

59. Verhoeff et al. “Damp housing and household respiratory symptoms: the role of sensitization to dust mites and molds.” Am. J. of Epidemiol. 1995;141:103-110.

60. Strachan DP et al. “Quantification of airborne molds in the homes of children with and without wheeze.” Thorax 1990:45:382-387.

61. Brunekreef, B. “Damp housing and adult respiratory symptoms.” Allergy 1992;47: 498-502

62. Waegemaekers M et al. “Respiratory symptoms in damp homes. A pilot study.” Allergy 1989;44:192-198.

63. Jedrychowski W et al. “Separate and combined effects of the indoor and outdoor air quality on chronic respiratory symptoms adjusted for allergy among preadolescent children.” Int. J. of Occup. Med. & Environ. Health 1998; 11:19-35

64. Hu FB et al. “An epidemiological study of asthma prevalence and related factors among young adults.” J. of Asthma 1997;34(1):67-76.

65. Jaakkola J et al. “Home dampness and molds as determinants of respiratory symptoms and asthma in pre-school children.” J. of Exposure Analysis &

Environ. Epidemiol. 1993;3 (supplement 1):126-142 66. Slezak J et al. “Asthma prevalence and risk factors in selected Head Start sites in Chicago.” J. of Asthma 1998; 35(2): 203-212.

67. Lee YL et al. “Indoor and outdoor environmental exposures, parental atopy and physician diagnosed asthma in Taiwanese schoolchildren.” Pediatrics November 2003;112(5):e389-e395.

68. Sly RM. “Changing prevalence of allergic rhinitis and asthma.” Ann. of Allergy, Asthma & Immunol. March 1999;82(3):233-248.

69. Belanger K et al. “Symptoms of wheeze and persistent cough in the first year of life: associations with indoor allergens, air contaminants, and maternal history of asthma.” Am. J. of Epidemiol. August 1, 2003; 158:195-202.

70. Stark PC et al. “Fungal levels in the home and lower respiratory tract illness in the first year of life.” Am. J. of Resp. & Critical Care Med. July 15, 2003;168(2):232-237.

71. Thorn J et al. “Airways inflammation and glucan in a rowhouse area.” Am. J. of Resp. & Critical Care Med. 1998;157:1798-1803.

72. Chao HJ et al. “The work environment and workers’ health in 4 large office buildings.” Environ. Health Persp. July 2003;111(9):1242-8.

73. Pirhonen I et al. “Home dampness, molds and their influence on respiratory infections in Finland.” European Respiratory Journal 1996;9:2618-2622.

74. Koskinen OM, Husman TM, Meklin TM. “The relationship between mold and moisture observations in houses and state of health of their occupants.” Eur. Resp. J. 1999;14:1363-7.

75. Ruotsalainen R et al. “Dampness and molds in daycare centers as an occupational health care problem.” Int. Arch. of Occup. & Environ. Health 1995;66:369-374.

76. Wan GH et al. “Dampness and airway inflammation and systemic conditions in office building workers.” Arch. of Environ. Health 1999;54:58-63.

77. Targonski P et al. “Effect of environmental molds on risk of death from asthma during the pollen season.” J. of Allergy & Clin. Immunol. May 1995;95(5 Part 1):955-961.

78. Neas LM et al. “Fungus spores, air pollutants, and other determinants of peak expiratory flow rates in children.” Am. J. of Epidemiol. 1996;143(8):797-807.

79. Delfino RJ et al. “The effect of outdoor fungal spores concentrations on daily asthma severity.” Environ. Health Persp. 1997;105(6):622-635.

80. Liccorish K et al. “Role of Alternaria and Penicillium spores in the pathogenesis of asthma.” J. of Allergy & Clin. Immunol. December 1985 76(6):819-825.

81. O’Halloran M et al. “Exposure to an aeroallergen as a possible precipitating factor in respiratory arrest in young patients with asthma.” NEJM February 1991;324(6):359-363.

82. Zureik M et al. “Sensitization to airborne molds and severity of asthma: cross sectional study from European Community Respiratory Health Survey.” BMJ August 24, 2002;325(7361): 411-4.

83. Gergen PJ et al. “The association of individual allergen reactivity with respiratory disease in a national sample: data from the second National Health and Nutrition Examination Survey, 1976-1980 (NHANES II).” J. of Allergy & Clin. Immunol. 1992;90(4 Pt 1):579-588.

84. Tariq SM et al. “Sensitization to Alternaria and Cladosporium by the age of 4 years.” Clin. & Exper. Allergy 1996;26(7):794-798.

85. Perzanowski MS et al. “Association of sensitization to Alternaria allergens with asthma among school aged children.” J. of Allergy & Clin. Immunol. 1998;101(5):626-632.

86. Nelson RP et al. “Allergen specific IgE levels and mite allergen exposure in children with acute asthma first seen in an emergency department and in nonasthmatic control subjects.” J. of Allergy & Clin. Immunol. 1996; 98(2):382-388.

87. Lander F et al. “Serum IgE specific to indoor molds, measured by basophil histamine release, is associated with building-related symptoms in damp buildings.” Inflamm. Res. 2001;50:227-231.

88. Schubert M. “Medical treatment of allergic fungal sinusitis.” Annals of Allergy, Asthma & Immunol. August 2000;85(2):90-101.

89. Greenberger P. “Allergic bronchopulmonary aspergillosis, allergic fungal sinusitis and hypersensitivity pneumonitis.” Clinical Allergy & Immunol. 2002;16:449-468.

90. Ponikau JU et al. “The diagnosis and incidence of allergic fungal sinusitis.” Mayo Clinic Proceedings 1999;74:877-884.

91. Lebowitz R et al. “Isolation of fungi by standard laboratory methods in patients with chronic rhinosinusitis.” The Laryngoscope 2002; 112(12):2189-2191.

92. Rains BM et al. “Treatment of allergic fungal sinusitis with high-dose itraconazole.” American J. of Rhinology January-February 2003;17(1):1-8.

93. Apostolakos M et al. “Hypersensitivity pneumonitis from ordinary residential exposures.” Environ. Health Persp. September 2001;109(9):979-981.

94. Kita T et al. “A case of hypersensitivity pneumonitis caused by Humicola fuscoatra.” Respirology 2003;8:95-98.

95. Ando M et al. “Specific bronchoalveolar lavage IgA antibody in patients with summer type hypersensitivity pneumonitis induced by Trichosporon cutaneum.” Annual Review of Resp. Disease 1986;134:177-9.

96. Centers for Disease Control (CDC): Pulmonary Hemorrhage/ Hemosiderosis Among Infants-Cleveland, Ohio, 1993-6. MMWR 1997;46:33-35

97. Montana E et al. “Environmental Risk factors associated with pediatric idiopathic pulmonary hemorrhage and hemosiderosis in a Cleveland community.” Pediatrics 1997;99:117-124.

98. Etzel R et al. “Acute pulmonary hemorrhage in infants associated with exposure to Stachybotrys atra and other fungi.” Arch. of Pediatric & Adolescent Medicine 1998;152:757-762.

99. Vesper S et al. “Hemolysis, toxicity and randomly amplified polymorphic DNA analysis of Stachybotrys chartarum strains.” Applied & Environ. Microbiol. July 1999;65(7):3175-3181.

100. Dearborn D et al. “Clinical profile of 30 infants with acute pulmonary hemorrhage in Cleveland.” Pediatrics September 2002;110(3):627-637.

101. Center for Disease Control and Prevention CDC. Update: pulmonary hemorrhage/ hemosiderosis among infants- Cleveland, Ohio 1993-6. MMWR 2000;49:18-184.

102. Etzel T. “Stachybotrys.” Current Opinion in Pediatrics February 2003;15(1):103-6.

103. Vesper S et al. “Initial characterization of the hemolysin stachylysin from Stachybotrys chartarum.” Infection & Immunity February 2001;69(2):912-6.

104. Vesper S et al. Stachylysin may be a cause of hemorrhaging in humans exposed to Stachybotrys chartarum.” Infection & Immunity April 2002; 70(4):2065-2069.

105. Yike I et al. “Highly sensitive protein translation assay for trichothecene toxicity in airborne particulates: comparison with cytotoxicity assays.” Applied & Environ. Microbiol. January 1999;65(1):88-94.

106. Johanning E et al. “Health and immunology study following exposure to toxigenic fungi (Stachybotrys chartarum) in a water-damaged office environment.” Int. Arch. of Environ. Health 1996;68:207-218.

107. Elidemir O et al. “Isolation of Stachybotrys from the lung of a child with pulmonary hemosiderosis.”Pediatrics October 1999;104(4Part1):964-966.

108. Vojdani A et al. 2003b. “Antibodies against molds and mycotoxins after exposure to toxigenic fungi in a water-damaged environment.” Arch. of Environ. Health

(In press)

109. Vojdani A et al. 2003c. “Antibodies to molds and satratoxin individuals in a water-damaged building.” Arch. of Environ. Health (In press)

110. Savilahti R et al. “Immunoglobulin G antibodies of children exposed to microorganisms in a water-damaged school.” Pediatric Allergy & Immunol. December 2002;13(6):438-442.

111. Patovirta RL et al. “Mold specific IgG antibodies connected with sinusitis in teachers of a mold damaged school: A 2 year follow up study.” Int. J. of Occup. Med. & Environ. Health 2003;16(3):221-230.

112. Taskinen TM et al. “Immunoglobulin G antibodies to molds in school-children from moisture problem schools.” Allergy January 2002;57(1):9-16.

113. Malkin R et al. “The relationship between symptoms and IgG and IgE antibodies in an office environment.” Environ. Research February 1998;76(2):85-93.

114. Dales R et al. “Incidence of residential fungal contamination on peripheral blood lymphocyte populations in children.” Arch. of Environ. Health May/June 1998;53(3):190-195.

115. Vojdani A. 2003a “Health effects and immunotoxicology of toxigenic molds and mycotoxins.” Presented June 20, 2003 at the 21st international symposium of man and his environment in health and disease. Dallas, Texas.

6 Reprinted from Journal of Australasian College of Nutritional & Environmental Medicine – Vol. 23 No. 1 April 2004 © 2004 ACNEM & Luke Curtis et al.

116. Beijer L et al. “Mold exposure at home relates to inflammatory markers in blood.” Eur. Resp. J. February 2003;21(2):317-322.

117. Bondy G et al. “Immunomodulation by fungal toxins.” J. of Toxicol. & Environ. Health, Part B. 2000;3(2):109-143.

118. Berek L et al. “Effects of mycotoxins on human immune functions in vitro.” Toxicol. In Vitro February 2001;15(1):25-30.

119. Singer R. Neurotoxicity Guidebook, Van Nostrand Reinold, New York City, 1990.

120. Gray M et al. “Molds, Mycotoxins and Public Health: Summary of 195 patients treated collaboratively.” Presented 11/11/2002 at the American Public Health Assoc. (APHA) meeting in Philadelphia, Pennsylvania.

121. Simon T. “Neurotoxicity- Mold Exposure Versus All Causes.” Presented at the 21st Annual Symposium on Man and His Environment in Health and Disease, Dallas, Texas. June 19-22, 2003.

122. Gordon W et al. “Cognitive impairment associated with exposure to toxigenic fungi.” Presented at the 3rd International Conference on Fungi, Mycotoxins and Bioaerosols- September 23-5, 1998, Saratoga Springs, New York. In Bioaerosols, Fungi and Mycotoxins: Health Effects. Assessments, Prevention and Control, Eastern New York Center for Environmental & Occupational Health, Albany, New York 1999.

123. Didricksen N. “Neurocognitive Deficits in Individuals Exposed to Toxigenic Molds.” Presented at the 21st Annual Symposium on Man and His Environment in Health and Disease, Dallas, Texas. June 19-22, 2003

124. Baldo JV et al. “Neuro-psychological performance of patients following mold exposure.” Applied Neuropsychol. 2002;9(4):193-202.

125. Anyanwu E et al. “Neurophysiological effects of chronic indoor environmental toxic mold exposure on children.” Scientific World J. April 28, 2003;3(4):281-290.

126. Krogh P et al. “Occurrence of ochratoxin A and citrinin in cereals associated with mycotoxic porcine nephropathy.” Acta Path Micro Scand 1973;81 Sect B: 689-695.

127. Castegnaro M et al (eds), Mycotoxins, Endemic Nephropathy and Urinary Tract Tumors. IARC Sci Publication 1991;115:1-340.

128. Groll AH et al. “Trends in the postmortem epidemiology of invasive fungi at a university hospital.” J. of Infection 1996;33:23-32.

129. Husain S et al. “Opportunistic mycelial fungal infections in organ transplant recipients: emerging importance of non-Aspergillus fungi.” Clin. & Infectious Diseases July 15, 2003;37(2):221-229.

130. Denning D. Report on a European Science Foundation Workshop on invasive Aspergillosis. October 21-2, 1998, U of Manchester, Manchester, United Kingdom.

131. Kontoyiannis D et al. “Invasive Aspergillosis in 2002: An Update.” Eur. J. of Clin. Microbiol. & Infectious Disease 2002;21:161-172.

132. Denning D. “Therapeutic outcome in invasive aspergillosis.” Clin. & Infectious Diseases September 1996;23(3):608-615.

133. Lin S et al. “Aspergillosis case-fatality rate: systemic review of the literature.” Clin. & Infectious Diseases February 1, 2001; 32(3):358-366.

134. Panackal A et al. “Outbreak of invasive aspergillosis among renal transplant patients.” Transplantation April 15 2003;75(7):1050-3.

135. Oren I et al. “Invasive pulmonary aspergillosis in neutropenic patients during hospital construction: before and after chemoprophylaxis and institution of HEPA filters.” Am. J. of Hematol. April 2001;66(4):257-262.

136. Loo V et al. “Control of construction-associated nosocomial aspergillosis in an antiquated hematology unit.” Infection Control & Hospital Epidemiol. June 1996;17(6):360-4.

137. Iwen P et al. “Airborne fungal spore monitoring in a protective environment during hospital construction, and correlation with outbreak of invasive aspergillosis.” Infection Control & Hospital Epidemiol. May 1994;15(5):303-6.

138. Hahn T et al. “Efficacy of high-efficiency particulate air filtration in preventing aspergillosis in immunocompromised patients with hematologic malignancies.” Infection Control & Hospital Epidemiol. September 2002;23(9):525-531.

139. Cornet M et al. “Efficacy of prevention by high efficiency particulate air filtration or laminar airflow against Aspergillus airborne contamination during hospital renovation.” Infection Control & Hospital Epidemiol. July 1999;20(7):508-513.

140. Withington S et al. “Invasive aspergillosis in severely neutropenic patients over 18 years: impact on intranasal amphotericin B and HEPA filtration.” J. of Hospital Infection January 1998;38(1):11-8.

141. Sheretz RJ et al. “Impact of air filtration on nosocomial Aspergillus infections.” Am. J. of Medicine October 1987;83(4):709-718.

142. Annaisie EJ et al. “Pathogenic Aspergillus species recovered from a hospital water system: a 3 year prospective study.” Clinical & Infectious Diseases March 15 2002;34(6):780-789.

143. Annaisie EJ et al. “Cleaning patient shower facilities: a novel approach to reducing patient exposure to aerosolized Aspergillus species and other opportunistic molds.” Clin. & Infectious Diseases October 15, 2002;35(8):E86-8.

144. Heuser G et al. “Defining Chemical Injury: A Diagnostic Protocol and Profile of Chemically Injured Civilians, Industrial Workers and Gulf War Veterans.” Int. Persp. in Public Health 2000;13:1-16.

145. Marshall L et al. “Identifying and managing adverse environmental effects: 1) taking an exposure history.” Canadian Med. Assoc. J. April 16, 2002;166(8):1049-1055.

146. Dales RE et al. “Indoor air quality and health: validity and determinants of reported home dampness and molds.” Int. J. of Epidemiol. 1997;26:120-124.

147. Higgins BG et al. “Environmental exposure to air pollution and allergens and peak flow changes.” Eur. Resp. J. July 2000;16(1):61-66.

148. Thorn J et al. “Adult-onset asthma is associated with self-reported mold or environmental tobacco smoke in the home.” Allergy 2001;56:287-292.

149. Chen WY et al. “Synergistic effect of multiple indoor allergen sources on atopic symptoms in primary school children.” Environmental Research September 2003;93(1):1-8.

150. Skoner DP. “Viral infection and allergy: lower airway.” Allergy & Asthma Proceedings July-August 2002;23(4):229-232.

151. Fireman P. “Virus-provoked rhinitis in patients who have allergies.” Allergy & Asthma Proceedings March-April 2002;23(2):99-102.

152. Hirsch D et al. “Effect of central air-conditioning and meteorological factors on indoor spore counts.” J. of Allergy & Clinical Immunology July 1978;62(1):22-26.

153. Bernardis P et al. “Injective versus sublingual immunotherapy in Alternaria tenuis allergic patients.” J. of Investigative Allergol. & Clinical Immunol. January-February 1996;6(1):55-62.

154. Helbling A et al. “Immunotherapy in fungal allergy.” Current Allergy & Asthma Reports September 2003;3(5):447-453.

155. Galvano F et al. “Dietary strategies to counteract the effects of mycotoxins: a review.” J. of Food Protection January 2001;64(1):120-131.

156. Atroshi F et al. “Antioxidant nutrients and mycotoxins.” Toxicology November 15, 2002;180(2):151-167.