Guest guest Posted July 15, 2008 Report Share Posted July 15, 2008 Correspondence Is there any relation between moldy building exposure and chronic fatigue syndrome? Journal: Med Hypotheses. 2006 Mar 7; [Epub ahead of print] Authors: Shahriar Gharibzadeh and Sayed Shahabuddin Hoseini Affiliations: Neuromuscular Systems Laboratory, Faculty of Biomedical Engineering, Amirkabir University of Technology, Somayyeh, Hafez, Tehran 15875-4413, Iran, and Faculty of Medicine, Tehran University of Medical Sciences, Enghelab Street, Tehran, Iran Tel.: +9821 6454 2369; fax: +9821 6649 5655. E-Mail: shahab337@... Available online 9 March 2006. It is reported that workers who are employed in moldy buildings, show different symptoms like respiratory difficulties, fatigue, fever and headache. Hirvonen et al. have reported elevated cytokines (interleukin-1, interleukin-6 and tumor necrosis factor a) and nitric oxide (NO) levels in nasal lavage of workers in exposure to moldy buildings. Due to laboratory tests, Aspergillus fumigatus, Trichoderma, Actinomycetes, etc. were detected in indoor air [1]. On the other hand, chronic fatigue syndrome (CFS) is the current name for a disorder characterized by debilitating fatigue and several associated complaints including headache, sleep disorder, low grade fever and concentration difficulties [2]. It is mentioned that post- infectious, immunological, and psychological factors are involved in the syndrome [3]. Researches in patients with CFS have shown a significant elevation in serum levels of interleukin-1 and tumor necrosis factors a and ß [4]. which can result in the appearance of CFS symptoms. Small amounts of circulating cytokines can enter the cerebrospinal fluid and the parenchyma of the brain [5]. Cytokines administered systemically or directly into the central nervous system have shown to alter the activity of hypothalamus, hippocampus, and prefrontal cortex [6]. In addition, elevated nitric oxide levels have been documented in CFS patients. It is hypothesized that NO plays a significant role in pain sensitization, which is seen in these patients [7]. Moreover, excessive NO production is an important factor in pulmonary manifestations including vasodilation, edema and cytotoxicity [1]. It seems from the abovementioned points that, in accordance with the post-infectious theory of CFS, the exposure to moldy conditions may be a trigger for the onset of CFS. Moreover, the working of persons with CFS in moldy conditions may aggravate their symptoms including pulmonary pain and psychoneurological manifestations. Surely, our hypothesis needs to be validated by experimental evaluation. References [1] M.R. Hirvonen, M. Ruotsalainen, M. Roponen, A. Hyvarinen, T. Husman and V.M. Kosma et al., Nitric oxide and proinflammatory cytokines in nasal lavage fluid associated with symptoms and exposure to moldy building microbes, Am J Respir Crit Care Med 160 (1999) (6), pp. 1943-1946. [2] N. Afari and D. Buchwald, Chronic fatigue syndrome: a review, Am J Psychiatry 160 (2003) (2), pp. 221-236. [3] K. Fukuda, S.E. Straus, I. Hickie, M.C. Sharpe, J.G. Dobbins and A. Komaroff, The chronic fatigue syndrome: a comprehensive approach to its definition and study. International Chronic Fatigue Syndrome Study Group, Ann Intern Med 121 (1994) (12), pp. 953-959. [4] A. Linde, B. Andersson, S.B. Svenson, H. Ahrne, M. Carlsson and P. Forsberg et al., Serum levels of lymphokines and soluble cellular receptors in primary Epstein-Barr virus infection and in patients with chronic fatigue syndrome, J Infect Dis 165 (1992) (6), pp. 994-1000. [5] W.A. Banks, A.J. Kastin and E.G. Gutierrez, Interleukin-1 alpha in blood has direct access to cortical brain cells, Neurosci Lett 163 (1993) (1), pp. 41-44. [6] S. Zalcman, J.M. Green-, L. Murray, D.M. Nance, D. Dyck and H. Anisman et al., Cytokine-specific central monoamine alterations induced by interleukin-1, -2 and -6, Brain Res 643 (1994) (1-2), pp. 40-49. [7] J. Nijs, B. Van de Velde and K. De Meirleir, Pain in patients with chronic fatigue syndrome: does nitric oxide trigger central sensitisation?, Med Hypotheses 64 (2005) (3), pp. 558-562. Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.