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Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population

OBJECTIVE: To explore the potential association between asbestos exposure and risk of autoimmune disease, we conducted a case–control study among a cohort of 7,307 current and former residents of Libby, Montana, a community with historical occupational and environmental exposure to asbestos-contamin...

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Autores principales: Noonan, Curtis W., Pfau, Jean C., Larson, Theodore C., Spence, Michael R.
Formato: Texto
Lenguaje:English
Publicado: National Institute of Environmental Health Sciences 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1551997/
https://www.ncbi.nlm.nih.gov/pubmed/16882533
http://dx.doi.org/10.1289/ehp.9203
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author Noonan, Curtis W.
Pfau, Jean C.
Larson, Theodore C.
Spence, Michael R.
author_facet Noonan, Curtis W.
Pfau, Jean C.
Larson, Theodore C.
Spence, Michael R.
author_sort Noonan, Curtis W.
collection PubMed
description OBJECTIVE: To explore the potential association between asbestos exposure and risk of autoimmune disease, we conducted a case–control study among a cohort of 7,307 current and former residents of Libby, Montana, a community with historical occupational and environmental exposure to asbestos-contaminated vermiculite. METHODS: Cases were defined as those who reported having one of three systemic autoimmune diseases (SAIDs): systemic lupus erythematosus, scleroderma, or rheumatoid arthritis (RA). Controls were randomly selected at a 3:1 ratio from among the remaining 6,813 screening participants using frequency-matched age and sex groupings. RESULTS: The odds ratios (ORs) and 95% confidence intervals (CIs) for SAIDs among those ≥ 65 years of age who had worked for the vermiculite mining company were 2.14 (95% CI, 0.90–5.10) for all SAIDs and 3.23 (95% CI, 1.31–7.96) for RA. In this age group, exposure to asbestos while in the military was also an independent risk factor, resulting in a tripling in risk. Other measures of occupational exposure to vermiculite indicated 54% and 65% increased risk for SAIDs and RA, respectively. Those who had reported frequent contact with vermiculite through various exposure pathways also demonstrated elevated risk for SAIDs and RA. We found increasing risk estimates for SAIDs with increasing numbers of reported vermiculite exposure pathways (p < 0.001). CONCLUSION: These preliminary findings support the hypothesis that asbestos exposure is associated with autoimmune disease. Refined measurements of asbestos exposure and SAID status among this cohort will help to further clarify the relationship between these variables.
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spelling pubmed-15519972006-08-29 Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population Noonan, Curtis W. Pfau, Jean C. Larson, Theodore C. Spence, Michael R. Environ Health Perspect Research OBJECTIVE: To explore the potential association between asbestos exposure and risk of autoimmune disease, we conducted a case–control study among a cohort of 7,307 current and former residents of Libby, Montana, a community with historical occupational and environmental exposure to asbestos-contaminated vermiculite. METHODS: Cases were defined as those who reported having one of three systemic autoimmune diseases (SAIDs): systemic lupus erythematosus, scleroderma, or rheumatoid arthritis (RA). Controls were randomly selected at a 3:1 ratio from among the remaining 6,813 screening participants using frequency-matched age and sex groupings. RESULTS: The odds ratios (ORs) and 95% confidence intervals (CIs) for SAIDs among those ≥ 65 years of age who had worked for the vermiculite mining company were 2.14 (95% CI, 0.90–5.10) for all SAIDs and 3.23 (95% CI, 1.31–7.96) for RA. In this age group, exposure to asbestos while in the military was also an independent risk factor, resulting in a tripling in risk. Other measures of occupational exposure to vermiculite indicated 54% and 65% increased risk for SAIDs and RA, respectively. Those who had reported frequent contact with vermiculite through various exposure pathways also demonstrated elevated risk for SAIDs and RA. We found increasing risk estimates for SAIDs with increasing numbers of reported vermiculite exposure pathways (p < 0.001). CONCLUSION: These preliminary findings support the hypothesis that asbestos exposure is associated with autoimmune disease. Refined measurements of asbestos exposure and SAID status among this cohort will help to further clarify the relationship between these variables. National Institute of Environmental Health Sciences 2006-08 2006-05-30 /pmc/articles/PMC1551997/ /pubmed/16882533 http://dx.doi.org/10.1289/ehp.9203 Text en http://creativecommons.org/publicdomain/mark/1.0/ Publication of EHP lies in the public domain and is therefore without copyright. All text from EHP may be reprinted freely. Use of materials published in EHP should be acknowledged (for example, ?Reproduced with permission from Environmental Health Perspectives?); pertinent reference information should be provided for the article from which the material was reproduced. Articles from EHP, especially the News section, may contain photographs or illustrations copyrighted by other commercial organizations or individuals that may not be used without obtaining prior approval from the holder of the copyright.
spellingShingle Research
Noonan, Curtis W.
Pfau, Jean C.
Larson, Theodore C.
Spence, Michael R.
Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population
title Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population
title_full Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population
title_fullStr Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population
title_full_unstemmed Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population
title_short Nested Case–Control Study of Autoimmune Disease in an Asbestos-Exposed Population
title_sort nested case–control study of autoimmune disease in an asbestos-exposed population
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1551997/
https://www.ncbi.nlm.nih.gov/pubmed/16882533
http://dx.doi.org/10.1289/ehp.9203
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