Accelerated spirometric decline in New York City firefighters with alpha 1-antitrypsin deficiency
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2010/11/01
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Details
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Personal Author:Banauch GI ; Brantly M ; Chavko R ; Christodoulou V ; Hall C ; Izbicki G ; Prezant DJ ; Santhyadka G ; Shanske A ; Weiden MD
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Description:BACKGROUND: On September 11, 2001, the World Trade Center (WTC) collapse caused massive air pollution, producing variable amounts of lung function reduction in the New York City Fire Department (FDNY) rescue workforce. alpha1-Antitrypsin (AAT) deficiency is a risk factor for obstructive airway disease. METHODS: This prospective, longitudinal cohort study of the first 4 years post-September 11, 2001, investigated the influence of AAT deficiency on adjusted longitudinal spirometric change (FEV1) in 90 FDNY rescue workers with WTC exposure. Workers with protease inhibitor (Pi) Z heterozygosity were considered moderately AAT deficient. PiS homozygosity or PiS heterozygosity without concomitant PiZ heterozygosity was considered mild deficiency, and PiM homozygosity was considered normal. Alternately, workers had low AAT levels if serum AAT was = 20 µmol/L. RESULTS: In addition to normal aging-related decline (37 mL/y), significant FEV(1) decline accelerations developed with increasing AAT deficiency severity (110 mL/y for moderate and 32 mL/y for mild) or with low AAT serum levels (49 mL/y). Spirometric rates pre-September 11, 2001, did not show accelerations with AAT deficiency. Among workers with low AAT levels, cough persisted in a significant number of participants at 4 years post-September 11, 2001. CONCLUSIONS: FDNY rescue workers with AAT deficiency had significant spirometric decline accelerations and persistent airway symptoms during the first 4 years after WTC exposure, representing a novel gene-by-environment interaction. Clinically meaningful decline acceleration occurred even with the mild serum AAT level reductions associated with PiS heterozygosity (without concomitant PiZ heterozygosity). [Description provided by NIOSH]
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ISSN:0012-3692
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Volume:138
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Issue:5
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NIOSHTIC Number:nn:20038127
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Citation:Chest 2010 Nov; 138(5):1116-1124
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Contact Point Address:Gisela I. Banauch, MD, Division of Pulmonary, Allergy, Critical Care and Sleep Medicine, Room S6-842, University of Massachusetts Memorial Hospital Center, 55 Lake Ave N, Worcester, MA 01655
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Email:banauchg@ummhc.org
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Federal Fiscal Year:2011
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Performing Organization:New York City Fire Department
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Peer Reviewed:True
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Start Date:20040701
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Source Full Name:Chest
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End Date:20110630
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Main Document Checksum:urn:sha-512:be263626c100151cc1e704170b433c8cef7fc8012d24f9f36cac23d7cf9fd204194d2a9413daec0e6211c73b84c2f69572d75c350a5e81dc2d0698a28672efbb
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