| Literature DB >> 16278826 |
Sally Chappell1, Leslie Daly, Kevin Morgan, Tamar Guetta Baranes, Josep Roca, Roberto Rabinovich, Ann Millar, Seamas C Donnelly, Vera Keatings, William MacNee, Jan Stolk, Pieter Hiemstra, Massimo Miniati, Simonetta Monti, Clare M O'Connor, Noor Kalsheker.
Abstract
Chronic obstructive pulmonary disease (COPD) is a major cause of mortality and morbidity worldwide. While cigarette smoking is a major cause of COPD, only 15% of smokers develop the disease, indicating major genetic influences. The most widely recognized candidate gene in COPD is SERPINA1, although it has been suggested that SERPINA3 may also play a role. To detect cryptic genetic variants that might contribute to disease, we identified 15 SNP haplotype tags from high-density SNP maps of the two genes and evaluated these SNPs in the largest case-control genetic study of COPD conducted so far. For SERPINA1, six newly identified haplotypes with a common backbone of five SNPs were found to increase the risk of disease by six- to 50-fold, the highest risk of COPD reported to date. In contrast, no haplotype associations for SERPINA3 were identified. 2005 Wiley-Liss, Inc.Entities:
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Year: 2006 PMID: 16278826 DOI: 10.1002/humu.20275
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878