Meta-analyses on Suspected Chronic Obstructive Pulmonary Disease Genes: A Summary of 20 Years' Research
Chronic obstructive pulmonary disease (COPD) is a complex disorder with high mortality worldwide. Studies on the role of candidate genes and their polymorphisms in COPD development have so far produced ambiguous results. The aim of this study was to reveal the role of COPD candidate genes using data...
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Published in | American journal of respiratory and critical care medicine Vol. 180; no. 7; pp. 618 - 631 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
New York, NY
Am Thoracic Soc
01.10.2009
American Thoracic Society |
Subjects | |
Online Access | Get full text |
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Summary: | Chronic obstructive pulmonary disease (COPD) is a complex disorder with high mortality worldwide. Studies on the role of candidate genes and their polymorphisms in COPD development have so far produced ambiguous results.
The aim of this study was to reveal the role of COPD candidate genes using data collected in previous research.
We performed meta-analyses on 20 polymorphisms in 12 genes, after searching the PubMed and Embase databases for publications on COPD. These genes involve three main pathways associated with COPD development: the inflammatory, protease-antiprotease balance, and antioxidant pathways.
We obtained significant results for three TGFB1 polymorphisms, although these were based only on a few studies. The IL1RN VNTR polymorphism increases the risk for COPD (odds ratio [OR], 1.7; 95% confidence interval [CI], 1.09-2.65), whereas the TNFA -308 G/A polymorphism does so only in Asian populations (OR, 2.01; 95% CI, 1.21-3.31). The GSTP1 I105V polymorphism was protective for COPD in Asian populations only (OR, 0.69; 95% CI, 0.56-0.85).
These results demonstrate the importance of ethnicity in identifying specific COPD genes. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ISSN: | 1073-449X 1535-4970 1535-4970 |
DOI: | 10.1164/rccm.200905-0722OC |