Seven functional polymorphisms in the CETP gene and myocardial infarction risk: a meta-analysis and meta-regression.

Bibliographic Details
Title: Seven functional polymorphisms in the CETP gene and myocardial infarction risk: a meta-analysis and meta-regression.
Authors: Qi Wang, Shao-Bo Zhou, Li-Jie Wang, Ming-Ming Lei, Yong Wang, Chi Miao, Yuan-Zhe Jin
Source: PLoS ONE, Vol 9, Iss 2, p e88118 (2014)
Publisher Information: Public Library of Science (PLoS), 2014.
Publication Year: 2014
Collection: LCC:Medicine
LCC:Science
Subject Terms: Medicine, Science
More Details: OBJECTIVE: This meta-analysis aims to evaluate the relationships between seven functional polymorphisms in the CETP gene and myocardial infarction (MI) risk. METHOD: The PubMed, CISCOM, CINAHL, Web of Science, Google Scholar, EBSCO, Cochrane Library, and CBM databases were searched for relevant articles published before March 1st, 2013 without any language restrictions. Meta-analysis was conducted using the STATA 12.0 software. RESULTS: Nine case-control studies with a total 8,623 MI cases and 8,564 healthy subjects met the inclusion criteria. The results of our meta-analysis suggested that CETP rs708272 (C>T) polymorphism might be correlated with an increased risk of MI, especially among Caucasians. Furthermore, we observed that CETP rs1800775 (C>A) polymorphism might increase the risk of MI. Nevertheless, no similar findings were found for CETP rs5882 (A>G), rs2303790 (A>G), rs1800776 (C>A), rs12149545 (G>A), and rs4783961 (G>A) polymorphisms. CONCLUSION: The current meta-analysis suggests that CETP rs708272 (C>T) and rs1800775 (C>A) polymorphisms may contribute to MI susceptibility, especially among Caucasians. Thus, CETP rs708272 and rs1800775 polymorphisms may be promising and potential biomarkers for early diagnosis of MI.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1932-6203
Relation: http://europepmc.org/articles/PMC3922770?pdf=render; https://doaj.org/toc/1932-6203
DOI: 10.1371/journal.pone.0088118
Access URL: https://doaj.org/article/e38d44e807f740599053c46d7f06c663
Accession Number: edsdoj.38d44e807f740599053c46d7f06c663
Database: Directory of Open Access Journals
More Details
ISSN:19326203
DOI:10.1371/journal.pone.0088118
Published in:PLoS ONE
Language:English