rantes gene g-403a polymorphism and coronary artery disease a meta analysis of observational studies咆哮基因g - 403 a多态性和冠状动脉疾病的观察性研究的meta分析.pdfVIP
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rantes gene g-403a polymorphism and coronary artery disease a meta analysis of observational studies咆哮基因g - 403 a多态性和冠状动脉疾病的观察性研究的meta分析
RANTES Gene G-403A Polymorphism and Coronary
Artery Disease: A Meta Analysis of Observational Studies
Jun Liu, Yan-Jun Jia, Xiao-Lin Li, Rui-Xa Xu, Cheng-Gang Zhu, Yuan-Lin Guo, Na-Qiong Wu, Jian-Jun Li*
Division of Dyslipidemia, State Key Laboratory of Cardiovascular Disease, Fu Wai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical
Sciences, Peking Union Medical College, Beijing, China
Abstract
Objective: The G-403A polymorphism in RANTES gene may be involved in the development of coronary artery disease
(CAD) through increasing RANTES-mediated leukocyte trafficking and activation. However, studies investigating the
relationship between G-403A polymorphism and CAD yielded contradictory and inconclusive results. In order to shed some
light on these inconsistent findings, a meta analysis was performed to clarify the role of G-403A polymorphism of RANTES
gene in the susceptibility of CAD.
Methods: A systemic literature search of PubMed and EMBASE was conducted from their inception to March 23, 2012, to
retrieve related studies. In addition, Conference Proceedings Citation Index-Science was searched, authors of relevant
studies were contacted, and reference lists of the included studies and their related citations in PubMed were reviewed for
additional pertinent studies.
Results: A total of 8 eligible studies were identified, with a total of 4252 CAD cases and 2150 controls. There was no
evidence of significant association between G-403A polymorphism and CAD risk in any genetic model or pairwise
comparisons (additive model: OR = 1.046, 95% CI = 0.883–1.239, I2 = 65.9%; recessive model: OR = 1.140, 95% CI = 0.774–
1.678, I2 = 53.1%; dominant model: OR = 1.000, 95% CI = 0.820–1.21), I2 = 62.6%; AA v
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