Association Between the Adiponectin +45T>G Genotype and Risk of Cardiovascular Disease: A Meta-analysis

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Abstract

Background: Numerous studies have investigated the association between adiponectin +45 nucleotide T/G (+45T>G) polymorphisms and cardiovascular disease (CVD). However, these studies have been inconclusive because of obvious inconsistencies among results. The present study aims to quantify the strength of the association between +45T>G (rs2241766) in the adiponectin gene and the risk of CVD. Methods: We searched the PubMed, Embase, and Wangfang databases for studies related to the association between the adiponectin +45T>G genotype and the risk of CVD. We estimated the summary odds ratio (OR) with 95% confidence interval (CI) to assess the association. Results: A total of 28 case-control studies, with 12,378 CVD cases and 19,368 controls, were included in the meta-analysis. The meta-analysis of the 28 studies showed that the single-nucleotide polymorphism (SNP) +45T>G genotype was associated with an increased risk of CVD (random-effects OR. =. 1.22, 95% CI 1.08-1.39, p=. 0.002). After adjusting for heterogeneity, the meta-analysis showed that the SNP +45T>G genotype was associated with the risk of CVD in the analyses of the total population and the Caucasian population (for the total population, fixed-effects OR. =. 1.11, 95% CI 1.01-1.23, p=. 0.012; for the Caucasian population, fixed-effects OR. =. 1.16, 95% CI 1.01-1.34, p=. 0.039). No significant association was found in other populations. Evidence of publication bias was observed in the meta-analysis. Conclusion: A significant association between rs2241766 in the adiponectin gene and CVD was established by the meta-analysis. © 2013 Australian and New Zealand Society of Cardiac and Thoracic Surgeons (ANZSCTS) and the Cardiac Society of Australia and New Zealand (CSANZ).

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Zhou, D., Jin, Y., Yao, F., Duan, Z., Wang, Q., & Liu, J. (2014). Association Between the Adiponectin +45T>G Genotype and Risk of Cardiovascular Disease: A Meta-analysis. Heart Lung and Circulation, 23(2), 159–165. https://doi.org/10.1016/j.hlc.2013.07.010

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