Literature DB >> 23489345

Serum total adiponectin level and the risk of cardiovascular disease in general population: a meta-analysis of 17 prospective studies.

Guang Hao1, Wei Li, Rui Guo, Jin-Gang Yang, Yang Wang, Yu Tian, Man-Yun Liu, Ya-Guang Peng, Zeng-Wu Wang.   

Abstract

OBJECTIVE: Many studies have assessed the association between serum adiponectin and the risk of cardiovascular disease (CVD), yet whether adiponectin is an independent risk factor for CVD remains controversial. We performed a meta-analysis of 17 prospective epidemiologic studies to evaluate this relationship in the general population.
METHODS: PubMed and Embase databases were searched through June 2012 to identify studies meeting a priori inclusion criteria, in addition to conducting a secondary reference review. Two principle investigators respectively extracted the information with either fixed-effect model or random-effect model to calculate the relationship between adiponectin and the risk of CVD.
RESULTS: We summarized 17 prospective studies with a total of 23,717 participants. Overall, higher serum adiponectin was related to an increased risk of ischemic stroke: pooled risk ratio (RR) of 1.34 [95% confidence intervals (CI): 1.06-1.69] with no heterogeneity (Q = 1.23; P = 0.541). Serum adiponectin was not related to coronary heart disease (CHD) or CVD: pooled RR of 0.96 (95% CI: 0.85-1.08) and 1.00 (95% CI: 0.89-1.13), respectively.
CONCLUSIONS: Increased serum adiponectin was related to an elevated risk of ischemic stroke, but there was no clear evidence indicating a positive relationship between adiponectin and the risk of CHD or CVD. Crown
Copyright © 2013. Published by Elsevier Ireland Ltd. All rights reserved.

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Year:  2013        PMID: 23489345     DOI: 10.1016/j.atherosclerosis.2013.02.018

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  29 in total

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9.  Temporal and Molecular Analyses of Cardiac Extracellular Matrix Remodeling following Pressure Overload in Adiponectin Deficient Mice.

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