An Updated Systematic Review and Meta-analysis of Association Between Adiponectin Gene Polymorphisms and Coronary Artery Disease

被引:26
作者
Hou, Haifeng [1 ,2 ]
Ge, Siqi [2 ,3 ]
Zhao, Linlin [4 ]
Wang, Chenglin [1 ]
Wang, Wei [1 ,2 ]
Zhao, Xuezhen [1 ]
Sun, Zheng [1 ]
机构
[1] Taishan Med Univ, 2 YingSheng East Rd, Tai An 271000, Shandong, Peoples R China
[2] Edith Cowan Univ, Sch Med & Hlth Sci, Perth, WA, Australia
[3] Capital Med Univ, Sch Publ Hlth, Beijing Key Lab Clin Epidemiol, Beijing, Peoples R China
[4] Taishan Vocat Coll Nursing, Tai An, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
adiponectin; polymorphism; coronary artery disease; meta-analysis; genetic biomarkers; SINGLE-NUCLEOTIDE POLYMORPHISMS; CARDIOVASCULAR-DISEASE; HEART-DISEASE; INSULIN-RESISTANCE; MYOCARDIAL-INFARCTION; METABOLIC SYNDROME; ADIPOQ RS1501299; BINDING-PROTEIN; RISK; VARIANTS;
D O I
10.1089/omi.2017.0007
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Coronary artery disease (CAD) is a significant contributor to global health burden. Adiponectin gene single nucleotide polymorphisms (SNPs) have been associated with CAD susceptibility, but with inconsistent results across the studies. We present, in this study, an updated meta-analysis to discern the genetic susceptibility of adiponectin SNPs in relation to CAD. PubMed and EMBASE databases were used to identify the relevant published articles using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Pooled odds ratios and 95% confidence intervals were generated to assess the strength of the associations. Thirty-five articles with a total of 28,947 participants (mean age 55.3 years, 11,632 cases/ 17,315 controls, 19,443 males/8353 females, and 1151 persons with unspecified gender data) were included. The dominant, recessive, and additive models were applied. We found that the SNPs +45T>G (rs2241766), -4034A>C (rs822395), and -11391G>A (rs17300539) were linked to CAD development. In addition, +276G> T (rs1501299) SNP was associated with a decreased susceptibility to CAD among Caucasians. We did not find an association between the CAD susceptibility and the -11377C> G (rs266729) SNP. These observations offer new potential genetic biomarker candidates in relation to CAD, and warrant further research in independent world populations.
引用
收藏
页码:340 / 351
页数:12
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