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脂联素基因多态性与高血压风险的关联:系统评价和荟萃分析。

Associations between polymorphisms of the ADIPOQ gene and hypertension risk: a systematic and meta-analysis.

机构信息

Department of Cardiology, Centre Hospital of Xianyang, Xianyang 712000, People's Republic of China.

Department of Clinical Laboratory, The Affiliated Hospital of Yan'an University, Yan'an University, Yan'an 71600, People's Republic of China.

出版信息

Sci Rep. 2017 Feb 9;7:41683. doi: 10.1038/srep41683.

Abstract

ADIPOQ gene polymorphisms have been indicated to be associated with hypertension; however, published studies have reported inconsistent results. Eligible studies were retrieved by searching the PubMed, Embase and China National Knowledge Infrastructure databases. The case group consisted of patients with hypertension, and the control group consisted of subjects with normal blood pressure. Based on eleven published articles, involving 4837 cases and 5618 controls, the pooled results from rs2241766 polymorphism showed increased risk in the allelic model (G VS T: OR = 1.16, 95%CI = 1.06-1.27), recessive model (GG VS GT + TT: OR = 1.34, 95%CI = 1.10-1.63), dominant model (GG + GT VS TT: OR = 1.15, 95%CI = 1.02-1.30) and homozygote model (GG VS TT: OR = 1.38, 95%CI = 1.21-1.69). In addition, rs266729 polymorphism showed increased risk for hypertension in the recessive model (GG VS GC + CC: OR = 1.43, 95%CI = 1.02-2.01). In the Caucasian subgroup, rs1501299 polymorphism showed decreased risk of hypertension in the allelic model (T VS G: OR = 0.75, 95%CI = 0.58-0.97), dominant model (TT + TG VS GG: OR = 0.83, 95%CI = 0.71-0.98) and heterozygote model (TG VS GG: OR = 0.82, 95%CI = 0.68-0.99). The rs2241766 polymorphism was associated with a significant increase in hypertension risk based on our analysis. Moreover, an increased risk of rs266729 in hypertension patients was also detected. Our meta-analysis suggests that the rs1501299 polymorphism may play a protective role in hypertension in Caucasian subgroup; however, this finding requires further study.

摘要

ADIPOQ 基因多态性与高血压有关;然而,已发表的研究结果并不一致。通过检索 PubMed、Embase 和中国知网数据库,检索到符合条件的研究。病例组由高血压患者组成,对照组由血压正常的受试者组成。基于 11 篇已发表的文章,涉及 4837 例病例和 5618 例对照,rs2241766 多态性的汇总结果显示,在等位基因模型(G 对 T:OR=1.16,95%CI=1.06-1.27)、隐性模型(GG 对 GT+TT:OR=1.34,95%CI=1.10-1.63)、显性模型(GG+GT 对 TT:OR=1.15,95%CI=1.02-1.30)和纯合子模型(GG 对 TT:OR=1.38,95%CI=1.21-1.69)中存在风险增加。此外,rs266729 多态性在隐性模型(GG 对 GC+CC:OR=1.43,95%CI=1.02-2.01)中增加了高血压的风险。在白种人亚组中,rs1501299 多态性在等位基因模型(T 对 G:OR=0.75,95%CI=0.58-0.97)、显性模型(TT+TG 对 GG:OR=0.83,95%CI=0.71-0.98)和杂合子模型(TG 对 GG:OR=0.82,95%CI=0.68-0.99)中显示出降低高血压风险的作用。基于我们的分析,rs2241766 多态性与高血压风险显著增加相关。此外,还检测到 rs266729 与高血压患者风险增加相关。我们的荟萃分析表明,rs1501299 多态性可能在白种人亚组中发挥保护作用;然而,这一发现需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62f3/5299502/119c4fc10f95/srep41683-f1.jpg

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