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PHACTR1基因rs9349379和rs12526453多态性与冠状动脉粥样硬化或冠状动脉钙化的关联:一项系统评价。

The association of polymorphism in PHACTR1 rs9349379 and rs12526453 with coronary artery atherosclerosis or coronary artery calcification. A systematic review.

作者信息

Koitsopoulos Pavlos G, Rabkin Simon W

机构信息

Faculty of Medicine.

Department of Medicine (Cardiology), University of British Columbia, Vancouver, Canada.

出版信息

Coron Artery Dis. 2021 Aug 1;32(5):448-458. doi: 10.1097/MCA.0000000000000942.

DOI:10.1097/MCA.0000000000000942
PMID:33660664
Abstract

OBJECTIVE

There is a need to identify genetic factors that may produce coronary artery atherosclerotic disease (CAD) that are not involved in the usual risk factors leading to CAD. Previous studies have often equated coronary artery calcification (CAC) with CAD with coronary stenosis or its sequelae. The objective of this study was to examine the relationship between phosphatase and actin regulator 1 (PHACTR1) single nucleotide polymorphisms (SNPs) and the type of coronary artery disease CAD versus CAC.

METHOD

A systematic review of the literature was conducted to answer the question of whether PHACTR1 gene polymorphisms are associated with coronary artery disease expressed as coronary artery atherosclerosis or CAC.

RESULTS

Eighteen studies spanning seven PHACTR1 SNPs were identified and evaluated for the relationship between PHACTR1 and coronary artery disease. There were significant relationships between rs9349379, rs12526453, and CAD with odds ratios (ORs) (confidence interval) of, respectively, 1.15 (1.13-1.17), 1.13 (1.09-1.17) but not for rs2026458, 1.03 (0.88-1.19). The OR for CAC was 1.22 (1.18-1.26) for rs9349379 and 1.28 (1.21-1.38) for rs12526453.

CONCLUSIONS

Several PHACTR1 specifically rs9349379 and rs12526453 polymorphisms but not rs2026458, are associated with CAD. There are differences in the association of PHACTR1 SNPs with CAC. PHACTR1 warrants more attention and study for the prevention and treatment of CAD.

摘要

目的

需要确定可能导致冠状动脉粥样硬化性疾病(CAD)的遗传因素,这些因素不涉及导致CAD的常见风险因素。以往的研究常常将冠状动脉钙化(CAC)与伴有冠状动脉狭窄或其后遗症的CAD等同起来。本研究的目的是探讨磷酸酶与肌动蛋白调节因子1(PHACTR1)单核苷酸多态性(SNP)与冠状动脉疾病CAD和CAC类型之间的关系。

方法

对文献进行系统综述,以回答PHACTR1基因多态性是否与以冠状动脉粥样硬化或CAC表示的冠状动脉疾病相关的问题。

结果

共鉴定了涉及7个PHACTR1 SNP的18项研究,并对PHACTR1与冠状动脉疾病之间的关系进行了评估。rs9349379、rs12526453与CAD之间存在显著关系,优势比(OR)(置信区间)分别为1.15(1.13 - 1.17)、1.13(1.09 - 1.17),但rs2026458与CAD无显著关系,OR为1.03(0.88 - 1.19)。rs9349379的CAC的OR为1.22(1.18 - 1.26),rs12526453的CAC的OR为1.28(1.21 - 1.38)。

结论

几个PHACTR1基因多态性,特别是rs9349379和rs12526453,但不包括rs2026458,与CAD相关。PHACTR1 SNP与CAC的关联存在差异。PHACTR1在CAD的预防和治疗方面值得更多关注和研究。

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