Jiang N, Yang G, Peng C L
The Third Department of Cardiovascular, The First Hospital Affiliated Heilongjiang University of TCM, Xiangfang, Harbin, Heilongjiang, China.
Genet Mol Res. 2015 Oct 30;14(4):13932-44. doi: 10.4238/2015.October.29.14.
The aim of this meta-analysis was to evaluate the correlations between the estrogen receptor 1 (ESR1) gene polymorphisms PvuII (rs2234693T>C) and XbaI (rs9340799A>G) and the risk of cardiovascular disease (CVD). Case-control studies were screened and selected from a larger group of studies that were retrieved through a comprehensive search of scientific literature databases, which was complemented by manual searches. Data from studies selected were analyzed using the Comprehensive Meta-analysis 2.0 software. A total of 240 studies were initially retrieved and 10 studies were eventually included in the meta-analysis. These 10 case-control studies involved 7029 CVD patients (5001 myocardial infarction patients, 1223 coronary artery disease patients, 805 acute coronary syndromes patients) and 6901 healthy controls. We found no significant association between the PvuII (rs2234693T>C) and XbaI (rs9340799A>G) polymorphisms and CVD risk. We detected no significant associations under all genetic inheritance models tested, including the allele, dominant, homozygous, heterozygous, and recessive models, or for comparisons between the case group and control group (all P > 0.05). Our meta-analysis results strongly suggest that the ESR1 gene polymorphisms PvuII (rs2234693T>C) and XbaI (rs9340799A>G) are not associated with CVD risk.
本荟萃分析的目的是评估雌激素受体1(ESR1)基因多态性PvuII(rs2234693T>C)和XbaI(rs9340799A>G)与心血管疾病(CVD)风险之间的相关性。通过对科学文献数据库进行全面检索,并辅以人工检索,从大量研究中筛选并选取病例对照研究。使用Comprehensive Meta-analysis 2.0软件对所选研究的数据进行分析。最初检索到240项研究,最终10项研究纳入荟萃分析。这10项病例对照研究涉及7029例CVD患者(5001例心肌梗死患者、1223例冠状动脉疾病患者、805例急性冠状动脉综合征患者)和6901例健康对照。我们发现PvuII(rs2234693T>C)和XbaI(rs9340799A>G)多态性与CVD风险之间无显著关联。在所有测试的遗传遗传模型下,包括等位基因、显性、纯合子、杂合子和隐性模型,或病例组与对照组之间的比较中,我们均未检测到显著关联(所有P>0.05)。我们的荟萃分析结果强烈表明,ESR1基因多态性PvuII(rs2234693T>C)和XbaI(rs9340799A>G)与CVD风险无关。