荟萃分析
优势比
冠状动脉疾病
置信区间
内科学
等位基因
医学
胃肠病学
多态性(计算机科学)
遗传模型
遗传学
人口
病例对照研究
生物信息学
生物
基因
环境卫生
作者
Xiaohong Sun,Jide Sun,Dan Zhao,Yanan Song,Lei Yu
摘要
Background Some genetic association studies tried to investigate potential associations of phosphatase and actin regulator 1 (PHACTR1) polymorphisms with coronary artery disease (CAD). However, the results of these studies were not consistent. Thus, we performed the present meta-analysis to explore associations between PHACTR1 polymorphisms and CAD in a larger pooled population. Methods Systematic literature research of PubMed, Web of Science, Embase and CNKI was performed to identify eligible studies. We calculated odds ratios (ORs) and 95% confidence intervals (CIs) to estimate strength of associations. Results Totally 8 studies were included for analyses (10856 cases and 18801 controls). Pooled analyses suggested that rs9349379 polymorphism was significantly associated with CAD in overall population (dominant model: p=0.004, OR=1.39, 95%CI 1.11-1.73, I2 =91%; recessive model: p=0.002, OR=0.63, 95%CI 0.48-0.84, I2 =85%; over-dominant model: p=0.03, OR=0.89, 95%CI 0.80-0.99, I2 =59%; allele model: p=0.0002, OR=1.30, 95%CI 1.13-1.49, I2 =89%), and this significant finding was further confirmed in both Asians and Caucasians. However, no any positive findings were observed for rs2026458 polymorphism in pooled analyses. Conclusions Our meta-analysis suggested that rs9349379 polymorphism might affect individual susceptibility to CAD in both Caucasians and Asians. Future investigations need to explore the underlying molecular mechanisms of our positive findings.
科研通智能强力驱动
Strongly Powered by AbleSci AI