Department of Geriatrics, First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
PLoS One. 2012;7(4):e33511. doi: 10.1371/journal.pone.0033511. Epub 2012 Apr 4.
The polymorphism of plasminogen activator inhibitor-1 (PAI-1) 4G/5G gene has been indicated to be correlated with coronary artery disease (CAD) susceptibility, but study results are still debatable.
The present meta-analysis was performed to investigate the association between PAI-1 4G/5G gene polymorphism and CAD in the Chinese Han population. A total of 879 CAD patients and 628 controls from eight separate studies were involved. The pooled odds ratio (OR) for the distribution of the 4G allele frequency of PAI-1 4G/5G gene and its corresponding 95% confidence interval (CI) was assessed by the random effect model.
The distribution of the 4 G allele frequency was 0.61 for the CAD group and 0.51 for the control group. The association between PAI-1 4G/5G gene polymorphism and CAD in the Chinese Han population was significant under an allelic genetic model (OR = 1.70, 95% CI = 1.18 to 2.44, P = 0.004). The heterogeneity test was also significant (P<0.0001). Meta-regression was performed to explore the heterogeneity source. Among the confounding factors, the heterogeneity could be explained by the publication year (P = 0.017), study region (P = 0.014), control group sample size (P = 0.011), total sample size (P = 0.011), and ratio of the case to the control group sample size (RR) (P = 0.019). In a stratified analysis by the total sample size, significantly increased risk was only detected in subgroup 2 under an allelic genetic model (OR = 1.93, 95% CI = 1.09 to 3.35, P = 0.02).
In the Chinese Han population, PAI-1 4G/5G gene polymorphism was implied to be associated with increased CAD risk. Carriers of the 4G allele of the PAI-1 4G/5G gene might predispose to CAD.
纤溶酶原激活物抑制剂-1(PAI-1)4G/5G 基因多态性与冠状动脉疾病(CAD)易感性相关,但研究结果仍存在争议。
本荟萃分析旨在研究 PAI-1 4G/5G 基因多态性与中国汉族人群 CAD 之间的关系。共纳入 8 项独立研究的 879 例 CAD 患者和 628 例对照。采用随机效应模型评估 PAI-1 4G/5G 基因 4G 等位基因频率的分布及相应的 95%置信区间(CI)的合并优势比(OR)。
CAD 组 4G 等位基因频率为 0.61,对照组为 0.51。在等位基因遗传模型下,PAI-1 4G/5G 基因多态性与中国汉族人群 CAD 之间存在显著相关性(OR=1.70,95%CI=1.18 至 2.44,P=0.004)。异质性检验也具有统计学意义(P<0.0001)。进行了荟萃回归分析以探索异质性来源。在混杂因素中,可通过发表年份(P=0.017)、研究区域(P=0.014)、对照组样本量(P=0.011)、总样本量(P=0.011)和病例对照样本量比(RR)(P=0.019)来解释异质性。按总样本量进行分层分析,仅在等位基因遗传模型下的亚组 2 中发现显著增加的风险(OR=1.93,95%CI=1.09 至 3.35,P=0.02)。
在中国汉族人群中,PAI-1 4G/5G 基因多态性与 CAD 风险增加相关。PAI-1 4G/5G 基因 4G 等位基因携带者可能易患 CAD。