Department of Cardiology, Chongqing Medical University, Chongqing, 400016, China.
Mol Biol Rep. 2013 Mar;40(3):2589-98. doi: 10.1007/s11033-012-2345-x. Epub 2012 Dec 16.
The potential relationship between Interleukin-6 (IL-6) gene polymorphisms and coronary artery disease (CAD) has been widely investigated. However, study findings on the -174 G/C and -572 G/C variants remain inconsistent and somewhat controversial. The present meta-analysis was conducted in an attempt to provide a more robust synthesis conclusion. PubMed and Embase were used to search for all relevant studies published on or before May 22, 2012. A total of 19 studies were ultimately included in the analysis. Overall combined risk was calculated with fixed or random-effects models. Subgroup and sensitivity analyses were performed. Among the included studies, no statistically significant differences were found between controls and CAD cases for the G allele contrasts of the -174 G/C and -572 G/C polymorphisms. The co-dominant genetic model was evaluated for the -174 G/C polymorphism. A significant association was detected using GG versus CC (OR = 0.801, 95 % CI: [0.652, 0.983], P = 0.034). However, the association was not obviously in subgroup analysis by ethnicity. The recessive genetic model was evaluated for the -572 G/C polymorphism. The relationship between -572 G/C polymorphism and CAD risk was only found to be significant in Asian populations (random-effects: OR = 1.908, 95 % CI: [1.016, 3.581], P = 0.044) using GG versus GC+CC. No obvious publication bias was found by Begg's funnel plots and the Egger's linear regression test (P = 0.315 for -174 G/C polymorphism and P = 0.118 for -572 G/C polymorphism). Our study indicated that the association between the IL-6 gene and CAD risk was mild and moderate for the -174 G/C and -572 G/C polymorphisms. However, this relationship requires additional investigation through well-designed studies with larger sample sizes.
白细胞介素-6(IL-6)基因多态性与冠状动脉疾病(CAD)之间的潜在关系已得到广泛研究。然而,关于-174 G/C 和-572 G/C 变体的研究结果仍不一致,存在一定争议。本荟萃分析旨在提供更有力的综合结论。使用 PubMed 和 Embase 搜索截至 2012 年 5 月 22 日发表的所有相关研究。共有 19 项研究最终纳入分析。使用固定或随机效应模型计算总体合并风险。进行了亚组和敏感性分析。在纳入的研究中,对于-174 G/C 和-572 G/C 多态性的 G 等位基因对照,对照组与 CAD 病例之间未发现统计学显著差异。对于-174 G/C 多态性,评估了共显性遗传模型。发现 GG 与 CC 相比(OR=0.801,95%CI:[0.652,0.983],P=0.034)存在显著关联。然而,按种族进行的亚组分析中,这种关联并不明显。对于-572 G/C 多态性,评估了隐性遗传模型。仅在亚洲人群中发现-572 G/C 多态性与 CAD 风险之间存在显著关系(随机效应:OR=1.908,95%CI:[1.016,3.581],P=0.044),GG 与 GC+CC 相比。Begg 漏斗图和 Egger 线性回归检验未发现明显的发表偏倚(-174 G/C 多态性的 P=0.315,-572 G/C 多态性的 P=0.118)。本研究表明,IL-6 基因与 CAD 风险之间的关联对于-174 G/C 和-572 G/C 多态性为轻度到中度。然而,这种关系需要通过设计更好、样本量更大的研究进一步研究。