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白细胞介素-6 基因多态性与冠心病的关联:一项更新的系统评价和累积荟萃分析。

Association of interleukin-6 gene polymorphism with coronary artery disease: an updated systematic review and cumulative meta-analysis.

机构信息

Taishan Medical University, No. 2 YingSheng East Road, Taian, 271000, People's Republic of China,

出版信息

Inflamm Res. 2015 Sep;64(9):707-20. doi: 10.1007/s00011-015-0850-9. Epub 2015 Jul 15.

Abstract

BACKGROUND

Interleukin-6 (IL-6) is an important mediator of atherosclerotic disease and is also associated with coronary artery disease (CAD). The growing evidences suggest that polymorphisms in the IL-6 promoter region influence the progression of CAD. This study was performed to update the systematic results of association of IL-6 gene polymorphisms with CAD.

METHODS

PubMed, Embase, and China Biology Medicine were searched systematically for English and Chinese articles published up to October 31, 2014. Data were extracted using standardized forms. Odds ratios (ORs) with 95 % confidence intervals (CIs) were used to assess the strength of associations. Subgroup analyses were made on ethnicity.

RESULTS

A total of 42 studies including 15,145 cases and 21,496 controls were combined in this meta-analysis. IL-6 gene -174G/C polymorphism was associated with an increased risk of CAD (for C allele versus G allele: OR = 1.11, 95 % CI 1.02-1.20; for C/C versus G/G: OR = 1.21, 95 % CI 1.03-1.42; for C/C + C/G versus G/G: OR = 1.14, 95 % CI 1.03-1.27). In the subgroup analyses based on ethnicity, a significant association was found between -174 G/C polymorphism and CAD in Caucasians (for C allele versus G allele: OR = 1.12, 95 % CI 1.03-1.22; for C/C versus G/G: OR = 1.21, 95 % CI 1.02-1.42; for C/C + C/G versus G/G: OR = 1.16, 95 % CI 1.05-1.29). In order to reduce heterogeneity, we removed the outlier studies by a Galbraith plot analysis. As a result, the pooled ORs demonstrated no association of -174G/C polymorphism and CAD (C allele versus G allele: OR = 1.02, 95 % CI 0.97-1.06, p = 0.48; C/C versus G/G: OR = 0.1.03, 95 % CI 0.94-1.13, p = 0.48; C/G + C/C versus G/G: OR = 1.03, 95 % CI 0.96-1.09, p = 0.41; C/C versus C/G + G/G: OR = 1.02, 95 % CI 0.94-1.10, p = 0.70, respectively). The polymorphism of -572 G/C was not associated with CAD significantly (for C allele versus G allele: OR = 0.86, 95 % CI 0.74-1.01; C/C versus G/G: OR = 0.99, 95 % CI 0.43-2.27; C/G + C/C versus G/G: OR = 0.96, 95 % CI 0.80-1.15, respectively). In addition, subgroup analyses showed an association between -572 G/C polymorphism and CAD risk among Chinese (C allele versus G allele: OR = 0.64, 95 % CI 0.48-0.85; C/C versus G/G: OR = 0.38, 95 % CI 0.18-0.81; C/G + C/C versus G/G: OR = 0.47, 95 % CI 0.22-1.00; C/C versus C/G + G/G: OR = 0.58, 95 % CI 0.42-0.81).

CONCLUSION

The C allele of -174G/C polymorphism may associate with increased sensibility to CAD among Caucasians in overall analysis. Nevertheless, the effect is interfered by heterogeneity across the included studies. The C allele of -572G/C polymorphism may decrease the risk of CAD in Chinese.

摘要

背景

白细胞介素 6(IL-6)是动脉粥样硬化疾病的重要介质,也与冠状动脉疾病(CAD)相关。越来越多的证据表明,IL-6 启动子区域的多态性影响 CAD 的进展。本研究旨在更新与 CAD 相关的 IL-6 基因多态性的系统结果。

方法

系统检索了 PubMed、Embase 和中国生物医学文献数据库,截至 2014 年 10 月 31 日,检索了英文和中文文献。使用标准化表格提取数据。使用比值比(ORs)及其 95 %置信区间(CIs)来评估关联的强度。进行了亚组分析以评估种族差异。

结果

本荟萃分析共纳入了 42 项研究,包括 15145 例病例和 21496 例对照。IL-6 基因-174G/C 多态性与 CAD 风险增加相关(对于 C 等位基因与 G 等位基因:OR=1.11,95 %CI 1.02-1.20;对于 C/C 与 G/G:OR=1.21,95 %CI 1.03-1.42;对于 C/C+C/G 与 G/G:OR=1.14,95 %CI 1.03-1.27)。基于种族的亚组分析显示,-174G/C 多态性与高加索人 CAD 之间存在显著关联(对于 C 等位基因与 G 等位基因:OR=1.12,95 %CI 1.03-1.22;对于 C/C 与 G/G:OR=1.21,95 %CI 1.02-1.42;对于 C/C+C/G 与 G/G:OR=1.16,95 %CI 1.05-1.29)。为了减少异质性,我们通过 Galbraith 图分析剔除了离群值研究。结果显示,-174G/C 多态性与 CAD 之间无关联(C 等位基因与 G 等位基因:OR=1.02,95 %CI 0.97-1.06,p=0.48;C/C 与 G/G:OR=0.1.03,95 %CI 0.94-1.13,p=0.48;C/G+C/C 与 G/G:OR=1.03,95 %CI 0.96-1.09,p=0.41;C/C 与 C/G+G/G:OR=1.02,95 %CI 0.94-1.10,p=0.70)。-572G/C 多态性与 CAD 无显著相关性(对于 C 等位基因与 G 等位基因:OR=0.86,95 %CI 0.74-1.01;C/C 与 G/G:OR=0.99,95 %CI 0.43-2.27;C/G+C/C 与 G/G:OR=0.96,95 %CI 0.80-1.15)。此外,亚组分析显示,-572G/C 多态性与中国人 CAD 风险之间存在关联(对于 C 等位基因与 G 等位基因:OR=0.64,95 %CI 0.48-0.85;C/C 与 G/G:OR=0.38,95 %CI 0.18-0.81;C/G+C/C 与 G/G:OR=0.47,95 %CI 0.22-1.00;C/C 与 C/G+G/G:OR=0.58,95 %CI 0.42-0.81)。

结论

总体分析显示,-174G/C 多态性的 C 等位基因可能与高加索人 CAD 的敏感性增加有关。然而,这种效应受到纳入研究之间异质性的干扰。-572G/C 多态性的 C 等位基因可能降低中国人 CAD 的风险。

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