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肿瘤坏死因子-α-308 G/A 和-238 G/A 多态性与糖尿病视网膜病变的相关性:系统评价和更新的荟萃分析。

Association of Tumor Necrosis Factor-Alpha-308 G/A and -238 G/A Polymorphism with Diabetic Retinopathy: A Systematic Review and Updated Meta-Analysis.

机构信息

Department of Ophthalmology, Peking University First Hospital, Beijing, China,

Department of Ophthalmology, Peking University First Hospital, Beijing, China.

出版信息

Ophthalmic Res. 2021;64(6):903-915. doi: 10.1159/000513586. Epub 2020 Dec 4.

Abstract

BACKGROUND

Mounting evidence has suggested that tumor necrosis factor-alpha (TNF-α) can promote the development of diabetic retinopathy (DR), and TNF-α gene variants may influence DR risk. However, the results are quite different.

OBJECTIVES

To comprehensively address this issue, we performed the meta-analysis to evaluate the association of TNF-α-308 G/A and -238 G/A polymorphism with DR.

METHOD

Data were retrieved in a systematic manner and analyzed using STATA Statistical Software. Crude odds ratios (ORs) with 95% confidence intervals (CIs) were used to assess the strength of associations. Allelic and genotypic comparisons between cases and controls were evaluated.

RESULTS

For the TNF-α-308 G/A polymorphism, overall analysis suggested a marginal association with DR (the OR [95% CI] of [GA vs. GG], [GA + AA] vs. GG, and [A vs. G] are 1.21 [1.04, 1.41], 1.20 [1.03, 1.39], and 1.14 [1.01, 1.30], respectively). And the subgroup analysis indicated an enhanced association among the European population. For the TNF-α-238 G/A polymorphism, there was a mild correlation in the entire group (the OR [95% CI] of [GA vs. GG] is 1.55 [1.14, 2.11]), which was strengthened among the Asian population.

CONCLUSION

The meta-analysis suggested that -308 A and -238 A allele in TNF-α gene potentially increased DR risk and showed a discrepancy in different ethnicities.

摘要

背景

越来越多的证据表明肿瘤坏死因子-α(TNF-α)可促进糖尿病视网膜病变(DR)的发生,TNF-α 基因变异可能影响 DR 的发病风险,但结果差异较大。

目的

为全面阐明这一问题,我们进行了荟萃分析以评估 TNF-α-308 G/A 和-238 G/A 多态性与 DR 的相关性。

方法

系统检索数据,并采用 STATA 统计软件进行分析。采用粗 Odds 比(OR)及其 95%置信区间(CI)评估关联强度。比较病例组和对照组的等位基因和基因型。

结果

TNF-α-308 G/A 多态性的总体分析提示与 DR 存在微弱关联([GA 与 GG]、[GA + AA 与 GG]和[A 与 G]的 OR [95%CI]分别为 1.21[1.04,1.41]、1.20[1.03,1.39]和 1.14[1.01,1.30])。亚组分析显示在欧洲人群中关联增强。TNF-α-238 G/A 多态性在全人群中呈轻度相关([GA 与 GG]的 OR [95%CI]为 1.55[1.14,2.11]),在亚洲人群中关联增强。

结论

荟萃分析提示 TNF-α 基因-308 A 和-238 A 等位基因可能增加 DR 发病风险,且在不同种族间存在差异。

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