Wang Xiao-Xiong, Chen Tong
a Department of Ophthalmology, National Center of Gerontology , Beijing hospital , Beijing , China.
Immunol Invest. 2018 Jul;47(5):431-442. doi: 10.1080/08820139.2018.1425699. Epub 2018 Apr 12.
The interleukin-2 receptor alpha (IL2RA) gene polymorphisms may be implicated in the genetic susceptibility to multiple sclerosis (MS). This meta-analysis aims to evaluate the relationship of the IL2RA polymorphisms rs2104286 and rs12722489 with MS risk in different populations.
Eligible association studies were identified through search in Pubmed, Medline, Web of Science, and Scopus (end of search: August 2017). Summary odds ratios (ORs) with 95% confidence intervals (CIs) were calculated using random-effects or fixed-effects models. All statistical analyses were two-sided.
Eleven studies including 8608 cases and 9061 controls evaluated rs2104286. The results demonstrated that the A allele of rs2104286 was associated with increased risk of MS in Caucasians (OR = 1.19, 95%CI: 1.13-1.25, p < 0.001) and Asians (OR = 1.25, 95%CI: 1.01-1.55, p = 0.041), respectively. Concerning rs12722489, six studies with 4259 cases and 5420 controls were eligible. We found that the C allele of rs12722489 was associated with elevated MS risk in Caucasians (OR = 1.20, 95% CI: 1.12-1.29, p < 0.001) but not in Asians (OR = 1.10, 95%CI: 0.75-1.63, p = 0.629). Statistical evidence from the Egger and Begg tests showed absence of publication bias. Sensitivity analysis showed that the results were stable.
Our meta-analysis suggests that the rs2104286 A allele is associated with increased MS risk in both Caucasians and Asians, whereas the rs12722489 C allele is associated with elevated MS risk in Caucasians but not in Asians.
白细胞介素-2受体α(IL2RA)基因多态性可能与多发性硬化症(MS)的遗传易感性有关。本荟萃分析旨在评估IL2RA基因多态性rs2104286和rs12722489与不同人群MS风险之间的关系。
通过检索PubMed、Medline、Web of Science和Scopus(检索截止日期:2017年8月)确定符合条件的关联研究。使用随机效应或固定效应模型计算汇总比值比(OR)及其95%置信区间(CI)。所有统计分析均为双侧检验。
11项研究(包括8608例病例和9061例对照)评估了rs2104286。结果表明,rs2104286的A等位基因分别与白种人(OR = 1.19,95%CI:1.13 - 1.25,p < 0.001)和亚洲人(OR = 1.25,95%CI:1.01 - 1.55,p = 0.041)MS风险增加相关。关于rs12722489,6项研究(包括4259例病例和5420例对照)符合条件。我们发现,rs12722489的C等位基因与白种人MS风险升高相关(OR = 1.20,95%CI:1.12 - 1.29,p < 0.001),但与亚洲人无关(OR = 1.10,95%CI:0.75 - 1.63,p = 0.629)。Egger检验和Begg检验的统计证据显示不存在发表偏倚。敏感性分析表明结果稳定。
我们的荟萃分析表明,rs2104286的A等位基因与白种人和亚洲人MS风险增加相关,而rs12722489的C等位基因与白种人MS风险升高相关,但与亚洲人无关。