Department of Laboratory Diagnostics, Changzheng Hospital, Second Military Medical University, Shanghai, China.
PLoS One. 2013 May 21;8(5):e63401. doi: 10.1371/journal.pone.0063401. Print 2013.
Previous studies have evaluated the associations of TNF-α, IL-10 gene polymorphisms and susceptibility to pSS, but the results remained controversial. To assess the associations between TNF-α-308, IL-10-1082, -819, -592 polymorphisms and pSS risk, a meta-analysis was conducted.
The available articles were searched in PubMed, EMBASE and MEDLINE. ORs with 95% CIs were calculated to determine the strength of associations by fixed-effects or random-effects models. The data about IL-10-1082, -819, -592 polymorphisms were analyzed in the additive, dominant and recessive modes. The associations between haplotypes of IL-10 gene and susceptibility to pSS were also assessed.
A total of 9 relevant studies were identified in the meta-analyses. TNF-α-308 A allele was significantly associated with pSS (OR = 1.8, 95% CI: 1.53-2.13). The IL-10 -1082 G allele and the genotype "GCC/ATA" were identified as a candidate genetic risk factor for pSS. Under the dominant model for -819 and -582, the overall ORs suggested that individuals with genotype (CC+TC) or (CC+AC) may have a 59% increased risk of pSS in Caucasians population (OR = 1.59, 95% CI:1.09-1.23). Besides, the genotype "ATA/ATA" may be a protective factor against the development of pSS in Caucasians (OR = 0.40, 95% CI:0.19-0.84).
The meta-analysis demonstrated TNF-α-308 A, IL-10-1082 G allele were significantly associated with pSS susceptibility, supporting these alleles were predisposing factors for pSS. In Caucasian population, the genotype "ATA/ATA" may be a protective factors.
先前的研究已经评估了 TNF-α、IL-10 基因多态性与 pSS 易感性的关联,但结果仍存在争议。为了评估 TNF-α-308、IL-10-1082、-819、-592 多态性与 pSS 风险之间的关联,进行了荟萃分析。
在 PubMed、EMBASE 和 MEDLINE 中搜索可用的文章。使用固定效应或随机效应模型计算 ORs 及其 95%CI,以确定关联的强度。以加性、显性和隐性模式分析了 IL-10-1082、-819、-592 多态性的数据。还评估了 IL-10 基因单倍型与 pSS 易感性之间的关联。
荟萃分析共确定了 9 项相关研究。TNF-α-308 A 等位基因与 pSS 显著相关(OR=1.8,95%CI:1.53-2.13)。IL-10-1082 G 等位基因和基因型“GCC/ATA”被鉴定为 pSS 的候选遗传风险因素。在 -819 和 -582 的显性模型下,总体 OR 表明,高加索人群中基因型(CC+TC)或(CC+AC)的个体可能有 59%的 pSS 风险增加(OR=1.59,95%CI:1.09-1.23)。此外,基因型“ATA/ATA”可能是高加索人群中 pSS 发病的保护因素(OR=0.40,95%CI:0.19-0.84)。
荟萃分析表明 TNF-α-308 A、IL-10-1082 G 等位基因与 pSS 易感性显著相关,支持这些等位基因是 pSS 的易感因素。在高加索人群中,基因型“ATA/ATA”可能是一种保护因素。