Chen Xuping, Zhou Zhenxing, Zhang Yi, Cheng Xiaoliang, Guo Xiaowen, Yang Xiaodong
Department of Respiratory Medicine, West China Hospital of Sichuan University, Chengdu, Sichuan, China.
Sarcoidosis Vasc Diffuse Lung Dis. 2018;35(2):115-122. doi: 10.36141/svdld.v35i2.6257. Epub 2018 Apr 28.
The association between (nucleotide binding oligomerisation domain containing 2) gene polymorphisms and susceptibility to sarcoidosis have been extensively investigated in recent years. However, the results from previous studies remain controversial. To assess the association of polymorphisms and sarcoidosis susceptibility, we performed a meta-analysis. PubMed, Embase, CNKI and Wanfang databases were examined for all relevant studies up until 8 October 2016. In all, 968 cases and 1549 controls in eight case-control studies were included which mainly consisted of Caucasian participants. The relevant data were extracted and the odds ratio (OR) with 95% confidence intervals (95% CI) calculated to assess the strength of any associations. Statistical analyses were calculated using STATA12.0 software and Revman5.3 software. The associations between SNP rs2066844, rs2066845, rs2066847, rs1861759 polymorphisms and the risk of sarcoidosis were evaluated in allelic, dominant, recessive and additive models. The pooled data showed that the rs2066845 polymorphism was associated with sarcoidosis susceptibility in allelic model (C vs. G, OR=1.86, 95% CI: 1.14-3.04, P=0.01), dominant model (GC + CC vs. GG, OR=1.84, 95% CI: 1.11-3.05, P=0.02) and additive model (GC vs. GG, OR=1.79, 95% CI: 1.08-2.97, P=0.02). However, the results suggested that the rs2066844, rs2066847 and rs1861759 polymorphisms might not be associated with a risk of sarcoidosis. This meta-analysis indicated that the 'C' allele of SNP rs2066845 may be a risk factor for sarcoidosis, especially in Caucasians, whilst rs2066844, rs2066847 and rs1861759 may not be associated with a risk of developing sarcoidosis. .
近年来,含核苷酸结合寡聚化结构域2(NOD2)基因多态性与结节病易感性之间的关联已得到广泛研究。然而,既往研究结果仍存在争议。为评估NOD2多态性与结节病易感性之间的关联,我们进行了一项荟萃分析。检索了截至2016年10月8日的PubMed、Embase、中国知网和万方数据库中的所有相关研究。总共纳入了八项病例对照研究中的968例病例和1549例对照,这些研究主要包括白种人参与者。提取相关数据并计算比值比(OR)及95%置信区间(95%CI),以评估任何关联的强度。使用STATA12.0软件和Revman5.3软件进行统计分析。在等位基因、显性、隐性和加性模型中评估了NOD2基因单核苷酸多态性(SNP)rs2066844、rs2066845、rs2066847、rs1861759多态性与结节病风险之间的关联。汇总数据显示,rs2066845多态性在等位基因模型(C与G相比,OR = 1.86,95%CI:1.14 - 3.04,P = 0.01)、显性模型(GC + CC与GG相比,OR = 1.84,95%CI:1.11 - 3.05,P = 0.02)和加性模型(GC与GG相比,OR = 1.79,95%CI:1.08 - 2.97,P = 0.02)中与结节病易感性相关。然而,结果表明rs2066844、rs2066847和rs1861759多态性可能与结节病风险无关。这项荟萃分析表明,SNP rs2066845的“C”等位基因可能是结节病的一个危险因素,尤其是在白种人中,而rs2066844、rs2066847和rs1861759可能与患结节病的风险无关。