Facultad de Medicina, Benemérita Universidad Autónoma de Puebla, 13 Sur 2901 Col. Volcanes, C.P. 72420 Puebla, Pue, Mexico.
Laboratorio de Investigación en Fisiopatologia de Enfermedades Crónicas, Centro de Investigación Biomédica de Oriente, Instituto Mexicano del Seguro Social, Delegación Puebla, Km 4.5 Carretera Federal Atlixco-Metepec, C.P. 42730 Atlixco, Puebla, Mexico.
Reumatol Clin (Engl Ed). 2021 Oct;17(8):447-455. doi: 10.1016/j.reumae.2020.03.003.
We performed a meta-analysis to determine the effect Interleukin-6 (IL-6) promoter polymorphism (-174 G>C, -572 G>C, and -597 G>A) have on the development rheumatoid arthritis (RA) by ethnicity.
PubMed, EBSCO, LILACS, and Scopus databases were searched for studies exploring the association between any IL6 polymorphisms and RA until November 2018. Genotype distributions were extracted and, depending on the level heterogeneity, determined by the ψ-based Q test and the Inconsistency Index (I), fixed-effects or random-effects models were used to calculate pooled odds ratios (ORs) with 95% confidence intervals (95%CIs) for the heterozygous, homozygous, dominant, recessive, and allelic genetic models.
From 708 identified publications, 33 were used in this analysis. For the -174 polymorphism, Asians (OR=7.57, 95%CI: 2.28-25.14, OR=5.84, 95%CI: 2.06-16.56, OR=7.21, 95%CI: 2.30-22.63, OR=5.04, 95%CI: 1.78-14.28, OR=6.60, 95%CI: 2.26-19.28, p<.05) and Middle East countries (OR=2.30, 95%CI: 1.10-4.81, OR=2.27, 95%CI: 1.22-4.22, OR=2.29, 95%CI: 1.24-4.23, p<.05) were associated with a significant risk of developing RA. Whereas, for Latinos, the C-allele was associated with a benefit (OR=0.26, 95%CI: .08-.82, OR=.25, 95%CI: .08-.80, p<.05). For the -572 polymorphism, Asians demonstrated a significant association for the homozygous and recessive genetic models (8 studies, OR=1.56, 95%CI: 1.16-2.09, OR=1.63, 95%CI: 1.08-2.45, p<.05). For the -597 polymorphism, no association was observed.
Here, the -174 G>C polymorphism increased the risk of developing RA in Asians and Middle East populations. Interestingly, for Latinos, the polymorphism was associated with a benefit. For the -572 polymorphism, only the Asian population showed an increased risk of developing RA for the CC genotype.
我们进行了一项荟萃分析,以确定白细胞介素-6(IL-6)启动子多态性(-174 G>C、-572 G>C 和-597 G>A)在不同种族中对类风湿关节炎(RA)发病的影响。
检索了 PubMed、EBSCO、LILACS 和 Scopus 数据库,以寻找探索任何 IL6 多态性与 RA 之间关联的研究,检索时间截至 2018 年 11 月。提取基因型分布,并根据水平异质性,使用基于 ψ 的 Q 检验和不一致指数(I),采用固定效应或随机效应模型,计算杂合子、纯合子、显性、隐性和等位基因遗传模型的合并优势比(OR)及其 95%置信区间(95%CI)。
从 708 篇已识别的文献中,有 33 篇被纳入本分析。对于 -174 多态性,亚洲人(OR=7.57,95%CI:2.28-25.14,OR=5.84,95%CI:2.06-16.56,OR=7.21,95%CI:2.30-22.63,OR=5.04,95%CI:1.78-14.28,OR=6.60,95%CI:2.26-19.28,p<.05)和中东国家(OR=2.30,95%CI:1.10-4.81,OR=2.27,95%CI:1.22-4.22,OR=2.29,95%CI:1.24-4.23,p<.05)与发生 RA 的显著风险相关。而对于拉丁裔人,C 等位基因与益处相关(OR=0.26,95%CI:.08-.82,OR=.25,95%CI:.08-.80,p<.05)。对于 -572 多态性,亚洲人在同型和隐性遗传模型中表现出显著的相关性(8 项研究,OR=1.56,95%CI:1.16-2.09,OR=1.63,95%CI:1.08-2.45,p<.05)。对于 -597 多态性,未观察到相关性。
本研究中,-174 G>C 多态性增加了亚洲人和中东人群发生 RA 的风险。有趣的是,对于拉丁裔人,该多态性与益处相关。对于 -572 多态性,只有亚洲人群的 CC 基因型显示出发生 RA 的风险增加。