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通过免疫芯片荟萃分析策略分析巨细胞血管炎的常见遗传成分。

Analysis of the common genetic component of large-vessel vasculitides through a meta-Immunochip strategy.

机构信息

Instituto de Parasitología y Biomedicina 'López-Neyra', IPBLN-CSIC, PTS Granada, Granada, Spain.

Departamento de Genética e Instituto de Biotecnología, Universidad de Granada, Granada 18016, Spain.

出版信息

Sci Rep. 2017 Mar 9;7:43953. doi: 10.1038/srep43953.

Abstract

Giant cell arteritis (GCA) and Takayasu's arteritis (TAK) are major forms of large-vessel vasculitis (LVV) that share clinical features. To evaluate their genetic similarities, we analysed Immunochip genotyping data from 1,434 LVV patients and 3,814 unaffected controls. Genetic pleiotropy was also estimated. The HLA region harboured the main disease-specific associations. GCA was mostly associated with class II genes (HLA-DRB1/HLA-DQA1) whereas TAK was mostly associated with class I genes (HLA-B/MICA). Both the statistical significance and effect size of the HLA signals were considerably reduced in the cross-disease meta-analysis in comparison with the analysis of GCA and TAK separately. Consequently, no significant genetic correlation between these two diseases was observed when HLA variants were tested. Outside the HLA region, only one polymorphism located nearby the IL12B gene surpassed the study-wide significance threshold in the meta-analysis of the discovery datasets (rs755374, P = 7.54E-07; OR = 1.19, OR = 1.50). This marker was confirmed as novel GCA risk factor using four additional cohorts (P = 5.52E-04, OR = 1.16). Taken together, our results provide evidence of strong genetic differences between GCA and TAK in the HLA. Outside this region, common susceptibility factors were suggested, especially within the IL12B locus.

摘要

巨细胞动脉炎(GCA)和 Takayasu 动脉炎(TAK)是大血管血管炎(LVV)的主要形式,它们具有共同的临床特征。为了评估它们的遗传相似性,我们分析了 1434 名 LVV 患者和 3814 名未受影响的对照者的 Immunochip 基因分型数据。还估计了遗传多效性。HLA 区域包含主要的疾病特异性关联。GCA 主要与 II 类基因(HLA-DRB1/HLA-DQA1)相关,而 TAK 主要与 I 类基因(HLA-B/MICA)相关。与 GCA 和 TAK 分别分析相比,在跨疾病荟萃分析中,HLA 信号的统计学意义和效应大小都大大降低。因此,当测试 HLA 变体时,未观察到这两种疾病之间存在显著的遗传相关性。除 HLA 区域外,在发现数据集的荟萃分析中,仅位于 IL12B 基因附近的一个多态性超过了全基因组显著性阈值(rs755374,P=7.54E-07;OR=1.19,OR=1.50)。使用另外四个队列证实了该标记物是新的 GCA 风险因素(P=5.52E-04,OR=1.16)。总之,我们的结果提供了 GCA 和 TAK 在 HLA 中存在强烈遗传差异的证据。在该区域之外,还提出了常见的易感因素,尤其是在 IL12B 基因座内。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d43/5344032/faea7cdad3dc/srep43953-f1.jpg

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