Center for Data Sciences, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Division of Genetics, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Nat Genet. 2022 Nov;54(11):1640-1651. doi: 10.1038/s41588-022-01213-w. Epub 2022 Nov 4.
Rheumatoid arthritis (RA) is a highly heritable complex disease with unknown etiology. Multi-ancestry genetic research of RA promises to improve power to detect genetic signals, fine-mapping resolution and performances of polygenic risk scores (PRS). Here, we present a large-scale genome-wide association study (GWAS) of RA, which includes 276,020 samples from five ancestral groups. We conducted a multi-ancestry meta-analysis and identified 124 loci (P < 5 × 10), of which 34 are novel. Candidate genes at the novel loci suggest essential roles of the immune system (for example, TNIP2 and TNFRSF11A) and joint tissues (for example, WISP1) in RA etiology. Multi-ancestry fine-mapping identified putatively causal variants with biological insights (for example, LEF1). Moreover, PRS based on multi-ancestry GWAS outperformed PRS based on single-ancestry GWAS and had comparable performance between populations of European and East Asian ancestries. Our study provides several insights into the etiology of RA and improves the genetic predictability of RA.
类风湿性关节炎(RA)是一种高度遗传的复杂疾病,其病因未知。RA 的多祖先进化遗传学研究有望提高检测遗传信号的能力、精细定位分辨率和多基因风险评分(PRS)的性能。在这里,我们进行了一项大规模的 RA 全基因组关联研究(GWAS),该研究包括来自五个祖先进化群体的 276,020 个样本。我们进行了多祖先进化荟萃分析,确定了 124 个位点(P < 5 × 10),其中 34 个是新的。新发现的位点的候选基因表明免疫系统(例如 TNIP2 和 TNFRSF11A)和关节组织(例如 WISP1)在 RA 发病机制中起着重要作用。多祖先进化精细定位确定了具有生物学意义的潜在因果变异(例如 LEF1)。此外,基于多祖先进化 GWAS 的 PRS 优于基于单祖先进化 GWAS 的 PRS,并且在欧洲和东亚祖先进化的人群中具有可比的性能。我们的研究为 RA 的发病机制提供了一些新的见解,并提高了 RA 的遗传可预测性。