Massachusetts General Hospital, Harvard Medical School, Boston, Massachusetts, and Broad Institute, Cambridge, Massachusetts.
Broad Institute, Cambridge, Massachusetts, and Merck Research Laboratories and Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.
Arthritis Rheumatol. 2017 May;69(5):976-985. doi: 10.1002/art.40051. Epub 2017 Mar 31.
Genetic factors underlying susceptibility to rheumatoid arthritis (RA) in Arab populations are largely unknown. This genome-wide association study (GWAS) was undertaken to explore the generalizability of previously reported RA loci to Arab subjects and to discover new Arab-specific genetic loci.
The Genetics of Rheumatoid Arthritis in Some Arab States Study was designed to examine the genetics and clinical features of RA patients from Jordan, the Kingdom of Saudi Arabia, Lebanon, Qatar, and the United Arab Emirates. In total, >7 million single-nucleotide polymorphisms (SNPs) were tested for association with RA overall and with seropositive or seronegative RA in 511 RA cases and 352 healthy controls. In addition, replication of 15 signals was attempted in 283 RA cases and 221 healthy controls. A genetic risk score of 68 known RA SNPs was also examined in this study population.
Three loci (HLA region, intergenic 5q13, and 17p13 at SMTNL2/GGT6) reached genome-wide significance in the analyses of association with RA and with seropositive RA, and for all 3 loci, evidence of independent replication was demonstrated. Consistent with the findings in European and East Asian populations, the association of RA with HLA-DRB1 amino acid position 11 conferred the strongest effect (P = 4.8 × 10 ), and a weighted genetic risk score of previously associated RA loci was found to be associated with RA (P = 3.41 × 10 ) and with seropositive RA (P = 1.48 × 10 ) in this population. In addition, 2 novel associations specific to Arab populations were found at the 5q13 and 17p13 loci.
This first RA GWAS in Arab populations confirms that established HLA-region and known RA risk alleles contribute strongly to the risk and severity of disease in some Arab groups, suggesting that the genetic architecture of RA is similar across ethnic groups. Moreover, this study identified 2 novel RA risk loci in Arabs, offering further population-specific insights into the pathophysiology of RA.
阿拉伯人群患类风湿关节炎(RA)的遗传易感性的相关基因尚不清楚。本全基因组关联研究(GWAS)旨在探讨先前报道的 RA 易感基因座在阿拉伯人群中的普遍性,并发现新的阿拉伯人群特有的遗传基因座。
“某些阿拉伯国家的类风湿关节炎遗传学研究”旨在研究来自约旦、沙特阿拉伯王国、黎巴嫩、卡塔尔和阿拉伯联合酋长国的 RA 患者的遗传学和临床特征。共有超过 700 万个单核苷酸多态性(SNP)用于与 RA 进行整体关联分析,以及与血清阳性或血清阴性 RA 进行关联分析,共纳入 511 例 RA 病例和 352 例健康对照。此外,还在 283 例 RA 病例和 221 例健康对照中尝试了 15 个信号的复制。在该研究人群中还检查了 68 个已知 RA SNP 的遗传风险评分。
在与 RA 和血清阳性 RA 的关联分析中,3 个基因座(HLA 区域、5q13 基因间区和 17p13 上的 SMTNL2/GGT6)达到了全基因组显著性水平,所有 3 个基因座均显示出独立复制的证据。与欧洲和东亚人群的研究结果一致,RA 与 HLA-DRB1 氨基酸位置 11 的关联赋予了最强的效应(P=4.8×10-8),先前与 RA 相关的基因座的加权遗传风险评分与 RA(P=3.41×10-8)和血清阳性 RA(P=1.48×10-8)相关。此外,在 5q13 和 17p13 基因座还发现了 2 个特定于阿拉伯人群的新关联。
这是首次在阿拉伯人群中进行的 RA GWAS,证实了已建立的 HLA 区域和已知的 RA 风险等位基因在一些阿拉伯群体中对疾病的风险和严重程度有很强的影响,这表明 RA 的遗传结构在不同种族群体中是相似的。此外,本研究在阿拉伯人群中发现了 2 个新的 RA 风险基因座,为 RA 的病理生理学提供了进一步的人群特异性见解。