Facultad de Ciencias de la Salud, Universidad Autónoma de Chile, Talca, Chile.
Inmunología, Centro de Investigaciones Biomédicas (CINBIO), Universidad de Vigo, Vigo, Spain.
Sci Rep. 2020 May 12;10(1):7879. doi: 10.1038/s41598-020-64659-0.
Large genome-wide association studies (GWAS) have increased our knowledge of the genetic risk factors of rheumatoid arthritis (RA). However, little is known about genetic susceptibility in populations with a large admixture of Amerindian ancestry. The aim of the present study was to test the generalizability of previously reported RA loci in a Latin American (LA) population with admixed ancestry. We selected 128 single nucleotide polymorphisms (SNPs) in linkage equilibrium, with high association to RA in multiple populations of non-Amerindian origin. Genotyping of 118 SNPs was performed in 313 RA patients/487 healthy control subjects by mid-density arrays of polymerase chain reaction (PCR). Some of the identified associations were validated in an additional cohort (250 cases/290 controls). One marker, the SNP rs2451258, located upstream of T Cell Activation RhoGTPase Activating Protein (TAGAP) gene, showed significant association with RA (p = 5 × 10), whereas 18 markers exhibited suggestive associations (p < 0.05). Haplotype testing showed association of some groups of adjacent SNPs around the signal transducer and activator of transcription 4 (STAT4) gene (p = 9.82 × 10 to 2.04 × 10) with RA. Our major finding was little replication of previously reported genetic associations with RA. These results suggest that performing GWAS and admixture mapping in LA populations has the potential to reveal novel loci associated with RA. This in turn might help to gain insight into the 'pathogenomics' of this disease and to explore trans-population differences for RA in general.
大型全基因组关联研究(GWAS)增加了我们对类风湿关节炎(RA)遗传风险因素的了解。然而,对于具有大量美洲印第安人血统混合的人群中的遗传易感性知之甚少。本研究的目的是在具有混合血统的拉丁美洲(LA)人群中检验先前报道的 RA 基因座的普遍性。我们选择了 128 个处于连锁平衡状态的单核苷酸多态性(SNP),这些 SNP 与非美洲印第安起源的多个人群中的 RA 具有高度关联。通过聚合酶链反应(PCR)的中密度阵列对 313 名 RA 患者/487 名健康对照者的 118 个 SNP 进行基因分型。在另外一个队列(250 例病例/290 例对照)中验证了一些已确定的关联。一个标记物,即位于 T 细胞激活 Rho GTPase 激活蛋白(TAGAP)基因上游的 SNP rs2451258,与 RA 显著相关(p=5×10),而 18 个标记物表现出提示性关联(p<0.05)。单体型测试显示,信号转导和转录激活因子 4(STAT4)基因周围一些相邻 SNP 组的关联(p=9.82×10 至 2.04×10)与 RA 相关。我们的主要发现是先前报道的与 RA 相关的遗传关联复制较少。这些结果表明,在 LA 人群中进行 GWAS 和混合制图有可能揭示与 RA 相关的新基因座。这反过来又有助于深入了解该疾病的“病原体组学”,并探索 RA 一般的跨人群差异。