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Genes identified in Asian SLE GWASs are also associated with SLE in Caucasian populations

机译:在亚洲SLE GWAS中鉴定的基因也与高加索人群的SLE相关

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Recent genome-wide association studies (GWASs) conducted in Asian populations have identified novel risk loci for systemic lupus erythematosus (SLE). Here, we genotyped 10 single-nucleotide polymorphisms (SNPs) in eight such loci and investigated their disease associations in three independent Caucasian SLE case-control cohorts recruited from Sweden, Finland and the United States. The disease associations of the SNPs in ETS1, IKZF1, LRRC18-WDFY4, RASGRP3, SLC15A4, TNIP1 and 16p11.2 were replicated, whereas no solid evidence of association was observed for the 7q11.23 locus in the Caucasian cohorts. SLC15A4 was significantly associated with renal involvement in SLE. The association of TNIP1 was more pronounced in SLE patients with renal and immunological disorder, which is corroborated by two previous studies in Asian cohorts. The effects of all the associated SNPs, either conferring risk for or being protective against SLE, were in the same direction in Caucasians and Asians. The magnitudes of the allelic effects for most of the SNPs were also comparable across different ethnic groups. On the contrary, remarkable differences in allele frequencies between Caucasian and Asian populations were observed for all associated SNPs. In conclusion, most of the novel SLE risk loci identified by GWASs in Asian populations were also associated with SLE in Caucasian populations. We observed both similarities and differences with respect to the effect sizes and risk allele frequencies across ethnicities.
机译:最近在亚洲人群中进行的全基因组关联研究(GWAS)已确定系统性红斑狼疮(SLE)的新型风险基因座。在这里,我们对八个这样的基因座中的10个单核苷酸多态性(SNP)进行了基因分型,并在瑞典,芬兰和美国招募的三个独立的白种人SLE病例对照队列中研究了它们的疾病关联。复制了ETS1,IKZF1,LRRC18-WDFY4,RASGRP3,SLC15A4,TNIP1和16p11.2中SNP的疾病关联,而在白种人队列中未观察到7q11.23关联的确凿证据。 SLC15A4与肾脏参与SLE显着相关。 TNIP1的相关性在患有肾脏和免疫系统疾病的SLE患者中更为明显,这在亚洲的两项先前研究中得到了证实。高加索人和亚洲人中,所有相关SNPs的作用都朝着相同的方向发展,无论这些风险赋予SLE风险还是对SLE起到防护作用。大多数SNP的等位基因效应的大小在不同种族之间也相当。相反,对于所有相关的SNP,在白种人和亚洲人群之间观察到等位基因频率的显着差异。总之,在亚洲人群中,GWAS鉴定出的大多数新型SLE风险基因位点也与白种人人群中的SLE相关。我们观察到跨种族的影响大小和风险等位基因频率的相似性和差异。

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