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Variants in ABCG8 and TRAF3 genes confer risk for gallstone disease in admixed Latinos with Mapuche Native American ancestry

机译:ABCG8和TRAF3基因的变异使马普切人与美洲印第安人混血的拉丁美洲人罹患胆结石的风险

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摘要

Latin Americans and Chilean Amerindians have the highest prevalence of gallstone disease (GSD) and gallbladder cancer (GBC) in the world. A handful of loci have been associated with GSD in populations of predominantly European ancestry, however, they only explain a small portion of the genetic component of the disease. Here, we performed a genome-wide association study (GWAS) for GSD in 1,095 admixed Chilean Latinos with Mapuche Native American ancestry. Disease status was assessed by cholecystectomy or abdominal ultrasonography. Top-10 candidate variants surpassing the suggestive cutoff of P < 1 × 10−5 in the discovery cohort were genotyped in an independent replication sample composed of 1,643 individuals. Variants with positive replication were further examined in two European GSD populations and a Chilean GBC cohort. We consistently replicated the association of ABCG8 gene with GSD (rs11887534, P = 3.24 × 10−8, OR = 1.74) and identified TRAF3 (rs12882491, P = 1.11 × 10−7, OR = 1.40) as a novel candidate gene for the disease in admixed Chilean Latinos. ABCG8 and TRAF3 variants also conferred risk to GBC. Gene expression analyses indicated that TRAF3 was significantly decreased in gallbladder (P = 0.015) and duodenal mucosa (P = 0.001) of GSD individuals compared to healthy controls, where according to GTEx data in the small intestine, the presence of the risk allele contributes to the observed effect. We conclude that ABCG8 and TRAF3 genes are associated with GSD and GBC in admixed Latinos and that decreased TRAF3 levels could enhance gallbladder inflammation as is observed in GSD and GSD-associated GBC.
机译:拉丁美洲人和智利美洲印第安人是世界上胆结石疾病(GSD)和胆囊癌(GBC)患病率最高的国家。在欧洲血统为主的人群中,少数基因座与GSD相关,但是,它们仅解释了该疾病遗传成分的一小部分。在这里,我们对1095个智利拉丁裔和Mapuche美国土著血统进行了GSD的全基因组关联研究(GWAS)。通过胆囊切除术或腹部超声检查评估疾病状态。在由1643个个体组成的独立复制样本中对发现队列中超过P <1×10 -5 的建议临界值的前10个候选变体进行了基因分型。在两个欧洲GSD人群和一个智利GBC队列中进一步检查了具有阳性复制的变异体。我们一致地复制了ABCG8基因与GSD的关联(rs11887534,P = 3.24×10 -8 ,OR = 1.74),并鉴定出TRAF3(rs12882491,P = 1.11×10 −7 ,OR = 1.40)作为混合智利智利人中该疾病的新候选基因。 ABCG8和TRAF3变体也给GBC带来风险。基因表达分析表明,与健康对照组相比,GSD个体的胆囊(P = 0.015)和十二指肠黏膜(P = 0.001)的TRAF3明显降低,根据小肠中的GTEx数据,存在风险等位基因有助于观察到的效果。我们得出结论,在混合的拉丁裔中,ABCG8和TRAF3基因与GSD和GBC相关,并且降低的TRAF3水平可以增强胆囊炎症,如在GSD和GSD相关的GBC中所观察到的。

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