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首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >Sterol transporter adenosine triphosphate-binding cassette transporter G8, gallstones, and biliary cancer in 62,000 individuals from the general population.
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Sterol transporter adenosine triphosphate-binding cassette transporter G8, gallstones, and biliary cancer in 62,000 individuals from the general population.

机译:甾族转运蛋白三磷酸腺苷结合盒转运蛋白G8,胆结石和胆道癌在普通人群中有62,000人。

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摘要

Gallstone disease, a risk factor for biliary cancer, has a strong heritable component, but the underlying genes are largely unknown. To test the hypothesis that ABCG8 (adenosine triphosphate-binding cassette transporter G8) Asp19His (D19H) genotype predicted risk of gallstones and biliary cancer in the general population, we studied 62,279 white individuals from The Copenhagen City Heart Study and The Copenhagen General Population Study, randomly selected to reflect the adult Danish population aged 20 to 80+ years. Endpoints were recorded from January 1976 through May 2009. During a mean follow-up of, respectively, 31 and 4.4 years, 3124 participants developed symptomatic gallstone disease and 30 developed biliary cancer. The multifactorially adjusted hazard ratio for symptomatic gallstone disease was 1.9 (95% confidence interval, 1.7-2.1) in DH heterozygotes (prevalence, 12%), and 3.3 (2.3-4.6) in HH homozygotes (0.4%) versus noncarriers (P for trend <0.001). Mean age at onset of symptomatic gallstone disease was 56 years for noncarriers, 54 for DH heterozygotes, and 52 for HH homozygotes (P for trend <0.001). The fraction of all gallstones attributed to D19H was 11%. The multifactorially adjusted hazard ratio for biliary cancer was 4.0 (1.9-8.4) in DH heterozygotes and HH homozygotes combined versus noncarriers (P < 0.001). The fraction of all biliary cancers attributed to the D19H genotype was 27%. Finally, D19H genotype associated with stepwise increases in plasma levels of alanine aminotransferase and gamma glutamyltransferase of up to 14% and 25% in HH homozygotes, and with corresponding stepwise reductions in plasma levels of total and low-density lipoprotein cholesterol of up to 5% versus noncarriers (all comparisons, P for trend <0.001). CONCLUSION: In this general population cohort, ABCG8 D19H genotype was an important predictor of both symptomatic gallstone disease and biliary cancer.
机译:胆石病是胆道癌的危险因素,具有很强的遗传性,但其潜在基因在很大程度上尚不清楚。为了验证ABCG8(三磷酸腺苷结合盒转运体G8)Asp19His(D19H)基因型预测普通人群胆结石和胆道癌风险的假设,我们研究了来自哥本哈根市心脏研究和哥本哈根总人口研究的62,279名白人,随机选择以反映20至80岁以上的丹麦成年人口。记录了从1976年1月到2009年5月的终点。在平均31年和4.4年的平均随访期间,有3124名参与者发展为有症状的胆结石病,而30名则发展为胆道癌。与非携带者相比,DH杂合子(患病率,12%)中有症状胆结石病的多因素调整风险比为1.9(95%置信区间,1.7-2.1),HH纯合子(0.4%)中为3.3(2.3-4.6)。趋势<0.001)。有症状胆结石病发作的平均年龄为非携带者为56岁,DH杂合子为54岁,HH纯合子为52岁(趋势<0.001)。归因于D19H的所有胆结石比例为11%。 DH杂合子和HH纯合子与非携带者合用时,经多因素调整的胆道癌危险比为4.0(1.9-8.4)(P <0.001)。在所有归因于D19H基因型的胆道癌中,占27%。最后,D19H基因型与HH纯合子的血浆丙氨酸转氨酶和γ-谷氨酰转移酶的血浆水平逐步升高有关,分别高达14%和25%,并且血浆中总和低密​​度脂蛋白胆固醇的血浆水平也相应降低,最高可达5%与非运营商相比(所有比较,趋势P均<0.001)。结论:在这个一般人群中,ABCG8 D19H基因型是有症状胆结石疾病和胆道癌的重要预测指标。

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