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首页> 外文期刊>American Journal of Epidemiology >Association of Type 2 Diabetes Susceptibility Variants With Advanced Prostate Cancer Risk in the Breast and Prostate Cancer Cohort Consortium
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Association of Type 2 Diabetes Susceptibility Variants With Advanced Prostate Cancer Risk in the Breast and Prostate Cancer Cohort Consortium

机译:2型糖尿病易感性变异与乳腺癌和前列腺癌研究组中晚期前列腺癌风险的相关性

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Observational studies have found an inverse association between type 2 diabetes (T2D) and prostate cancer (PCa), and genome-wide association studies have found common variants near 3 loci associated with both diseases. The authors examined whether a genetic background that favors T2D is associated with risk of advanced PCa. Data from the National Cancer Institute's Breast and Prostate Cancer Cohort Consortium, a genome-wide association study of 2,782 advanced PCa cases and 4,458 controls, were used to evaluate whether individual single nucleotide polymorphisms or aggregations of these 36 T2D susceptibility loci are associated with PCa. Ten T2D markers near 9 loci (NOTCH2, ADCY5, JAZF1, CDKN2A/B, TCF7L2, KCNQ1, MTNR1B, FTO, and HNF1B) were nominally associated with PCa (P 0.05); the association for single nucleotide polymorphism rs757210 at the HNF1B locus was significant when multiple comparisons were accounted for (adjusted P = 0.001). Genetic risk scores weighted by the T2D log odds ratio and multilocus kernel tests also indicated a significant relation between T2D variants and PCa risk. A mediation analysis of 9,065 PCa cases and 9,526 controls failed to produce evidence that diabetes mediates the association of the HNF1B locus with PCa risk. These data suggest a shared genetic component between T2D and PCa and add to the evidence for an interrelation between these diseases.
机译:观察性研究发现2型糖尿病(T2D)和前列腺癌(PCa)之间存在负相关,而全基因组关联研究发现了与这两种疾病相关的3个基因座附近的常见变异。作者检查了有利于T2D的遗传背景是否与晚期PCa风险相关。来自美国国家癌症研究所的乳腺癌和前列腺癌研究小组的数据是一项对2,782例晚期PCa病例和4,458例对照的全基因组关联研究,用于评估这36个T2D易感性基因座的单个单核苷酸多态性或聚集体是否与PCa相关。在9个基因座附近的十个T2D标记(NOTCH2,ADCY5,JAZF1,CDKN2A / B,TCF7L2,KCNQ1,MTNR1B,FTO和HNF1B)与PCa相关联(P <0.05);当考虑多个比较时,HNF1B位点的单核苷酸多态性rs757210的关联很显着(调整后的P = 0.001)。由T2D对数比值比和多基因座核试验加权的遗传风险评分也表明T2D变异体与PCa风险之间存在显着关系。对9,065例PCa病例和9,526例对照进行的调解分析未能提供证据证明糖尿病介导了HNF1B基因座与PCa风险的关联。这些数据表明T2D和PCa之间存在共同的遗传成分,并为这些疾病之间的相互关系提供了证据。

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