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Common shared genetic variation behind decreased risk of breast cancer in celiac disease

机译:乳糜泻乳腺癌风险降低背后的共同共有遗传变异

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摘要

There is epidemiologic evidence showing that women with celiac disease have reduced risk of later developing breast cancer, however, the etiology of this association is unclear. Here, we assess the extent of genetic overlap between the two diseases. Through analyses of summary statistics on densely genotyped immunogenic regions, we show a significant genetic correlation (r = −0.17, s.e. 0.05, P < 0.001) and overlap (P permuted < 0.001) between celiac disease and breast cancer. Using individual-level genotype data from a Swedish cohort, we find higher genetic susceptibility to celiac disease summarized by polygenic risk scores to be associated with lower breast cancer risk (ORper-SD, 0.94, 95% CI 0.91 to 0.98). Common single nucleotide polymorphisms between the two diseases, with low P-values (P CD < 1.00E-05, P BC ≤ 0.05), mapped onto genes enriched for immunoregulatory and apoptotic processes. Our results suggest that the link between breast cancer and celiac disease is due to a shared polygenic variation of immune related regions, uncovering pathways which might be important for their development.
机译:流行病学证据表明,患有腹腔疾病的妇女降低了以后患乳腺癌的风险,但是,这种关联的病因尚不清楚。在这里,我们评估了两种疾病之间的遗传重叠程度。通过对致密基因型免疫原性区域的汇总统计分析,我们发现腹腔疾病与乳腺癌之间存在显着的遗传相关性(r = −0.17,s.e。0.05,P <0.001)和重叠(P permuted <0.001)。使用来自瑞典队列的个体水平基因型数据,我们发现对乳糜泻的较高遗传易感性(通过多基因风险评分总结)与较低的乳腺癌风险相关(ORper-SD,0.94、95%CI 0.91至0.98)。两种疾病之间的常见单核苷酸多态性具有较低的P值(P CD <1.00E-05,P BC≤0.05),并定位于丰富的免疫调节和凋亡过程基因上。我们的研究结果表明,乳腺癌和腹腔疾病之间的联系是由于免疫相关区域的多基因变异所致,揭示了可能对其发展至关重要的途径。

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