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Human genetic determinants of the gut microbiome and their associations with health and disease: a phenome-wide association study

机译:肠道微生物组的人类遗传决定因素及其与健康疾病的关联:苯甲酸纤维协会研究

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Small-scale studies have suggested a link between the human gut microbiome and highly prevalent diseases. However, the extent to which the human gut microbiome can be considered a determinant of disease and healthy aging remains unknown. We aimed to determine the spectrum of diseases that are linked to the human gut microbiome through the utilization of its genetic determinants as a proxy for its composition. 180 single nucleotide polymorphisms (SNPs) known to influence the human gut microbiome were used to assess the association with health and disease outcomes in 422,417 UK Biobank participants. Potential causal estimates were obtained using a Mendelian randomization (MR) approach. From the total sample analysed (mean age was 57?±?8?years), 194,567 (46%) subjects were male. Median exposure was 66-person years (interquartile range 59–72). Eleven SNPs were significantly associated with 28 outcomes (Bonferroni corrected P value??4.63·10?6) including food intake, hypertension, atopy, COPD, BMI, and lipids. Multiple SNP MR pointed to a possible causal link between Ruminococcus flavefaciens and hypertension, and Clostridium and platelet count. Microbiota and their metabolites might be of importance in the interplay between overlapping pathophysiological processes, although challenges remain in establishing causal relationships.
机译:小型研究表明人体肠道微生物组和高度普遍性的疾病之间的联系。然而,人体肠道微生物组可以被认为是疾病和健康老化的决定因素的程度仍然未知。我们旨在通过利用其遗传决定因素作为其组成的代理来确定与人体肠道微生物组合的疾病的光谱。已知影响人体肠道微生物组的单核苷酸多态性(SNP)用于评估422,417英国Biobank参与者的健康和疾病结果的关联。使用孟德尔随机化(MR)方法获得潜在的因果估计。从分析的总样本(平均年龄为57?±8?岁),194,567(46%)是男性。中位数暴露为66人(第59-72级)。 11个SNP与28个结果显着相关(Bonferroni校正的P值?<?4.63·10?6),包括食物摄入,高血压,土木,COPD,BMI和脂质。多个SNP MR指向喇菇之间的可能因果关系,钻头球菌和高血压和梭菌和血小板计数。 Microbiota及其代谢物在重叠的病理生理过程之间的相互作用中可能具有重要性,尽管仍然存在建立因果关系。

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