首页> 外文期刊>Journal of clinical biochemistry and nutrition. >Prediction of functional profiles of gut microbiota from 16S rRNA metagenomic data provides a more robust evaluation of gut dysbiosis occurring in Japanese type 2 diabetic patients
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Prediction of functional profiles of gut microbiota from 16S rRNA metagenomic data provides a more robust evaluation of gut dysbiosis occurring in Japanese type 2 diabetic patients

机译:根据16S rRNA宏基因组学数据预测肠道菌群的功能谱,可对日本2型糖尿病患者发生的肠道营养不良进行更可靠的评估

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We assessed whether gut microbial functional profiles predicted from 16S rRNA metagenomics differed in Japanese type 2 diabetic patients. A total of 22 Japanese subjects were recruited from our outpatient clinic in an observational study. Fecal samples were obtained from 12 control and 10 type 2 diabetic subjects. 16S rRNA metagenomic data were generated and functional profiles predicted using “Phylogenetic Investigation of Communities by Reconstruction of Unobserved States” software. We measured the parameters of glucose metabolism, gut bacterial taxonomy and functional profile, and examined the associations in a cross-sectional manner. Eleven of 288 “Kyoto Encyclopedia of Genes and Genomes” pathways were significantly enriched in diabetic patients compared with control subjects ( p Insulin signaling pathway and Glycolysis/Gluconeogenesis , showed strong, positive correlations with hemoglobin A1c (HbA1c) and fasting plasma glucose (FPG) levels. Bacterial taxonomic analysis showed that genus Blautia significantly differed between groups and had negative correlations with HbA1c and FPG levels. Our findings suggest a novel pathophysiological relationship between gut microbial communities and diabetes, further highlighting the significance and utility of combining prediction of functional profiles with ordinal bacterial taxonomic analysis (UMIN Clinical Trails Registry number: UMIN000026592).
机译:我们评估了在日本2型糖尿病患者中,从16S rRNA宏基因组学预测的肠道微生物功能谱是否有所不同。在一项观察性研究中,我们的门诊共招募了22名日本受试者。从12名对照和10名2型糖尿病受试者获得粪便样品。生成了16S rRNA宏基因组学数据,并使用“通过重建观察不到的国家对社区进行系统发育调查”软件预测了功能概况。我们测量了葡萄糖代谢,肠道细菌分类学和功能概况的参数,并以截面的方式检查了这些关联。与对照组相比,糖尿病患者的288个“基因和基因组京都百科全书”途径中有11个途径显着丰富(p胰岛素信号传导途径和糖酵解/糖异生,与血红蛋白A 1c (HbA 1c )和空腹血糖(FPG)水平。细菌分类学分析显示,布鲁氏菌属之间存在显着差异,并且与HbA 1c 和FPG水平呈负相关。肠道微生物群落与糖尿病之间的新型病理生理关系,进一步凸显了将功能概况与序贯细菌分类学分析相结合的重要性和实用性(UMIN Clinical Trails注册号:UMIN000026592)。

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