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与超重和肥胖男性组织特异性胰岛素敏感性相关的个体和队列特异性肠道微生物群模式。

Individual and cohort-specific gut microbiota patterns associated with tissue-specific insulin sensitivity in overweight and obese males.

机构信息

Laboratory of Microbiology, Wageningen University & Research, 6708 WE, Wageningen, The Netherlands.

TI Food and Nutrition (TIFN), P.O. Box 557, 6700 AN, Wageningen, The Netherlands.

出版信息

Sci Rep. 2020 May 5;10(1):7523. doi: 10.1038/s41598-020-64574-4.

Abstract

A growing body of evidence suggests that the human gut microbiota plays a role in the development of obesity and related metabolic diseases. However, there is little consensus between studies, which could be due to biological as well as technical variation. In addition, little human data are available to investigate whether tissue-specific insulin sensitivity is related to specific microbial patterns. We examined this relation in two independent cohorts of overweight and obese pre-diabetic men, using phylogenetic microarray data and hepatic, peripheral and adipose tissue insulin sensitivity that were determined by a two-step hyperinsulinemic-euglycemic clamp with [6,6-H]-glucose tracer infusion. Despite a prominent subject-specific microbiota, we found significant associations of microbial taxa with tissue-specific insulin sensitivity using regression analysis. Using random forests we found moderate associations with other measures of glucose homeostasis in only one of the cohorts (fasting glucose concentrations AUC = 0.66 and HbA AUC = 0.65). However, all findings were cohort-specific due to pronounced variation in microbiota between cohorts, suggesting the existence of alternative states for dysbiosis in metabolic syndrome patients. Our findings suggest individual or group related dynamics, instead of universal microbiota signals, related to the host when the overweight or obese state has already developed and argue that care should be taken with extrapolating significant correlations from single cohorts, into generalized biological relevance.

摘要

越来越多的证据表明,人类肠道微生物群在肥胖和相关代谢性疾病的发展中起作用。然而,研究之间几乎没有共识,这可能是由于生物学和技术上的差异。此外,几乎没有人类数据可用于研究组织特异性胰岛素敏感性是否与特定的微生物模式有关。我们使用系统发育微阵列数据和通过两步高胰岛素-正常血糖钳夹联合 [6,6-H]-葡萄糖示踪剂输注来确定的肝、外周和脂肪组织胰岛素敏感性,在两个独立的超重和肥胖前驱糖尿病男性队列中检查了这种关系。尽管存在明显的个体特异性微生物群,但我们使用回归分析发现微生物类群与组织特异性胰岛素敏感性之间存在显著关联。使用随机森林,我们仅在一个队列中发现了与其他血糖稳态测量值的中度关联(AUC 为 0.66 的空腹血糖浓度和 AUC 为 0.65 的 HbA)。然而,由于队列之间微生物群存在明显差异,所有发现都是队列特异性的,这表明代谢综合征患者的肠道菌群失调可能存在替代状态。我们的研究结果表明,当超重或肥胖状态已经发展时,与宿主相关的是个体或群体相关的动态,而不是普遍的微生物信号,并认为从单个队列推断具有统计学意义的相关性时,应格外注意将其推广到更广泛的生物学相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fcf5/7200728/599e1005f817/41598_2020_64574_Fig1_HTML.jpg

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