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肥胖与代谢异常中的肠道微生物群:与组成或功能有关?

Gut Microbiota in Obesity and Metabolic Abnormalities: A Matter of Composition or Functionality?

机构信息

Consejo Nacional de Ciencia y Tecnología (CONACYT), Ciudad de México, México; Unidad de Genómica de Poblaciones Aplicada a la Salud, Facultad de Química, UNAM/Instituto Nacional de Medicina Genómica, Ciudad de México, México.

Unidad de Genómica de Poblaciones Aplicada a la Salud, Facultad de Química, UNAM/Instituto Nacional de Medicina Genómica, Ciudad de México, México.

出版信息

Arch Med Res. 2017 Nov;48(8):735-753. doi: 10.1016/j.arcmed.2017.11.003. Epub 2017 Dec 29.

Abstract

The obesity pandemic and the metabolic complications derived from it represent a major public health challenge worldwide. Although obesity is a multifactorial disease, research from the past decade suggests that the gut microbiota interacts with host genetics and diet, as well as with other environmental factors, and thus contributes to the development of obesity and related complications. Despite abundant research on animal models, substantial evidence from humans has only started to accumulate over the past few years. Thus, the aim of the present review is to discuss structural and functional characteristics of the gut microbiome in human obesity, challenges associated with multi-omic technologies, and advances in identifying microbial metabolites with a direct link to obesity and metabolic complications. To date, studies suggests that obesity is related to low microbial diversity and taxon depletion sometimes resulting from an interaction with host dietary habits and genotype. These findings support the idea that the depletion or absence of certain taxa leaves an empty niche, likely leading to compromised functionality and thus promoting dysbiosis. Although the role of altered gut microbiota as cause or consequence of obesity remains controversial, research on microbial genomes and metabolites points towards an increased extraction of energy from the diet in obesity and suggests that metabolites, such as trimethylamine-N-oxide or branched-chain amino acids, participate in metabolic complications. Future research should be focused on structural and functional levels to unravel the mechanism linking gut microbiota and obesity.

摘要

肥胖症大流行及其带来的代谢并发症是全球主要的公共卫生挑战。尽管肥胖是一种多因素疾病,但过去十年的研究表明,肠道微生物群与宿主遗传和饮食以及其他环境因素相互作用,从而导致肥胖及其相关并发症的发生。尽管在动物模型方面进行了大量研究,但近年来才开始积累大量来自人类的证据。因此,本综述的目的是讨论人类肥胖症中肠道微生物组的结构和功能特征、与多组学技术相关的挑战,以及识别与肥胖和代谢并发症直接相关的微生物代谢产物方面的进展。迄今为止的研究表明,肥胖与微生物多样性降低和分类群耗竭有关,这可能是由于与宿主饮食习惯和基因型相互作用所致。这些发现支持了这样一种观点,即某些分类群的耗竭或缺失会留下一个空的生态位,可能导致功能受损,从而促进了微生态失调。尽管肠道微生物群的改变是肥胖的原因还是后果仍存在争议,但对微生物基因组和代谢产物的研究表明,肥胖症从饮食中提取能量的能力增加,并表明代谢产物(如三甲胺 N-氧化物或支链氨基酸)参与代谢并发症的发生。未来的研究应集中在结构和功能水平上,以揭示肠道微生物群与肥胖之间的联系机制。

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