间歇性禁食以表型依赖的方式调节人体肠道微生物群多样性:系统综述。

IF 2.5 Q3 MICROBIOLOGY
Bioscience of microbiota, food and health Pub Date : 2024-01-01 Epub Date: 2024-04-29 DOI:10.12938/bmfh.2023-111
Adriyan Pramono, Martha Ardiaria, Edward Kurnia Setiawan Limijadi, Etika Ratna Noer, Endang Sri Lestari, Ferbian Milas Siswanto
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引用次数: 0

摘要

累积的证据表明,间歇性禁食(IF)对人体代谢健康有益。有研究表明,间歇性禁食对肠道微生物群的影响可能会介导这些有益作用。因此,我们假设间歇性禁食可能会影响人体肠道微生物群。根据系统综述和元分析首选报告项目(PRISMA)协议,我们使用 PubMed、Scopus 和 CINAHL 数据库进行了系统综述。我们在 PROSPERO 注册了我们的系统综述协议,注册号为 CRD42021270050。我们纳入了截至 2023 年 4 月 30 日发表的人类干预研究。我们使用美国国立卫生研究院(NIH)干预研究质量评估工具对纳入研究的质量进行了评估。在数据库中搜索出 166 项研究,其中 13 项符合最终定性分析的所有标准。大量证据表明,IF 可调节瘦人(相对健康)和相对健康的超重/肥胖者的人体肠道微生物群 alpha 和 beta 多样性,但不会调节代谢综合征患者的人体肠道微生物群 alpha 和 beta 多样性。此外,IF 还能改变所有表型的人类肠道微生物群组成。值得关注的是,中频干预后的肠道微生物群分类群或微生物代谢物与代谢指标相关。根据这篇综述,IF 会影响人体肠道微生物群的多样性和分类水平。个体代谢表型可能会改变 IF 对肠道微生物群多样性和分类水平的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Intermittent fasting modulates human gut microbiota diversity in a phenotype-dependent manner: a systematic review.

Cumulative evidence suggests that intermittent fasting (IF) has beneficial effects on human metabolic health. It has been indicated that its impact on the gut microbiota may mediate these beneficial effects. As a result, we hypothesized that IF may impact the human gut microbiota. A systematic review was carried out according to the Preferred Reporting Items for Systematic Reviews and Meta-Analysis (PRISMA) protocol using the PubMed, Scopus, and CINAHL databases. We registered our systematic review protocol in PROSPERO under registration number CRD42021270050. Human intervention studies published until April 30, 2023, were included. The quality of the included studies was assessed using National Institutes of Health (NIH) quality assessment study tools for intervention studies. The search in the database returned 166 studies, of which 13 matched all criteria for the final qualitative analysis. The body of evidence suggests that IF modulates human gut microbiota alpha and beta diversity in lean (relatively healthy) and relatively healthy overweight/obese individuals but not in individuals with metabolic syndrome. Furthermore, IF also alters human gut microbiota composition in all phenotypes. Of interest, the gut microbiota taxa or microbial metabolites after an IF intervention are associated with metabolic markers. According to this review, IF influences the diversity and taxonomic levels of the human gut microbiota. Individual metabolic phenotypes may alter the effect of IF on the diversity and taxonomic levels of the gut microbiota.

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