Age-related sarcopenia and altered gut microbiota: A systematic review

普氏粪杆菌 肌萎缩 蔷薇花 肠道菌群 生物 微生物学 拟杆菌 乳酸菌 真细菌 生理学 粪便 生物化学 内分泌学 细菌 遗传学 发酵
作者
Mengyu Wang,Fangyuan Ren,Yan Zhou,He Yuan,Taorui Du,Yurong Tan
出处
期刊:Microbial Pathogenesis [Elsevier BV]
卷期号:195: 106850-106850 被引量:3
标识
DOI:10.1016/j.micpath.2024.106850
摘要

Sarcopenia, a hallmark of age-related muscle function decline, significantly impacts elderly physical health. This systematic review aimed to investigate the impact of gut microbiota on sarcopenia. Publications up to September 24, 2023 were scrutinized on four databases - PubMed, Web of Science, Cochrane Library, and Embase - using relevant keywords. Non-English papers were disregarded. Data regarding gut microbiota alterations in sarcopenic patients/animal models were collected and examined. Thirteen human and eight animal studies were included. The human studies involved 732 sarcopenic or potentially sarcopenic participants (aged 57–98) and 2559 healthy subjects (aged 54–84). Animal studies encompassed five mouse and three rat experiments. Results indicated an increase in opportunistic pathogens like Enterobacteriaceae, accompanied by changes in several metabolite-related organisms. For example, Bacteroides fluxus related to horse uric acid metabolism exhibited increased abundance. However, Roseburia, Faecalibacterium, Faecalibacterium prausnitzii, Eubacterium retale, Akkermansiaa, Coprococcus, Clostridium_XIVa, Ruminococcaceae, Bacteroides, Clostridium, Eubacterium involved in urolithin A production, and Lactobacillus, Bacteroides, and Clostridium associated with bile acid metabolism displayed decreased abundance. Age-related sarcopenia and gut microbiota alterations are intricately linked. Short-chain fatty acid metabolism, urolithin A, and bile acid production may be pivotal factors in the gut-muscle axis pathway. Supplementation with beneficial metabolite-associated microorganisms could enhance muscle function, mitigate muscle atrophy, and decelerate sarcopenia progression.
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