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Understanding the gut microbiota and sarcopenia: a systematic review

BACKGROUND: Gut microbiota dysbiosis and sarcopenia commonly occur in the elderly. Although the concept of the gut–muscle axis has been raised, the casual relationship is still unclear. This systematic review analyses the current evidence of gut microbiota effects on muscle/sarcopenia. METHODS: A sy...

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Autores principales: Liu, Chaoran, Cheung, Wing‐Hoi, Li, Jie, Chow, Simon Kwoon‐Ho, Yu, Jun, Wong, Sunny Hei, Ip, Margaret, Sung, Joseph Jao Yiu, Wong, Ronald Man Yeung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718038/
https://www.ncbi.nlm.nih.gov/pubmed/34523250
http://dx.doi.org/10.1002/jcsm.12784
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author Liu, Chaoran
Cheung, Wing‐Hoi
Li, Jie
Chow, Simon Kwoon‐Ho
Yu, Jun
Wong, Sunny Hei
Ip, Margaret
Sung, Joseph Jao Yiu
Wong, Ronald Man Yeung
author_facet Liu, Chaoran
Cheung, Wing‐Hoi
Li, Jie
Chow, Simon Kwoon‐Ho
Yu, Jun
Wong, Sunny Hei
Ip, Margaret
Sung, Joseph Jao Yiu
Wong, Ronald Man Yeung
author_sort Liu, Chaoran
collection PubMed
description BACKGROUND: Gut microbiota dysbiosis and sarcopenia commonly occur in the elderly. Although the concept of the gut–muscle axis has been raised, the casual relationship is still unclear. This systematic review analyses the current evidence of gut microbiota effects on muscle/sarcopenia. METHODS: A systematic review was performed in PubMed, Embase, Web of Science, and The Cochrane Library databases using the keywords (microbiota* OR microbiome*) AND (sarcopen* OR muscle). Studies reporting the alterations of gut microbiota and muscle/physical performance were analysed. RESULTS: A total of 26 pre‐clinical and 10 clinical studies were included. For animal studies, three revealed age‐related changes and relationships between gut microbiota and muscle. Three studies focused on muscle characteristics of germ‐free mice. Seventy‐five per cent of eight faecal microbiota transplantation studies showed that the recipient mice successfully replicated the muscle phenotype of donors. There were positive effects on muscle from seven probiotics, two prebiotics, and short‐chain fatty acids (SCFAs). Ten studies investigated on other dietary supplements, antibiotics, exercise, and food withdrawal that affected both muscle and gut microbiota. Twelve studies explored the potential mechanisms of the gut–muscle axis. For clinical studies, 6 studies recruited 676 elderly people (72.8 ± 5.6 years, 57.8% female), while 4 studies focused on 244 young adults (29.7 ± 7.8 years, 55.4% female). The associations of gut microbiota and muscle had been shown in four observational studies. Probiotics, prebiotics, synbiotics, fermented milk, caloric restriction, and exercise in six studies displayed inconsistent effects on muscle mass, function, and gut microbiota. CONCLUSIONS: Altering the gut microbiota through bacteria depletion, faecal transplantation, and various supplements was shown to directly affect muscle phenotypes. Probiotics, prebiotics, SCFAs, and bacterial products are potential novel therapies to enhance muscle mass and physical performance. Lactobacillus and Bifidobacterium strains restored age‐related muscle loss. Potential mechanisms of microbiome modulating muscle mainly include protein, energy, lipid, and glucose metabolism, inflammation level, neuromuscular junction, and mitochondrial function. The role of the gut microbiota in the development of muscle loss during aging is a crucial area that requires further studies for translation to patients.
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spelling pubmed-87180382022-01-06 Understanding the gut microbiota and sarcopenia: a systematic review Liu, Chaoran Cheung, Wing‐Hoi Li, Jie Chow, Simon Kwoon‐Ho Yu, Jun Wong, Sunny Hei Ip, Margaret Sung, Joseph Jao Yiu Wong, Ronald Man Yeung J Cachexia Sarcopenia Muscle Reviews BACKGROUND: Gut microbiota dysbiosis and sarcopenia commonly occur in the elderly. Although the concept of the gut–muscle axis has been raised, the casual relationship is still unclear. This systematic review analyses the current evidence of gut microbiota effects on muscle/sarcopenia. METHODS: A systematic review was performed in PubMed, Embase, Web of Science, and The Cochrane Library databases using the keywords (microbiota* OR microbiome*) AND (sarcopen* OR muscle). Studies reporting the alterations of gut microbiota and muscle/physical performance were analysed. RESULTS: A total of 26 pre‐clinical and 10 clinical studies were included. For animal studies, three revealed age‐related changes and relationships between gut microbiota and muscle. Three studies focused on muscle characteristics of germ‐free mice. Seventy‐five per cent of eight faecal microbiota transplantation studies showed that the recipient mice successfully replicated the muscle phenotype of donors. There were positive effects on muscle from seven probiotics, two prebiotics, and short‐chain fatty acids (SCFAs). Ten studies investigated on other dietary supplements, antibiotics, exercise, and food withdrawal that affected both muscle and gut microbiota. Twelve studies explored the potential mechanisms of the gut–muscle axis. For clinical studies, 6 studies recruited 676 elderly people (72.8 ± 5.6 years, 57.8% female), while 4 studies focused on 244 young adults (29.7 ± 7.8 years, 55.4% female). The associations of gut microbiota and muscle had been shown in four observational studies. Probiotics, prebiotics, synbiotics, fermented milk, caloric restriction, and exercise in six studies displayed inconsistent effects on muscle mass, function, and gut microbiota. CONCLUSIONS: Altering the gut microbiota through bacteria depletion, faecal transplantation, and various supplements was shown to directly affect muscle phenotypes. Probiotics, prebiotics, SCFAs, and bacterial products are potential novel therapies to enhance muscle mass and physical performance. Lactobacillus and Bifidobacterium strains restored age‐related muscle loss. Potential mechanisms of microbiome modulating muscle mainly include protein, energy, lipid, and glucose metabolism, inflammation level, neuromuscular junction, and mitochondrial function. The role of the gut microbiota in the development of muscle loss during aging is a crucial area that requires further studies for translation to patients. John Wiley and Sons Inc. 2021-09-14 2021-12 /pmc/articles/PMC8718038/ /pubmed/34523250 http://dx.doi.org/10.1002/jcsm.12784 Text en © 2021 The Authors. Journal of Cachexia, Sarcopenia and Muscle published by John Wiley & Sons Ltd on behalf of Society on Sarcopenia, Cachexia and Wasting Disorders. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Reviews
Liu, Chaoran
Cheung, Wing‐Hoi
Li, Jie
Chow, Simon Kwoon‐Ho
Yu, Jun
Wong, Sunny Hei
Ip, Margaret
Sung, Joseph Jao Yiu
Wong, Ronald Man Yeung
Understanding the gut microbiota and sarcopenia: a systematic review
title Understanding the gut microbiota and sarcopenia: a systematic review
title_full Understanding the gut microbiota and sarcopenia: a systematic review
title_fullStr Understanding the gut microbiota and sarcopenia: a systematic review
title_full_unstemmed Understanding the gut microbiota and sarcopenia: a systematic review
title_short Understanding the gut microbiota and sarcopenia: a systematic review
title_sort understanding the gut microbiota and sarcopenia: a systematic review
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8718038/
https://www.ncbi.nlm.nih.gov/pubmed/34523250
http://dx.doi.org/10.1002/jcsm.12784
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