Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia

Abstract 16S rRNA sequencing of human fecal samples has been tremendously successful in identifying microbiome changes associated with both aging and disease. A number of studies have described microbial alterations corresponding to physical frailty and nursing home residence among aging individuals...

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Main Authors: Lin Kang, Pengtao Li, Danyang Wang, Taihao Wang, Dong Hao, Xuan Qu
Format: Article
Language:English
Published: Nature Publishing Group 2021-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-84031-0
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spelling doaj-ee5ab244d47b49f2abf3fb935bef0b2b2021-03-11T12:13:27ZengNature Publishing GroupScientific Reports2045-23222021-02-0111111410.1038/s41598-021-84031-0Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopeniaLin Kang0Pengtao Li1Danyang Wang2Taihao Wang3Dong Hao4Xuan Qu5Department of Geriatrics, Peking Union Medical College HospitalAllwegene Technology Inc.Department of Geriatrics, Urumqi Friendship HospitalDepartment of Geriatrics Centre, Hainan General HospitalDepartment of Geriatrics, Liaocheng People’s HospitalDepartment of Geriatrics, Peking Union Medical College HospitalAbstract 16S rRNA sequencing of human fecal samples has been tremendously successful in identifying microbiome changes associated with both aging and disease. A number of studies have described microbial alterations corresponding to physical frailty and nursing home residence among aging individuals. A gut-muscle axis through which the microbiome influences skeletal muscle growth/function has been hypothesized. However, the microbiome has yet to be examined in sarcopenia. Here, we collected fecal samples of 60 healthy controls (CON) and 27 sarcopenic (Case)/possibly sarcopenic (preCase) individuals and analyzed the intestinal microbiota using 16S rRNA sequencing. We observed an overall reduction in microbial diversity in Case and preCase samples. The genera Lachnospira, Fusicantenibacter, Roseburia, Eubacterium, and Lachnoclostridium—known butyrate producers—were significantly less abundant in Case and preCase subjects while Lactobacillus was more abundant. Functional pathways underrepresented in Case subjects included numerous transporters and phenylalanine, tyrosine, and tryptophan biosynthesis suggesting that protein processing and nutrient transport may be impaired. In contrast, lipopolysaccharide biosynthesis was overrepresented in Case and PreCase subjects suggesting that sarcopenia is associated with a pro-inflammatory metagenome. These analyses demonstrate structural and functional alterations in the intestinal microbiota that may contribute to loss of skeletal muscle mass and function in sarcopenia.https://doi.org/10.1038/s41598-021-84031-0
collection DOAJ
language English
format Article
sources DOAJ
author Lin Kang
Pengtao Li
Danyang Wang
Taihao Wang
Dong Hao
Xuan Qu
spellingShingle Lin Kang
Pengtao Li
Danyang Wang
Taihao Wang
Dong Hao
Xuan Qu
Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
Scientific Reports
author_facet Lin Kang
Pengtao Li
Danyang Wang
Taihao Wang
Dong Hao
Xuan Qu
author_sort Lin Kang
title Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
title_short Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
title_full Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
title_fullStr Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
title_full_unstemmed Alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
title_sort alterations in intestinal microbiota diversity, composition, and function in patients with sarcopenia
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2021-02-01
description Abstract 16S rRNA sequencing of human fecal samples has been tremendously successful in identifying microbiome changes associated with both aging and disease. A number of studies have described microbial alterations corresponding to physical frailty and nursing home residence among aging individuals. A gut-muscle axis through which the microbiome influences skeletal muscle growth/function has been hypothesized. However, the microbiome has yet to be examined in sarcopenia. Here, we collected fecal samples of 60 healthy controls (CON) and 27 sarcopenic (Case)/possibly sarcopenic (preCase) individuals and analyzed the intestinal microbiota using 16S rRNA sequencing. We observed an overall reduction in microbial diversity in Case and preCase samples. The genera Lachnospira, Fusicantenibacter, Roseburia, Eubacterium, and Lachnoclostridium—known butyrate producers—were significantly less abundant in Case and preCase subjects while Lactobacillus was more abundant. Functional pathways underrepresented in Case subjects included numerous transporters and phenylalanine, tyrosine, and tryptophan biosynthesis suggesting that protein processing and nutrient transport may be impaired. In contrast, lipopolysaccharide biosynthesis was overrepresented in Case and PreCase subjects suggesting that sarcopenia is associated with a pro-inflammatory metagenome. These analyses demonstrate structural and functional alterations in the intestinal microbiota that may contribute to loss of skeletal muscle mass and function in sarcopenia.
url https://doi.org/10.1038/s41598-021-84031-0
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