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Metabolic Syndrome and Sarcopenia
Skeletal muscle is a major organ of insulin-induced glucose metabolism. In addition, loss of muscle mass is closely linked to insulin resistance (IR) and metabolic syndrome (Met-S). Skeletal muscle loss and accumulation of intramuscular fat are associated with a variety of pathologies through a comb...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541622/ https://www.ncbi.nlm.nih.gov/pubmed/34684520 http://dx.doi.org/10.3390/nu13103519 |
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author | Nishikawa, Hiroki Asai, Akira Fukunishi, Shinya Nishiguchi, Shuhei Higuchi, Kazuhide |
author_facet | Nishikawa, Hiroki Asai, Akira Fukunishi, Shinya Nishiguchi, Shuhei Higuchi, Kazuhide |
author_sort | Nishikawa, Hiroki |
collection | PubMed |
description | Skeletal muscle is a major organ of insulin-induced glucose metabolism. In addition, loss of muscle mass is closely linked to insulin resistance (IR) and metabolic syndrome (Met-S). Skeletal muscle loss and accumulation of intramuscular fat are associated with a variety of pathologies through a combination of factors, including oxidative stress, inflammatory cytokines, mitochondrial dysfunction, IR, and inactivity. Sarcopenia, defined by a loss of muscle mass and a decline in muscle quality and muscle function, is common in the elderly and is also often seen in patients with acute or chronic muscle-wasting diseases. The relationship between Met-S and sarcopenia has been attracting a great deal of attention these days. Persistent inflammation, fat deposition, and IR are thought to play a complex role in the association between Met-S and sarcopenia. Met-S and sarcopenia adversely affect QOL and contribute to increased frailty, weakness, dependence, and morbidity and mortality. Patients with Met-S and sarcopenia at the same time have a higher risk of several adverse health events than those with either Met-S or sarcopenia. Met-S can also be associated with sarcopenic obesity. In this review, the relationship between Met-S and sarcopenia will be outlined from the viewpoints of molecular mechanism and clinical impact. |
format | Online Article Text |
id | pubmed-8541622 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-85416222021-10-24 Metabolic Syndrome and Sarcopenia Nishikawa, Hiroki Asai, Akira Fukunishi, Shinya Nishiguchi, Shuhei Higuchi, Kazuhide Nutrients Review Skeletal muscle is a major organ of insulin-induced glucose metabolism. In addition, loss of muscle mass is closely linked to insulin resistance (IR) and metabolic syndrome (Met-S). Skeletal muscle loss and accumulation of intramuscular fat are associated with a variety of pathologies through a combination of factors, including oxidative stress, inflammatory cytokines, mitochondrial dysfunction, IR, and inactivity. Sarcopenia, defined by a loss of muscle mass and a decline in muscle quality and muscle function, is common in the elderly and is also often seen in patients with acute or chronic muscle-wasting diseases. The relationship between Met-S and sarcopenia has been attracting a great deal of attention these days. Persistent inflammation, fat deposition, and IR are thought to play a complex role in the association between Met-S and sarcopenia. Met-S and sarcopenia adversely affect QOL and contribute to increased frailty, weakness, dependence, and morbidity and mortality. Patients with Met-S and sarcopenia at the same time have a higher risk of several adverse health events than those with either Met-S or sarcopenia. Met-S can also be associated with sarcopenic obesity. In this review, the relationship between Met-S and sarcopenia will be outlined from the viewpoints of molecular mechanism and clinical impact. MDPI 2021-10-07 /pmc/articles/PMC8541622/ /pubmed/34684520 http://dx.doi.org/10.3390/nu13103519 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Nishikawa, Hiroki Asai, Akira Fukunishi, Shinya Nishiguchi, Shuhei Higuchi, Kazuhide Metabolic Syndrome and Sarcopenia |
title | Metabolic Syndrome and Sarcopenia |
title_full | Metabolic Syndrome and Sarcopenia |
title_fullStr | Metabolic Syndrome and Sarcopenia |
title_full_unstemmed | Metabolic Syndrome and Sarcopenia |
title_short | Metabolic Syndrome and Sarcopenia |
title_sort | metabolic syndrome and sarcopenia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8541622/ https://www.ncbi.nlm.nih.gov/pubmed/34684520 http://dx.doi.org/10.3390/nu13103519 |
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