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Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals

PURPOSE: This pilot study investigated differences in lean tissue mass, muscle strength, muscle quality (strength per unit of muscle mass; MQ), and functional performance in healthy younger and older individuals. The most robust predictors of appendicular lean mass (ALM) were then determined in each...

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Autores principales: Lees, Matthew J., Wilson, Oliver J., Hind, Karen, Ispoglou, Theocharis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469623/
https://www.ncbi.nlm.nih.gov/pubmed/30806780
http://dx.doi.org/10.1007/s00421-019-04107-8
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author Lees, Matthew J.
Wilson, Oliver J.
Hind, Karen
Ispoglou, Theocharis
author_facet Lees, Matthew J.
Wilson, Oliver J.
Hind, Karen
Ispoglou, Theocharis
author_sort Lees, Matthew J.
collection PubMed
description PURPOSE: This pilot study investigated differences in lean tissue mass, muscle strength, muscle quality (strength per unit of muscle mass; MQ), and functional performance in healthy younger and older individuals. The most robust predictors of appendicular lean mass (ALM) were then determined in each group. METHODS: Fifty younger (18–45 years) and 50 older (60–80 years) participants completed tests of upper and lower body strength alongside body composition by dual-energy X-ray absorptiometry from which upper- and lower-body MQ were estimated. Available cut-points for older people were used to determine low upper-body MQ in both groups. Low lower-body MQ was determined as at least two standard deviations below the mean of the younger group. Functional performance was assessed by gait speed. Sarcopenia was identified using two established definitions. RESULTS: Upper and lower body strength, ALM, lower-body MQ and gait speed were significantly higher in the younger group (all p < 0.002). Sarcopenia was identified in 2–4% of the older group. Low upper-body MQ was evident in 32% and 42% of the younger and older group, respectively. Low lower-body MQ was observed in 4% of younger participants, and 50% of older participants. In both groups, the most robust predictors of ALM were upper and lower body strength (young R(2) = 0.74, 0.82; older R(2) = 0.68, 0.72). CONCLUSIONS: Low MQ despite low prevalence rates of sarcopenia in both groups suggests a need for age-specific MQ cut-points. Muscle quality assessments might be useful complementary prognostic tools alongside existing sarcopenia definitions.
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spelling pubmed-64696232019-05-03 Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals Lees, Matthew J. Wilson, Oliver J. Hind, Karen Ispoglou, Theocharis Eur J Appl Physiol Original Article PURPOSE: This pilot study investigated differences in lean tissue mass, muscle strength, muscle quality (strength per unit of muscle mass; MQ), and functional performance in healthy younger and older individuals. The most robust predictors of appendicular lean mass (ALM) were then determined in each group. METHODS: Fifty younger (18–45 years) and 50 older (60–80 years) participants completed tests of upper and lower body strength alongside body composition by dual-energy X-ray absorptiometry from which upper- and lower-body MQ were estimated. Available cut-points for older people were used to determine low upper-body MQ in both groups. Low lower-body MQ was determined as at least two standard deviations below the mean of the younger group. Functional performance was assessed by gait speed. Sarcopenia was identified using two established definitions. RESULTS: Upper and lower body strength, ALM, lower-body MQ and gait speed were significantly higher in the younger group (all p < 0.002). Sarcopenia was identified in 2–4% of the older group. Low upper-body MQ was evident in 32% and 42% of the younger and older group, respectively. Low lower-body MQ was observed in 4% of younger participants, and 50% of older participants. In both groups, the most robust predictors of ALM were upper and lower body strength (young R(2) = 0.74, 0.82; older R(2) = 0.68, 0.72). CONCLUSIONS: Low MQ despite low prevalence rates of sarcopenia in both groups suggests a need for age-specific MQ cut-points. Muscle quality assessments might be useful complementary prognostic tools alongside existing sarcopenia definitions. Springer Berlin Heidelberg 2019-02-26 2019 /pmc/articles/PMC6469623/ /pubmed/30806780 http://dx.doi.org/10.1007/s00421-019-04107-8 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Lees, Matthew J.
Wilson, Oliver J.
Hind, Karen
Ispoglou, Theocharis
Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals
title Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals
title_full Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals
title_fullStr Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals
title_full_unstemmed Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals
title_short Muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals
title_sort muscle quality as a complementary prognostic tool in conjunction with sarcopenia assessment in younger and older individuals
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6469623/
https://www.ncbi.nlm.nih.gov/pubmed/30806780
http://dx.doi.org/10.1007/s00421-019-04107-8
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