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Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis

BACKGROUND: Mitochondrial dysfunction has been implicated in the pathogenesis of multiple sclerosis (MS). Whether mitochondrial alterations are a function of ambulatory dysfunction or are of a non-ambulatory systemic nature is unclear. OBJECTIVE: To compare oxidative capacity, and rest muscle oxygen...

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Autores principales: DePauw, Elizabeth M, Rouhani, Mitra, Flanagan, Aidan M, Ng, Alexander V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246512/
https://www.ncbi.nlm.nih.gov/pubmed/34262786
http://dx.doi.org/10.1177/20552173211028875
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author DePauw, Elizabeth M
Rouhani, Mitra
Flanagan, Aidan M
Ng, Alexander V
author_facet DePauw, Elizabeth M
Rouhani, Mitra
Flanagan, Aidan M
Ng, Alexander V
author_sort DePauw, Elizabeth M
collection PubMed
description BACKGROUND: Mitochondrial dysfunction has been implicated in the pathogenesis of multiple sclerosis (MS). Whether mitochondrial alterations are a function of ambulatory dysfunction or are of a non-ambulatory systemic nature is unclear. OBJECTIVE: To compare oxidative capacity, and rest muscle oxygen consumption (mVO(2)) in the upper limb of persons with multiple sclerosis (PwMS) to a control group (CON), whereby an upper limb would be comparatively independent of ambulation or deconditioning. METHODS: Near infra-red spectroscopy was used to measure oxidative capacity of the wrist flexors in PwMS (n = 16) and CON (n = 13). Oxidative capacity was indicated by the time constant (TC) of mVO(2) recovery following brief wrist flexion contractions. Measurements included well-being, depression, symptomatic fatigue, disability, handgrip strength, cognition, and functional endurance. Analysis was by T-tests and Pearson correlations with p ≤ 0.05. Data are mean (SD). RESULTS: TC of mVO(2) recovery was slower in PwMS (MS = 47(14) sec, CON = 36(11) sec; p = 0.03). No significant correlations were found between oxidative capacity and any other measures. Rest mVO(2) was not different between groups, but correlated with symptomatic fatigue (r = 0.694, p = 0.003) and strength (0.585, p = 0.017) in PwMS. CONCLUSION: Oxidative capacity was lower in the wrist flexors of PwMS, possibly indicating a systemic component of the disease. Within PwMS, rest mVO(2) was associated with symptomatic fatigue.
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spelling pubmed-82465122021-07-13 Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis DePauw, Elizabeth M Rouhani, Mitra Flanagan, Aidan M Ng, Alexander V Mult Scler J Exp Transl Clin Original Research Article BACKGROUND: Mitochondrial dysfunction has been implicated in the pathogenesis of multiple sclerosis (MS). Whether mitochondrial alterations are a function of ambulatory dysfunction or are of a non-ambulatory systemic nature is unclear. OBJECTIVE: To compare oxidative capacity, and rest muscle oxygen consumption (mVO(2)) in the upper limb of persons with multiple sclerosis (PwMS) to a control group (CON), whereby an upper limb would be comparatively independent of ambulation or deconditioning. METHODS: Near infra-red spectroscopy was used to measure oxidative capacity of the wrist flexors in PwMS (n = 16) and CON (n = 13). Oxidative capacity was indicated by the time constant (TC) of mVO(2) recovery following brief wrist flexion contractions. Measurements included well-being, depression, symptomatic fatigue, disability, handgrip strength, cognition, and functional endurance. Analysis was by T-tests and Pearson correlations with p ≤ 0.05. Data are mean (SD). RESULTS: TC of mVO(2) recovery was slower in PwMS (MS = 47(14) sec, CON = 36(11) sec; p = 0.03). No significant correlations were found between oxidative capacity and any other measures. Rest mVO(2) was not different between groups, but correlated with symptomatic fatigue (r = 0.694, p = 0.003) and strength (0.585, p = 0.017) in PwMS. CONCLUSION: Oxidative capacity was lower in the wrist flexors of PwMS, possibly indicating a systemic component of the disease. Within PwMS, rest mVO(2) was associated with symptomatic fatigue. SAGE Publications 2021-06-24 /pmc/articles/PMC8246512/ /pubmed/34262786 http://dx.doi.org/10.1177/20552173211028875 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research Article
DePauw, Elizabeth M
Rouhani, Mitra
Flanagan, Aidan M
Ng, Alexander V
Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis
title Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis
title_full Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis
title_fullStr Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis
title_full_unstemmed Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis
title_short Forearm muscle mitochondrial capacity and resting oxygen uptake: Relationship to symptomatic fatigue in persons with multiple sclerosis
title_sort forearm muscle mitochondrial capacity and resting oxygen uptake: relationship to symptomatic fatigue in persons with multiple sclerosis
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8246512/
https://www.ncbi.nlm.nih.gov/pubmed/34262786
http://dx.doi.org/10.1177/20552173211028875
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