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Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum
The study aim was to compare the predictive validity of the often referenced traditional model of human endurance performance (i.e. oxygen consumption, VO(2), or power at maximal effort, fatigue threshold values, and indices of exercise efficiency) versus measures of skeletal muscle oxidative potent...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971325/ https://www.ncbi.nlm.nih.gov/pubmed/31960629 http://dx.doi.org/10.14814/phy2.14342 |
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author | Batterson, Philip M. Norton, Michael R. Hetz, Sarah E. Rohilla, Sachi Lindsay, Keston G. Subudhi, Andrew W. Jacobs, Robert A. |
author_facet | Batterson, Philip M. Norton, Michael R. Hetz, Sarah E. Rohilla, Sachi Lindsay, Keston G. Subudhi, Andrew W. Jacobs, Robert A. |
author_sort | Batterson, Philip M. |
collection | PubMed |
description | The study aim was to compare the predictive validity of the often referenced traditional model of human endurance performance (i.e. oxygen consumption, VO(2), or power at maximal effort, fatigue threshold values, and indices of exercise efficiency) versus measures of skeletal muscle oxidative potential in relation to endurance cycling performance. We hypothesized that skeletal muscle oxidative potential would more completely explain endurance performance than the traditional model, which has never been collectively verified with cycling. Accordingly, we obtained nine measures of VO(2) or power at maximal efforts, 20 measures reflective of various fatigue threshold values, 14 indices of cycling efficiency, and near‐infrared spectroscopy‐derived measures reflecting in vivo skeletal muscle oxidative potential. Forward regression modeling identified variable combinations that best explained 25‐km time trial time‐to‐completion (TTC) across a group of trained male participants (n = 24). The time constant for skeletal muscle oxygen consumption recovery, a validated measure of maximal skeletal muscle respiration, explained 92.7% of TTC variance by itself (Adj R (2) = .927, F = 294.2, SEE = 71.2, p < .001). Alternatively, the best complete traditional model of performance, including VO(2max) (L·min(−1)), %VO(2max) determined by the ventilatory equivalents method, and cycling economy at 50 W, only explained 76.2% of TTC variance (Adj R (2) = .762, F = 25.6, SEE = 128.7, p < .001). These results confirm our hypothesis by demonstrating that maximal rates of skeletal muscle respiration more completely explain cycling endurance performance than even the best combination of traditional variables long postulated to predict human endurance performance. |
format | Online Article Text |
id | pubmed-6971325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69713252020-01-27 Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum Batterson, Philip M. Norton, Michael R. Hetz, Sarah E. Rohilla, Sachi Lindsay, Keston G. Subudhi, Andrew W. Jacobs, Robert A. Physiol Rep Original Research The study aim was to compare the predictive validity of the often referenced traditional model of human endurance performance (i.e. oxygen consumption, VO(2), or power at maximal effort, fatigue threshold values, and indices of exercise efficiency) versus measures of skeletal muscle oxidative potential in relation to endurance cycling performance. We hypothesized that skeletal muscle oxidative potential would more completely explain endurance performance than the traditional model, which has never been collectively verified with cycling. Accordingly, we obtained nine measures of VO(2) or power at maximal efforts, 20 measures reflective of various fatigue threshold values, 14 indices of cycling efficiency, and near‐infrared spectroscopy‐derived measures reflecting in vivo skeletal muscle oxidative potential. Forward regression modeling identified variable combinations that best explained 25‐km time trial time‐to‐completion (TTC) across a group of trained male participants (n = 24). The time constant for skeletal muscle oxygen consumption recovery, a validated measure of maximal skeletal muscle respiration, explained 92.7% of TTC variance by itself (Adj R (2) = .927, F = 294.2, SEE = 71.2, p < .001). Alternatively, the best complete traditional model of performance, including VO(2max) (L·min(−1)), %VO(2max) determined by the ventilatory equivalents method, and cycling economy at 50 W, only explained 76.2% of TTC variance (Adj R (2) = .762, F = 25.6, SEE = 128.7, p < .001). These results confirm our hypothesis by demonstrating that maximal rates of skeletal muscle respiration more completely explain cycling endurance performance than even the best combination of traditional variables long postulated to predict human endurance performance. John Wiley and Sons Inc. 2020-01-20 /pmc/articles/PMC6971325/ /pubmed/31960629 http://dx.doi.org/10.14814/phy2.14342 Text en © 2020 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Batterson, Philip M. Norton, Michael R. Hetz, Sarah E. Rohilla, Sachi Lindsay, Keston G. Subudhi, Andrew W. Jacobs, Robert A. Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum |
title | Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum |
title_full | Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum |
title_fullStr | Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum |
title_full_unstemmed | Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum |
title_short | Improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: E pluribus unum |
title_sort | improving biologic predictors of cycling endurance performance with near‐infrared spectroscopy derived measures of skeletal muscle respiration: e pluribus unum |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6971325/ https://www.ncbi.nlm.nih.gov/pubmed/31960629 http://dx.doi.org/10.14814/phy2.14342 |
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