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Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study
Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause progressive exercise intolerance during cardiopulmonary exercise testing (CPET), and may contribute to the development of chronic respiratory insufficiency. The aim of this study is to evaluate exerci...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131603/ https://www.ncbi.nlm.nih.gov/pubmed/30234080 http://dx.doi.org/10.3389/fped.2018.00244 |
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author | Sovtic, Aleksandar Minic, Predrag Markovic-Sovtic, Gordana Trajkovic, Goran Z. |
author_facet | Sovtic, Aleksandar Minic, Predrag Markovic-Sovtic, Gordana Trajkovic, Goran Z. |
author_sort | Sovtic, Aleksandar |
collection | PubMed |
description | Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause progressive exercise intolerance during cardiopulmonary exercise testing (CPET), and may contribute to the development of chronic respiratory insufficiency. The aim of this study is to evaluate exercise tolerance during CPET of children and adults with clinically stable CF who exhibit different respiratory muscle strength. Methods: Sixty-nine clinically stable CF subjects aged 8–33 years underwent spirometry, body plethysmography, CPET, and respiratory muscle strength measurement. Respiratory muscle strength was measured using maximal inspiratory pressures (Pi(max)) and maximal expiratory pressures (Pe(max)). Participants were stratified into three groups according to Pi(max) values:below normal (≤80% predicted), normal (81–100% predicted), and above normal (>100% predicted). A similar stratification of participants was made according to Pe(max) values. The oxygen consumption on peak load (VO(2peak)) was expressed relative to BM (VO(2peak)/kg), relative to BM raised by the exponent of 0.67 (VO(2peak)/kg(0.67)) and as log-linear adjustment of VO(2peak) (VO(2peak/kg−alo)). Results: Participants with low Pe(max) values had a lower mean maximum load per kilogram/predicted (W(max); p = 0.001) VO(2peak)/kg (p = 0.006), VO(2peak)/kg(0.67) (p = 0.038) and VO(2peak/kg−alo) (p = 0.001). There were no significant differences in exercise tolerance parameters with regard to Pi(max) values. Stepwise multiple linear regressions confirmed that Pe(max) (B = 24.88, β = 0.48, p < 0.001) was the most powerful predictor of W(max). There were no statistically significant differences in age, lung function parameters, exacerbation score, or respiratory muscle strength according to gender. Conclusions: In subjects with clinically stable CF, expiratory muscle strength is associated with a decrease in exercise performance during CPET and can predict exercise intolerance. Increase in expiratory muscle strength by patient specific rehabilitation protocols would result in improvement of exercise tolerance. |
format | Online Article Text |
id | pubmed-6131603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-61316032018-09-19 Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study Sovtic, Aleksandar Minic, Predrag Markovic-Sovtic, Gordana Trajkovic, Goran Z. Front Pediatr Pediatrics Introduction: Decreased respiratory muscle strength in patients with cystic fibrosis (CF) may cause progressive exercise intolerance during cardiopulmonary exercise testing (CPET), and may contribute to the development of chronic respiratory insufficiency. The aim of this study is to evaluate exercise tolerance during CPET of children and adults with clinically stable CF who exhibit different respiratory muscle strength. Methods: Sixty-nine clinically stable CF subjects aged 8–33 years underwent spirometry, body plethysmography, CPET, and respiratory muscle strength measurement. Respiratory muscle strength was measured using maximal inspiratory pressures (Pi(max)) and maximal expiratory pressures (Pe(max)). Participants were stratified into three groups according to Pi(max) values:below normal (≤80% predicted), normal (81–100% predicted), and above normal (>100% predicted). A similar stratification of participants was made according to Pe(max) values. The oxygen consumption on peak load (VO(2peak)) was expressed relative to BM (VO(2peak)/kg), relative to BM raised by the exponent of 0.67 (VO(2peak)/kg(0.67)) and as log-linear adjustment of VO(2peak) (VO(2peak/kg−alo)). Results: Participants with low Pe(max) values had a lower mean maximum load per kilogram/predicted (W(max); p = 0.001) VO(2peak)/kg (p = 0.006), VO(2peak)/kg(0.67) (p = 0.038) and VO(2peak/kg−alo) (p = 0.001). There were no significant differences in exercise tolerance parameters with regard to Pi(max) values. Stepwise multiple linear regressions confirmed that Pe(max) (B = 24.88, β = 0.48, p < 0.001) was the most powerful predictor of W(max). There were no statistically significant differences in age, lung function parameters, exacerbation score, or respiratory muscle strength according to gender. Conclusions: In subjects with clinically stable CF, expiratory muscle strength is associated with a decrease in exercise performance during CPET and can predict exercise intolerance. Increase in expiratory muscle strength by patient specific rehabilitation protocols would result in improvement of exercise tolerance. Frontiers Media S.A. 2018-09-04 /pmc/articles/PMC6131603/ /pubmed/30234080 http://dx.doi.org/10.3389/fped.2018.00244 Text en Copyright © 2018 Sovtic, Minic, Markovic-Sovtic and Trajkovic. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pediatrics Sovtic, Aleksandar Minic, Predrag Markovic-Sovtic, Gordana Trajkovic, Goran Z. Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study |
title | Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study |
title_full | Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study |
title_fullStr | Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study |
title_full_unstemmed | Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study |
title_short | Respiratory Muscle Strength and Exercise Performance in Cystic Fibrosis–A Cross Sectional Study |
title_sort | respiratory muscle strength and exercise performance in cystic fibrosis–a cross sectional study |
topic | Pediatrics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131603/ https://www.ncbi.nlm.nih.gov/pubmed/30234080 http://dx.doi.org/10.3389/fped.2018.00244 |
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