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Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes

The longitudinal monitoring of oxidative stress (OS) in athletes may enable the identification of fatigued states and underperformance. The application of OS biomarker monitoring programs in sport are hindered by reliability and repeatability of in-the-field testing tools, the turnaround of results,...

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Autores principales: Lewis, Nathan A., Newell, John, Burden, Richard, Howatson, Glyn, Pedlar, Charles R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773226/
https://www.ncbi.nlm.nih.gov/pubmed/26930475
http://dx.doi.org/10.1371/journal.pone.0149927
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author Lewis, Nathan A.
Newell, John
Burden, Richard
Howatson, Glyn
Pedlar, Charles R.
author_facet Lewis, Nathan A.
Newell, John
Burden, Richard
Howatson, Glyn
Pedlar, Charles R.
author_sort Lewis, Nathan A.
collection PubMed
description The longitudinal monitoring of oxidative stress (OS) in athletes may enable the identification of fatigued states and underperformance. The application of OS biomarker monitoring programs in sport are hindered by reliability and repeatability of in-the-field testing tools, the turnaround of results, and the understanding of biological variation (BV). Knowledge of BV and critical difference values (CDV) may assist with data interpretation in the individual athlete. Methods: We aimed firstly to assess the repeatability of the clinical point of care redox test, Free Oxygen Radical Test (FORT) and the Free Oxygen Radical Defence (FORD) in trained participants and elite athletes and secondly to calculate the analytical, BV, CDV and index of individuality (II) for FORT, FORD, red blood cell glutathione, lutein, α and γ–tocopherol. Part 1: Fifteen elite athletes were sampled in duplicate for calculation of the repeatability of the FORT and FORD tests. Part 2: Twelve well-trained athletes had venous samples drawn every 2 hours from 0800 to 1800 for calculation of BV, CDV, II for FORT, FORD, RBC GSH, lutein, α-tocopherol and γ–tocopherol. Results: Repeatability of the FORT and FORD assay was 3.9% and 3.7% respectively. Biomarker CDV ranged from 12.8% to 37%, with a circadian effect for FORT, α-tocopherol and γ-tocopherol (p<0.01), with all biomarker indices of individuality < 0.8 arbitrary units. Conclusion: We report that the use of the novel redox test in athletes is practical, and the generation of BV and CDV for biomarkers of OS enhances the interpretation of physiologically meaningful changes in individuals above the use of clinical reference ranges alone.
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spelling pubmed-47732262016-03-07 Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes Lewis, Nathan A. Newell, John Burden, Richard Howatson, Glyn Pedlar, Charles R. PLoS One Research Article The longitudinal monitoring of oxidative stress (OS) in athletes may enable the identification of fatigued states and underperformance. The application of OS biomarker monitoring programs in sport are hindered by reliability and repeatability of in-the-field testing tools, the turnaround of results, and the understanding of biological variation (BV). Knowledge of BV and critical difference values (CDV) may assist with data interpretation in the individual athlete. Methods: We aimed firstly to assess the repeatability of the clinical point of care redox test, Free Oxygen Radical Test (FORT) and the Free Oxygen Radical Defence (FORD) in trained participants and elite athletes and secondly to calculate the analytical, BV, CDV and index of individuality (II) for FORT, FORD, red blood cell glutathione, lutein, α and γ–tocopherol. Part 1: Fifteen elite athletes were sampled in duplicate for calculation of the repeatability of the FORT and FORD tests. Part 2: Twelve well-trained athletes had venous samples drawn every 2 hours from 0800 to 1800 for calculation of BV, CDV, II for FORT, FORD, RBC GSH, lutein, α-tocopherol and γ–tocopherol. Results: Repeatability of the FORT and FORD assay was 3.9% and 3.7% respectively. Biomarker CDV ranged from 12.8% to 37%, with a circadian effect for FORT, α-tocopherol and γ-tocopherol (p<0.01), with all biomarker indices of individuality < 0.8 arbitrary units. Conclusion: We report that the use of the novel redox test in athletes is practical, and the generation of BV and CDV for biomarkers of OS enhances the interpretation of physiologically meaningful changes in individuals above the use of clinical reference ranges alone. Public Library of Science 2016-03-01 /pmc/articles/PMC4773226/ /pubmed/26930475 http://dx.doi.org/10.1371/journal.pone.0149927 Text en © 2016 Lewis et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Lewis, Nathan A.
Newell, John
Burden, Richard
Howatson, Glyn
Pedlar, Charles R.
Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes
title Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes
title_full Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes
title_fullStr Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes
title_full_unstemmed Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes
title_short Critical Difference and Biological Variation in Biomarkers of Oxidative Stress and Nutritional Status in Athletes
title_sort critical difference and biological variation in biomarkers of oxidative stress and nutritional status in athletes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4773226/
https://www.ncbi.nlm.nih.gov/pubmed/26930475
http://dx.doi.org/10.1371/journal.pone.0149927
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