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Circulating, cell-free DNA as a marker for exercise load in intermittent sports

BACKGROUND: Attempts to establish a biomarker reflecting individual player load in intermittent sports such as football have failed so far. Increases in circulating DNA (cfDNA) have been demonstrated in various endurance sports settings. While it has been proposed that cfDNA could be a suitable mark...

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Autores principales: Haller, Nils, Helmig, Susanne, Taenny, Pascal, Petry, Julian, Schmidt, Sebastian, Simon, Perikles
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784997/
https://www.ncbi.nlm.nih.gov/pubmed/29370268
http://dx.doi.org/10.1371/journal.pone.0191915
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author Haller, Nils
Helmig, Susanne
Taenny, Pascal
Petry, Julian
Schmidt, Sebastian
Simon, Perikles
author_facet Haller, Nils
Helmig, Susanne
Taenny, Pascal
Petry, Julian
Schmidt, Sebastian
Simon, Perikles
author_sort Haller, Nils
collection PubMed
description BACKGROUND: Attempts to establish a biomarker reflecting individual player load in intermittent sports such as football have failed so far. Increases in circulating DNA (cfDNA) have been demonstrated in various endurance sports settings. While it has been proposed that cfDNA could be a suitable marker for player load in intermittent sports, the effects on cfDNA of repeated sprinting as an essential feature in intermittent sports are unknown. For the first time, we assessed both alterations of cfDNA due to repeated maximal sprints and due to a professional football game. METHODS: Nine participants were subjected to a standardised sprint training session with cross-over design of five maximal sprints of 40 meters with either “short” (1 minute) or “long” pauses (5 minutes). Capillary cfDNA and lactate were measured after every sprint and venous cfDNA before and after each series of sprints. Moreover, capillary cfDNA and lactate values were taken in 23 professional football players before and after incremental exercise testing, during the course of a training week at rest (baseline) and in all 17 enrolled players following a season game. RESULTS: Lactate and venous cfDNA increased more pronounced during “short” compared to “long” (1.4-fold, p = 0.032 and 1.7-fold, p = 0.016) and cfDNA correlated significantly with lactate (r = 0.69; p<0.001). Incremental exercise testing increased cfDNA 7.0-fold (p<0.001). The season game increased cfDNA 22.7-fold (p<0.0001), while lactate showed a 2.0-fold (p = 0.09) increase compared to baseline. Fold-changes in cfDNA correlated with distance covered during game (spearman’s r = 0.87, p = 0.0012), while no correlation between lactate and the tracking data could be found. DISCUSSION: We show for the first time that cfDNA could be an objective marker for distance covered in elite intermittent sports. In contrast to the potential of more established blood-based markers like IL-6, CK, or CRP, cfDNA shows by far the strongest fold-change and a high correlation with a particular load related aspect in professional football.
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spelling pubmed-57849972018-02-09 Circulating, cell-free DNA as a marker for exercise load in intermittent sports Haller, Nils Helmig, Susanne Taenny, Pascal Petry, Julian Schmidt, Sebastian Simon, Perikles PLoS One Research Article BACKGROUND: Attempts to establish a biomarker reflecting individual player load in intermittent sports such as football have failed so far. Increases in circulating DNA (cfDNA) have been demonstrated in various endurance sports settings. While it has been proposed that cfDNA could be a suitable marker for player load in intermittent sports, the effects on cfDNA of repeated sprinting as an essential feature in intermittent sports are unknown. For the first time, we assessed both alterations of cfDNA due to repeated maximal sprints and due to a professional football game. METHODS: Nine participants were subjected to a standardised sprint training session with cross-over design of five maximal sprints of 40 meters with either “short” (1 minute) or “long” pauses (5 minutes). Capillary cfDNA and lactate were measured after every sprint and venous cfDNA before and after each series of sprints. Moreover, capillary cfDNA and lactate values were taken in 23 professional football players before and after incremental exercise testing, during the course of a training week at rest (baseline) and in all 17 enrolled players following a season game. RESULTS: Lactate and venous cfDNA increased more pronounced during “short” compared to “long” (1.4-fold, p = 0.032 and 1.7-fold, p = 0.016) and cfDNA correlated significantly with lactate (r = 0.69; p<0.001). Incremental exercise testing increased cfDNA 7.0-fold (p<0.001). The season game increased cfDNA 22.7-fold (p<0.0001), while lactate showed a 2.0-fold (p = 0.09) increase compared to baseline. Fold-changes in cfDNA correlated with distance covered during game (spearman’s r = 0.87, p = 0.0012), while no correlation between lactate and the tracking data could be found. DISCUSSION: We show for the first time that cfDNA could be an objective marker for distance covered in elite intermittent sports. In contrast to the potential of more established blood-based markers like IL-6, CK, or CRP, cfDNA shows by far the strongest fold-change and a high correlation with a particular load related aspect in professional football. Public Library of Science 2018-01-25 /pmc/articles/PMC5784997/ /pubmed/29370268 http://dx.doi.org/10.1371/journal.pone.0191915 Text en © 2018 Haller 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
Haller, Nils
Helmig, Susanne
Taenny, Pascal
Petry, Julian
Schmidt, Sebastian
Simon, Perikles
Circulating, cell-free DNA as a marker for exercise load in intermittent sports
title Circulating, cell-free DNA as a marker for exercise load in intermittent sports
title_full Circulating, cell-free DNA as a marker for exercise load in intermittent sports
title_fullStr Circulating, cell-free DNA as a marker for exercise load in intermittent sports
title_full_unstemmed Circulating, cell-free DNA as a marker for exercise load in intermittent sports
title_short Circulating, cell-free DNA as a marker for exercise load in intermittent sports
title_sort circulating, cell-free dna as a marker for exercise load in intermittent sports
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5784997/
https://www.ncbi.nlm.nih.gov/pubmed/29370268
http://dx.doi.org/10.1371/journal.pone.0191915
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