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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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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. |
format | Online Article Text |
id | pubmed-5784997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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