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

被引:51
|
作者
Haller, Nils [1 ]
Helmig, Susanne [1 ]
Taenny, Pascal [1 ]
Petry, Julian [1 ]
Schmidt, Sebastian [1 ]
Simon, Perikles [1 ]
机构
[1] Johannes Gutenberg Univ Mainz, Dept Sports Med Rehabil & Prevent, Mainz, Germany
来源
PLOS ONE | 2018年 / 13卷 / 01期
关键词
FREE PLASMA DNA; MUSCLE DAMAGE; TIME-COURSE; OXIDATIVE STRESS; MAXIMAL EXERCISE; INFLAMMATION; FATIGUE; RELEASE; GENES; BLOOD;
D O I
10.1371/journal.pone.0191915
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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页数:12
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