The effect of exercise training on the course of cardiac troponin T and I levels: three independent training studies

Scientific Reports volume 5, Article number: 18320 (2016) Cite this article

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With the introduction of high-sensitive assays, cardiac troponins became potential biomarkers for risk stratification and prognostic medicine. Observational studies have reported an inverse association between physical activity and basal cardiac troponin levels. However, causality has never been demonstrated. This study investigated whether basal cardiac troponin concentrations are receptive to lifestyle interventions such as exercise training. Basal high-sensitive cardiac troponin T (cTnT ) and I (cTnI) were monitored in two resistance-type exercise training programs (12-week (study 1) and 24-week (study 2)) in older adults (≥65 years). In addition, a retrospective analysis for high sensitive troponin I in a 24-week exercise controlled trial in (pre)frail older adults was performed (study 3). In total, 91 subjects were included in the final data analyses. There were no significant changes in cardiac troponin levels over time in study 1 and 2 (study 1: cTnT −0.13 (−0.33–+0.08) ng/L/12-weeks, cTnI −0.10 (−0.33–+0.12) ng/L/12-weeks; study 2: cTnT −1.99 (−4.79–+0.81) ng/L/24-weeks, cTnI −1.59 (−5.70–+2.51) ng/L/24-weeks). Neither was there a significant interaction between training and the course of cardiac troponin in study 3 (p = 0.27). In conclusion, this study provides no evidence that prolonged resistance-type exercise training can modulate basal cardiac troponin levels.

The development of increasingly sensitive assays for cardiac troponin has now reached the point where cardiac troponin concentrations can be accurately assessed in the majority of subjects from a healthy reference population1. Parallel to the development of assays with increasing sensitivity, interest in cardiac troponin has expanded from acute cardiac care to risk prediction and risk stratification2. Studies in various patient groups and asymptomatic individuals have provided compelling evidence that baseline cardiac troponin levels predict outcome3. Interestingly, the observed risk gradient is not restricted to elevations above the 99th percentile, but is even apparent within the "healthy" population reference interval and independent of traditional risk factors such as age, sex and diabetes4,5,6,7,8,9. In the Framingham heart study, the basal cardiac troponin I concentration adds prognostic value to standard risk factors for predicting death and cardiovascular disease10. Furthermore, temporal increases in cardiac troponin concentrations over time confer additional cardiovascular risk and are inversely related to the level of physical fitness7,11. These observations form the basis of the hypothesis that cardiac troponin is a modifiable parameter, which may be receptive to lifestyle interventions such as an exercise training program. In a recent study with (pre)frail subjects we tested the hypothesis that a supervised resistance-type exercise training program can influence the course of cardiac troponin levels over time12. However, this 24-week supervised bi-weekly exercise training program conferred no beneficial effect on the course of cardiac troponin T levels, despite substantial improvements of these subjects at the level of physical performance12. This negative study was conducted in frail and pre-frail subjects, characterized by substantially elevated baseline cardiac troponin levels and therefore theoretically most amenable to the potential benefits of an exercise intervention. A possible drawback however, was the limited training load that could be imposed due to the level of frailty of these older subjects. Nevertheless, despite these limitations, our results were similar to those of other recent reports: 14-week endurance training in untrained adults13, 17-week half-marathon training in previously sedentary men14 and 3-month exercise training in heart failure patients (NYHA class II-IV)15 did not result reduce basal cardiac troponin T concentrations. However, limitations of these studies were the low basal cardiac troponin concentrations13 and the use of conventional instead of high-sensitive cardiac troponin T assays14,15 which reduced the power to detect an effect. Another issue that merits attention is that the effect of training intervention on cardiac troponin I has never been assessed. Since cardiac troponin T and I are two different proteins of the cardiac troponin complex with different biochemical characteristics16 and distinct release patterns17, both cardiac troponins may also respond differently to lifestyle interventions.

The aim of the current study is 1) to overcome the limitations of previous studies and 2) to examine the effect of exercise training on basal cardiac troponin I levels. Therefore, we now present two additional exercise training studies to the effect of a more intense training regimen on the course of high-sensitive cardiac troponin T and I levels in older adults, a population that often exhibits elevated basal cardiac troponin concentrations. Additional high sensitive troponin I was measured in our previously conducted study in (pre)frail subjects in order to present a complete and comprehensive overview to the effects of three supervised training programs.

To investigate the effect of resistance-type exercise training on cardiac troponin T (cTnT) and I (cTnI) in older adults, two independent studies were conducted: a study to the effect of 12-week resistance-type exercise training in older men (≥65 years) (study 1) and a second study to the effect of a 24-week resistance-type exercise training older men and women (≥65 years) (study 2). In addition, we performed a retrospective analysis for cardiac troponin I in our recently published study to the effect of a 24-week resistance-type exercise training program on the course of troponin T levels in (pre)frail subjects (≥65 years) (study 3).

All studies complied with the principles of the Declaration of Helsinki and were approved by the local institutional review boards and the ethics committees of Wageningen University or Maastricht University Medical Center. Participants were recruited by advertisements in local newspapers (study 1 and 2) or by approaching elderly living in apartment houses and in homes for the elderly (study 3). All participants provided written informed consent. Subjects were only eligible for inclusion when they had not participated in any structured exercise training program over the past 2 years.

In total 14 subjects were included in study 1. Inclusion criteria were age (65–85 years), male gender and the ability to understand and perform study procedures. Exclusion criteria were (silent) cardiac or peripheral vascular disease, orthopedic limitations (self-reported) and type 2 diabetes (based on an oral glucose tolerance test). A training session consisted of a 5-minute warming up on a cycle ergometer, four sets on leg-press and leg-extension machines and a 5-minute cooling down on the cycle ergometer. The workload started at 60% of 1 repetition maximum (1-RM) (10–15 repetitions per set) and was increased to 75–80% of 1-RM (8–10 repetitions per set). The typical duration of a training session was approximately 45 minutes and the work:rest ratio was 1:4. This supervised resistance-type exercise training program was performed three times per week during 12 weeks. There was at least a resting period of 2 days between consecutive training sessions. Blood samples were obtained by a venipuncture after an overnight fast, at least three days after the last training session, before the start of the training program (week 0) and after 4, 8 and 12 weeks of intervention. This study is a substudy of a more extensive trial examining the effects of resistance-type exercise training in older men on muscle strength, body composition and muscle fiber type-specific characteristics as primary outcome18.

In total 27 subjects were included in study 2. Inclusion criteria were age (65–90 years) and the ability to understand and perform study procedures. Exclusion criteria were the same as in study 1. Training sessions consisted of a 5-minute warming up on a cycle ergometer, four sets on leg-press and leg-extension machines and three sets on the chest press and horizontal row; these four exercises were performed every training session. In addition, three sets of vertical lat pull and abdominal crunches were alternated with biceps curl and triceps extension between subsequent training sessions. The workload started at 60% of 1-RM (10–15 repetitions per set) and was increased to 75–80% of 1-RM (8–10 repetitions per set). The typical duration of a training session was approximately 45 minutes and the work:rest ratio was 1:4. This supervised resistance-type exercise training program was performed three times per week during 24 weeks. There was at least a resting period of 2 days between consecutive training sessions. Blood samples were obtained by a venipuncture after an overnight fast at least three days after the last training session before the start of the training program (week 0) and after 4, 8, 12, 16, 20 and 24 weeks of intervention. This is a substudy of a more extensive trial to the effects of an exercise training intervention in older adults on muscle strength, body composition and muscle fiber type-specific characteristics. In this current study we included only subjects from the control group who were not receiving dietary protein supplementation (as described in the original study protocol)19,20.

Methodological details of study 3 have been described previously12. Briefly, a total of 62 (pre)frail older men and women (≥65 years) were included and were equally distributed in an intervention and a control group. Frailty and prefrailty were defined according to the Fried criteria (subjects were considered prefrail when 1 or 2 criteria were applicable and frail when 3 or more criteria were present): (1) unintentional weight loss, (2) weakness, (3) self-reported exhaustion, (4) slow walking speed and (5) low physical activity21. The intervention group participated in a 24-week, biweekly, supervised resistance-type exercise training program. Blood samples were obtained by a venipuncture after an overnight fast before the start of the training program (week 0), after 12 and after 24 weeks of intervention. The effect of the training program on muscle mass, muscle strength, physical performance and troponin T levels were published recently. In this current study we included only subjects from the control group who were not receiving dietary protein supplementation (as described in the original study protocol)12,22,23.

Plasma and serum samples were stored at −80 °C until analysis. Serum (study 1) and plasma (study 2 and 3) cardiac troponins were measured using the high sensitive cTnT assay (limit of blank 3.0 ng/L, limit of detection 5.0 ng/L, 99th percentile 14 ng/L24) on the Cobas analyzer (Roche Diagnostics) and the high sensitive cTnI assay (according to the manufacturer, limit of blank 0.7–1.3 ng/L, limit of detection 1.1–1.9 ng/L, 99th percentile 26.2 ng/L and 10% CV 4.7 ng/L) on the ARCHITECT analyzer (Abbott Diagnostics).

Normally distributed parameters were expressed as mean ± standard deviation (SD), non-normally distributed parameters as median and interquartile range (IQR) and categorical variables as number (n) and percentage (%). Changes in basal cardiac troponin T and I concentrations over time were analyzed using mixed linear model analyses (random intercept) with the covariate time as fixed effect. The inclusion of 14 subjects in study 1 and 27 subjects in study 2 afforded at least 90% power at a significance level of 5% to detect a 10% reduction in cardiac troponin levels, anticipating a dropout rate of 25%. These post-hoc power calculations were based on the assumption of a mean baseline cTnT concentration of 8.0 ng/L and cTnI concentration of 6.0 ng/L for study 1 and a mean baseline cardiac cTnT concentration of 6.0 ng/L and a cTnI concentration of 4.0 ng/L for study 2 with older men and women (estimated baseline correlation and decay rate 0.90 and 0.25, respectively)25. We used two-level design mixed linear model analyses (random intercept) with time and intervention as fixed effects to assess the differences in the course of cardiac troponin I between (pre)frail subjects in the control group and in the intervention group. Power calculation for study 3 has been described previously12. All statistical analyses were performed using SPSS, version 20.0. P ≤ 0.05 was considered statistically significant for all analyses.

Included subjects in study 1 and 2 demonstrated 97% and 90% compliance, respectively, to the scheduled, supervised training sessions. In each study one subject withdrew. Ten subjects (15%) withdrew from study 3. Subjects withdrew because of time constraints and medical reasons unrelated to the exercise training. In total, in the final data analysis we included: 13 older men participating in the 12-week training program (study 1), 26 older men and women participating in the 24-week training program (study 2) and 52 subjects in the retrospective troponin I analysis with (pre)frail older men and women (study 3). Table 1 shows the subjects’ clinical characteristics at baseline. Baseline characteristics for the (pre)frail subjects have been published previously12.

Figure 1 shows the course of cardiac troponin T and cardiac troponin I levels over time in study 1 and 2 (for individual data see Supplementary Fig. S1 and S2 online). Table 2 shows the corresponding baseline and the follow-up values for cTnT and cTnI. One subject in study 2 (3% of the participants in study 1 and 2) had cardiac troponin T concentrations below the limit of blank (3ng/L) at all time points and was therefore excluded from the cardiac troponin T analysis. In study 1 and 2 98.6% and 99.6% of all other troponin T and I measurements respectively had concentrations above the limit of blank. Using mixed linear model analyses, we found no significant changes in cardiac troponin levels over time in older men participating in a 12-week resistance-type exercise training program (cTnT −0.13 (−0.33–+0.08) ng/L/12-weeks (p = 0.16), cTnI −0.10 (−0.33–+0.12) ng/L/12-weeks (p = 0.44)) and in older men and women participating in a 24-week resistance-type exercise training program (cTnT −1.99 (−4.79–+0.81) ng/L/24-weeks (p = 0.23), cTnI −1.59 (−5.70–+2.51) ng/L/24-weeks (p = 0.37)).

Course of cardiac troponinT and I in older adults participating in 12- and 24-week training programs.

Median (interquartile range) concentrations of cTn in older adults participating in a supervised resistance-type training program: (A) course of cTnT in older men in a 12-week training program; (B) course of cTnI in older men in a 12-week training program; (C) course of cTnT in older men and women in a 24-week training program; (D) course of cTnI in older men and women in a 24-week training program.

Table 3 shows the baseline cTnI concentrations and the 12-week and 24-week follow-up data of (pre)frail older men and women. In the control group, all values were above the limit of blank of the assay (1.3 ng/L), 3 subjects had at least one value above the 99th percentile of 26.2 ng/L, which is used for the diagnosis of myocardial infarction. In the intervention group, one subject had one value below limit of blank of the assay and one subject had at least one value above the 99th percentile. Mixed linear model analyses revealed no significant interaction between training and the course of cTnI levels between the intervention and the control group (intention-to-treat analysis p = 0.27, per-protocol analysis p = 0.27) (for individual data see Supplementary Fig. S2 online).

In two independent supervised training studies of 12 and 24 weeks respectively, we found no effect of resistance-type exercise training on the course of cardiac troponin T and I levels in older subjects, nor did we find an effect of a 24-week training program on cardiac troponin I levels in (pre)frail subjects.

Our results do not support the idea that cardiac troponin levels might be modifiable through exercise. This hypothesis was postulated by observational studies, showing that higher physical activity levels in older subjects were associated with both lower basal cTnT levels and a lower probability of a significant increase in cTnT concentrations between consecutive visits11,26. To investigate whether a causal relationship underlies this association, we conducted a series of training studies in subjects where stable elevated cardiac troponin levels are common and who are therefore -at least theoretically- most receptive to the favorable effects of an intervention. To ensure that basal cardiac troponin levels, rather than acute post-exercise effects were studied, we included a three day interval between the last training session and the blood sampling procedure27. None of these studies showed a favorable effect of resistance-type exercise training on cardiac troponin levels. The non-responsive pattern of troponin T and I to an exercise program is in contrast with the beneficial changes observed for leg strength, muscle mass, insulin sensitivity, HbA1c, total cholesterol and LDL18,19,20,22,23. The present results confirm and extend the results of our previous training intervention study in (pre)frail older adults12, which was also characterized by favorable effects on physical performance, but a lack of effect on circulating cardiac troponin levels.

Although the absolute number of subjects in these training studies are relatively low, all studies afforded at least 90% power to detect a 10% reduction of cardiac troponin over time. We cannot exclude the possibility that training confers a smaller effect on the course of troponin levels that goes by undetected in the present study, but we feel that (much) smaller changes than specified in our power calculation would comprise limited clinical relevance. A possible limitation of our study relates to the type of exercise training intervention, comprising mostly resistance-type exercise. However the subjects’ physical state precluded (intense) endurance training. Despite the physical and metabolic improvements found in our studies18,19,20,22,23, a valid question may be whether resistance-type exercise training is the most appropriate type of training to generate a favorable effect on cardiac troponin concentrations. In this respect the results of a recently conducted cardio-based exercise training intervention study in heart failure patients are interesting. Similar to our studies, no favorable effect was found of a supervised endurance exercise training program on cardiac troponin T levels15.

The supervision during the sessions contributed to the internal validity, but might also have led to increased safety, less adverse events and a higher motivation among subjects. This may overestimate any beneficial effects of exercise training. Another point regarding the validity of our study is the participant recruitment process and study design. Since participation in the study is associated with a substantial time investment and a relatively high intensity training program, this might have attracted a specific, highly motivated subpopulation. Since our study was conducted in an elderly population we can only speculate about the effects of exercise training on basal cardiac troponin levels in younger subjects who may respond differently on exercise training and demonstrate higher cardiovascular plasticity28. Nevertheless, our study does not provide support for the hypothesis that basal cardiac troponin concentrations are receptive to a prolonged resistance-type exercise training program.

How to cite this article: van der Linden, N. et al. The effect of exercise training on the course of cardiac troponin T and I levels: three independent training studies. Sci. Rep. 5, 18320; doi: 10.1038/srep18320 (2015).

Koerbin, G. et al. Characterisation of a highly sensitive troponin I assay and its application to a cardio-healthy population. Clinical chemistry and laboratory medicine: CCLM/FESCC 50, 871–878, doi: 10.1515/cclm-2011-0540 (2012).

Article CAS Google Scholar

Giannitsis, E. & Katus, H. A. Highly sensitive troponins knocking at the door of primary prevention. European heart journal 35, 268–270, doi: 10.1093/eurheartj/eht479 (2014).

Article PubMed Google Scholar

Mills, N. L. et al. Implementation of a sensitive troponin I assay and risk of recurrent myocardial infarction and death in patients with suspected acute coronary syndrome. JAMA: the journal of the American Medical Association 305, 1210–1216, doi: 10.1001/jama.2011.338 (2011).

Article CAS PubMed Google Scholar

de Lemos, J. A. et al. Association of troponin T detected with a highly sensitive assay and cardiac structure and mortality risk in the general population. Jama 304, 2503–2512, doi: 10.1001/jama.2010.1768 (2010).

Article CAS PubMed PubMed Central Google Scholar

Saunders, J. T. et al. Cardiac troponin T measured by a highly sensitive assay predicts coronary heart disease, heart failure and mortality in the Atherosclerosis Risk in Communities Study. Circulation 123, 1367–1376, doi: 10.1161/CIRCULATIONAHA.110.005264 (2011).

Article CAS PubMed PubMed Central Google Scholar

Zeller, T. et al. High population prevalence of cardiac troponin I measured by a high-sensitivity assay and cardiovascular risk estimation: the MORGAM Biomarker Project Scottish Cohort. European heart journal 35, 271–281, doi: 10.1093/eurheartj/eht406 (2014).

Article CAS PubMed Google Scholar

Eggers, K. M., Venge, P., Lindahl, B. & Lind, L. Cardiac troponin I levels measured with a high-sensitive assay increase over time and are strong predictors of mortality in an elderly population. Journal of the American College of Cardiology 61, 1906–1913, doi: 10.1016/j.jacc.2012.12.048 (2013).

Article CAS PubMed Google Scholar

White, H. D. et al. Association of contemporary sensitive troponin I levels at baseline and change at 1 year with long-term coronary events following myocardial infarction or unstable angina: results from the LIPID Study (Long-Term Intervention With Pravastatin in Ischaemic Disease). Journal of the American College of Cardiology 63, 345–354, doi: 10.1016/j.jacc.2013.08.1643 (2014).

Article CAS PubMed Google Scholar

Collinson, P. The role of cardiac biomarkers in cardiovascular disease risk assessment. Current opinion in cardiology, doi: 10.1097/HCO.0000000000000081 (2014).

Wang, T. J. et al. Prognostic utility of novel biomarkers of cardiovascular stress: the Framingham Heart Study. Circulation 126, 1596–1604, doi: 10.1161/CIRCULATIONAHA.112.129437 (2012).

Article CAS PubMed Google Scholar

deFilippi, C. R. et al. Physical activity, change in biomarkers of myocardial stress and injury and subsequent heart failure risk in older adults. Journal of the American College of Cardiology 60, 2539–2547, doi: 10.1016/j.jacc.2012.08.1006 (2012).

Article CAS PubMed PubMed Central Google Scholar

van der Linden, N. et al. The effect of a six-month resistance-type exercise training program on the course of high sensitive cardiac troponin T levels in (pre)frail elderly. International journal of cardiology 175, 374–375, doi: 10.1016/j.ijcard.2014.05.017 (2014).

Article CAS PubMed Google Scholar

Legaz-Arrese, A. et al. Impact of an endurance training program on exercise-induced cardiac biomarker release. Am J Physiol Heart Circ Physiol 308, H913–920, doi: 10.1152/ajpheart.00914.2014 (2015).

Article CAS PubMed Google Scholar

Vance, D. D. et al. Cardiac performance, biomarkers and gene expression studies in previously sedentary men participating in half-marathon training. BMC sports science, medicine and rehabilitation 6, 6, doi: 10.1186/2052-1847-6-6 (2014).

Article PubMed PubMed Central Google Scholar

Ahmad, T. et al. The effects of exercise on cardiovascular biomarkers in patients with chronic heart failure. American heart journal 167, 193–202 e191, doi: 10.1016/j.ahj.2013.10.018 (2014).

Article CAS Google Scholar

Katrukha, I. A. Human cardiac troponin complex. Structure and functions. Biochemistry (Mosc) 78, 1447–1465, doi: 10.1134/S0006297913130063 (2013).

Article CAS Google Scholar

Agewall, S., Giannitsis, E., Jernberg, T. & Katus, H. Troponin elevation in coronary vs. non-coronary disease. European heart journal 32, 404–411, doi: 10.1093/eurheartj/ehq456 (2011).

Article CAS PubMed Google Scholar

Verdijk, L. B. et al. Skeletal muscle hypertrophy following resistance training is accompanied by a fiber type-specific increase in satellite cell content in elderly men. The journals of gerontology. Series A, Biological sciences and medical sciences 64, 332–339, doi: 10.1093/gerona/gln050 (2009).

Article CAS Google Scholar

Leenders, M. et al. Elderly men and women benefit equally from prolonged resistance-type exercise training. The journals of gerontology. Series A, Biological sciences and medical sciences 68, 769–779, doi: 10.1093/gerona/gls241 (2013).

Article Google Scholar

Leenders, M. et al. Protein supplementation during resistance-type exercise training in the elderly. Medicine and science in sports and exercise 45, 542–552, doi: 10.1249/MSS.0b013e318272fcdb (2013).

Article CAS PubMed Google Scholar

Fried, L. P. et al. Frailty in older adults: evidence for a phenotype. The journals of gerontology. Series A, Biological sciences and medical sciences 56, M146–156 (2001).

Article CAS Google Scholar

Tieland, M. et al. Protein supplementation increases muscle mass gain during prolonged resistance-type exercise training in frail elderly people: a randomized, double-blind, placebo-controlled trial. Journal of the American Medical Directors Association 13, 713–719, doi: 10.1016/j.jamda.2012.05.020 (2012).

Article PubMed Google Scholar

Tieland, M. et al. Protein supplementation improves physical performance in frail elderly people: a randomized, double-blind, placebo-controlled trial. Journal of the American Medical Directors Association 13, 720–726, doi: 10.1016/j.jamda.2012.07.005 (2012).

Article PubMed Google Scholar

Giannitsis, E. et al. Analytical validation of a high-sensitivity cardiac troponin T assay. Clinical chemistry 56, 254–261, doi: 10.1373/clinchem.2009.132654 (2010).

Article CAS PubMed Google Scholar

Guo, Y., Logan, H. L., Glueck, D. H. & Muller, K. E. Selecting a sample size for studies with repeated measures. BMC medical research methodology 13, 100, doi: 10.1186/1471-2288-13-100 (2013).

Article PubMed PubMed Central Google Scholar

Klenk, J. et al. Association of objectively measured physical activity with established and novel cardiovascular biomarkers in elderly subjects: every step counts. Journal of epidemiology and community health 67, 194–197, doi: 10.1136/jech-2012-201312 (2013).

Article PubMed Google Scholar

Savukoski, T., Mehtala, L., Lindahl, B., Venge, P. & Pettersson, K. Elevation of cardiac troponins measured after recreational resistance training. Clin Biochem, doi: 10.1016/j.clinbiochem.2015.06.015 (2015).

Wang, E. et al. Exercise-training-induced changes in metabolic capacity with age: the role of central cardiovascular plasticity. Age (Dordr) 36, 665–676, doi: 10.1007/s11357-013-9596-x (2014).

Article CAS Google Scholar

Inker, L. A. et al. Estimating glomerular filtration rate from serum creatinine and cystatin C. The New England journal of medicine 367, 20–29, doi: 10.1056/NEJMoa1114248 (2012).

Article CAS PubMed PubMed Central Google Scholar

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Department of Clinical Chemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University Medical Center (MUMC), Maastricht, The Netherlands

Noreen van der Linden, Lieke J. J. Klinkenberg, Otto Bekers, Marja P. van Dieijen-Visser & Steven J. R. Meex

Department of Human Movement Sciences, School for Nutrition, Toxicology and Metabolism (NUTRIM), Maastricht University Medical Center (MUMC), Maastricht, The Netherlands

Marika Leenders, Lex B. Verdijk & Luc J. C. van Loon

Top Institute Food and Nutrition, Wageningen University, Wageningen, The Netherlands

Marika Leenders, Michael Tieland, Lex B. Verdijk, Lisette C. P. G. M. de Groot & Luc J. C. van Loon

Division of Human Nutrition, Wageningen University, Wageningen, The Netherlands

Michael Tieland & Lisette C. P. G. M. de Groot

Department of Clinical Chemistry, Gelre Ziekenhuizen, Apeldoorn, The Netherlands

Marijke Niens & Jeroen D. E. van Suijlen

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N.v.d.L., L.d.G., L.v.L., M.v.D.-V. and S.M. conceived the experiments, N.v.d.L., L.K., M.L., M.T., L.V. and M.N. conducted the experiments, N.v.d.L., L.K. and S.M. analysed the results and N.v.d.L. and S.M. drafted the manuscript. N.v.d.L., L.K., M.L., M.T., L.V., M.N., J.v.S., L.d.G., O.B., L.v.L., M.v.D.-V. and S.M. reviewed the manuscript.

The authors declare no competing financial interests.

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van der Linden, N., Klinkenberg, L., Leenders, M. et al. The effect of exercise training on the course of cardiac troponin T and I levels: three independent training studies. Sci Rep 5, 18320 (2016). https://doi.org/10.1038/srep18320

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Received: 17 June 2015

Accepted: 16 November 2015

Published: 16 December 2015

DOI: https://doi.org/10.1038/srep18320

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The effect of exercise training on the course of cardiac troponin T and I levels: three independent training studies