Novel cardiovascular biomarkers in patients with cardiovascular diseases undergoing intensive physical exercise.
Adult
Aged
Biomarkers
/ blood
Cardiac Rehabilitation
Coronary Artery Disease
/ blood
Enzyme-Linked Immunosorbent Assay
Exercise Therapy
Female
Germany
Growth Differentiation Factor 15
/ blood
Humans
Insulin-Like Growth Factor Binding Protein 2
/ blood
Interleukin-1 Receptor-Like 1 Protein
/ blood
Male
Middle Aged
Prospective Studies
Receptors, Urokinase Plasminogen Activator
/ blood
Time Factors
Treatment Outcome
Journal
Panminerva medica
ISSN: 1827-1898
Titre abrégé: Panminerva Med
Pays: Italy
ID NLM: 0421110
Informations de publication
Date de publication:
Sep 2020
Sep 2020
Historique:
pubmed:
21
4
2020
medline:
10
11
2021
entrez:
21
4
2020
Statut:
ppublish
Résumé
In this trial, we analyzed the plasma levels of novel biomarkers that reflect different pathophysiological pathways (sST2: mechanical strain, IGF-BP2: metabolic pathways, suPAR and GDF-15: inflammatory processes) in patients undergoing physical exercise to investigate the effects of training on their plasma concentrations. Plasma concentrations of novel biomarkers (sST2, IGF-BP2, suPAR and GDF-15) were analyzed by means of ELISA in patients with stable coronary artery disease (CAD) undergoing four weeks of high- and moderate-intensity training (EXCITE Trial) and in patients with one or more cardiovascular risk factors undergoing eight months of intensive physical exercise (IGF-BP2). Plasma levels of sST2 in patients undergoing eight months of intensive exercise have been published previously by our study group (1.13-fold change, P=0.045). Four weeks of high-intensity exercise training resulted in a statistically significant change in the plasma level of sST2 (1.106-fold change, P=0.0054) and IGF-BP2 (1.24-fold-change, P=0.0165). Eight months of intensive exercise resulted in a significant increase of IGF-BP2 (median 61.2 ng/mL to 80.7 ng/mL, 1.319-fold change, P=0.006). The significant increase of sST2 after four weeks might be a short-term effect due to the mechanical strain caused by the high-intensity training program, whereas the increase in IGF-BP2 after four weeks and eight months is likely a result of metabolic changes due to physical exercise.
Sections du résumé
BACKGROUND
BACKGROUND
In this trial, we analyzed the plasma levels of novel biomarkers that reflect different pathophysiological pathways (sST2: mechanical strain, IGF-BP2: metabolic pathways, suPAR and GDF-15: inflammatory processes) in patients undergoing physical exercise to investigate the effects of training on their plasma concentrations.
METHODS
METHODS
Plasma concentrations of novel biomarkers (sST2, IGF-BP2, suPAR and GDF-15) were analyzed by means of ELISA in patients with stable coronary artery disease (CAD) undergoing four weeks of high- and moderate-intensity training (EXCITE Trial) and in patients with one or more cardiovascular risk factors undergoing eight months of intensive physical exercise (IGF-BP2). Plasma levels of sST2 in patients undergoing eight months of intensive exercise have been published previously by our study group (1.13-fold change, P=0.045).
RESULTS
RESULTS
Four weeks of high-intensity exercise training resulted in a statistically significant change in the plasma level of sST2 (1.106-fold change, P=0.0054) and IGF-BP2 (1.24-fold-change, P=0.0165). Eight months of intensive exercise resulted in a significant increase of IGF-BP2 (median 61.2 ng/mL to 80.7 ng/mL, 1.319-fold change, P=0.006).
CONCLUSIONS
CONCLUSIONS
The significant increase of sST2 after four weeks might be a short-term effect due to the mechanical strain caused by the high-intensity training program, whereas the increase in IGF-BP2 after four weeks and eight months is likely a result of metabolic changes due to physical exercise.
Identifiants
pubmed: 32309918
pii: S0031-0808.20.03838-0
doi: 10.23736/S0031-0808.20.03838-0
doi:
Substances chimiques
Biomarkers
0
GDF15 protein, human
0
Growth Differentiation Factor 15
0
IGFBP2 protein, human
0
IL1RL1 protein, human
0
Insulin-Like Growth Factor Binding Protein 2
0
Interleukin-1 Receptor-Like 1 Protein
0
PLAUR protein, human
0
Receptors, Urokinase Plasminogen Activator
0
Types de publication
Comparative Study
Journal Article
Randomized Controlled Trial
Langues
eng
Sous-ensembles de citation
IM