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Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction
The prevalence of heart failure with preserved ejection fraction (HFpEF) is constantly increasing and no evidence-based pharmacological treatment option is available. While exercise training (ET) improves diastolic function, its metabolic mechanisms in HFpEF are unclear. We assessed the metabolic re...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572398/ https://www.ncbi.nlm.nih.gov/pubmed/31035733 http://dx.doi.org/10.3390/jcm8050591 |
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author | Bahls, Martin Friedrich, Nele Pietzner, Maik Wachter, Rolf Budde, Kathrin Hasenfuß, Gerd Nauck, Matthias Pressler, Axel Felix, Stephan B. Edelmann, Frank Halle, Martin Dörr, Marcus |
author_facet | Bahls, Martin Friedrich, Nele Pietzner, Maik Wachter, Rolf Budde, Kathrin Hasenfuß, Gerd Nauck, Matthias Pressler, Axel Felix, Stephan B. Edelmann, Frank Halle, Martin Dörr, Marcus |
author_sort | Bahls, Martin |
collection | PubMed |
description | The prevalence of heart failure with preserved ejection fraction (HFpEF) is constantly increasing and no evidence-based pharmacological treatment option is available. While exercise training (ET) improves diastolic function, its metabolic mechanisms in HFpEF are unclear. We assessed the metabolic response to 12 weeks of ET in patients with HFpEF by performing a post hoc analysis of the Ex-DHF-P trial (ISRCTN42524037). Plasma concentrations of 188 endogenous metabolites were measured in 44 ET and 20 usual care (UC) patients at baseline and 3-months follow-up. Metabolic differences between ET and UC from baseline to follow-up were compared and differential responses to ET were examined by random forest feature selection. ET prevented the increase of acetylornithine and carnitine as well as the decrease of three glycerophospholipids. After ET, two opposite metabolic response clusters were identified. Cluster belonging was associated with perceived well-being at baseline and changes in low-density lipoprotein but not with cardiorespiratory, ventilatory or echocardiographic parameters. These two ET-induced metabolic response patterns illustrate the heterogeneity of the HFpEF patient population. Our results suggest that other biological parameters might be helpful besides clinical variables to improve HFpEF patient stratification. Whether this approach improves response prediction regarding ET and other treatments should be explored. |
format | Online Article Text |
id | pubmed-6572398 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-65723982019-06-18 Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction Bahls, Martin Friedrich, Nele Pietzner, Maik Wachter, Rolf Budde, Kathrin Hasenfuß, Gerd Nauck, Matthias Pressler, Axel Felix, Stephan B. Edelmann, Frank Halle, Martin Dörr, Marcus J Clin Med Article The prevalence of heart failure with preserved ejection fraction (HFpEF) is constantly increasing and no evidence-based pharmacological treatment option is available. While exercise training (ET) improves diastolic function, its metabolic mechanisms in HFpEF are unclear. We assessed the metabolic response to 12 weeks of ET in patients with HFpEF by performing a post hoc analysis of the Ex-DHF-P trial (ISRCTN42524037). Plasma concentrations of 188 endogenous metabolites were measured in 44 ET and 20 usual care (UC) patients at baseline and 3-months follow-up. Metabolic differences between ET and UC from baseline to follow-up were compared and differential responses to ET were examined by random forest feature selection. ET prevented the increase of acetylornithine and carnitine as well as the decrease of three glycerophospholipids. After ET, two opposite metabolic response clusters were identified. Cluster belonging was associated with perceived well-being at baseline and changes in low-density lipoprotein but not with cardiorespiratory, ventilatory or echocardiographic parameters. These two ET-induced metabolic response patterns illustrate the heterogeneity of the HFpEF patient population. Our results suggest that other biological parameters might be helpful besides clinical variables to improve HFpEF patient stratification. Whether this approach improves response prediction regarding ET and other treatments should be explored. MDPI 2019-04-29 /pmc/articles/PMC6572398/ /pubmed/31035733 http://dx.doi.org/10.3390/jcm8050591 Text en © 2019 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Bahls, Martin Friedrich, Nele Pietzner, Maik Wachter, Rolf Budde, Kathrin Hasenfuß, Gerd Nauck, Matthias Pressler, Axel Felix, Stephan B. Edelmann, Frank Halle, Martin Dörr, Marcus Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction |
title | Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction |
title_full | Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction |
title_fullStr | Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction |
title_full_unstemmed | Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction |
title_short | Heterogeneous Metabolic Response to Exercise Training in Heart Failure with Preserved Ejection Fraction |
title_sort | heterogeneous metabolic response to exercise training in heart failure with preserved ejection fraction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6572398/ https://www.ncbi.nlm.nih.gov/pubmed/31035733 http://dx.doi.org/10.3390/jcm8050591 |
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