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Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart

BACKGROUND: Heart failure patients have inadequate nutritional intake and alterations in metabolism contributing to an overall energy depleted state. Left ventricular assist device (LVAD) support is a common and successful intervention in patients with end-stage heart failure. LVAD support leads to...

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Autores principales: Weitzel, Lindsay B., Ambardekar, Amrut V., Brieke, Andreas, Cleveland, Joseph C., Serkova, Natalie J., Wischmeyer, Paul E., Lowes, Brian D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613395/
https://www.ncbi.nlm.nih.gov/pubmed/23560088
http://dx.doi.org/10.1371/journal.pone.0060292
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author Weitzel, Lindsay B.
Ambardekar, Amrut V.
Brieke, Andreas
Cleveland, Joseph C.
Serkova, Natalie J.
Wischmeyer, Paul E.
Lowes, Brian D.
author_facet Weitzel, Lindsay B.
Ambardekar, Amrut V.
Brieke, Andreas
Cleveland, Joseph C.
Serkova, Natalie J.
Wischmeyer, Paul E.
Lowes, Brian D.
author_sort Weitzel, Lindsay B.
collection PubMed
description BACKGROUND: Heart failure patients have inadequate nutritional intake and alterations in metabolism contributing to an overall energy depleted state. Left ventricular assist device (LVAD) support is a common and successful intervention in patients with end-stage heart failure. LVAD support leads to alterations in cardiac output, functional status, neurohormonal activity and transcriptional profiles but the effects of LVADs on myocardial metabolism are unknown. This study set out to measure cardiac metabolites in non-failing hearts, failing hearts, and hearts post-LVAD support. METHODS: The study population consisted of 8 non-ischemic failing (at LVAD implant) and 8 post-LVAD hearts, plus 8 non-failing hearts obtained from the tissue bank at the University of Colorado. NMR spectroscopy was utilized to evaluate differences in myocardial energy substrates. Paired and non-paired t-tests were used to determine differences between the appropriate groups. RESULTS: Glucose and lactate values both decreased from non-failing to failing hearts and increased again significantly in the (paired) post-LVAD hearts. Glutamine, alanine, and aromatic amino acids decreased from non-failing to failing hearts and did not change significantly post-LVAD. Total creatine and succinate decreased from non-failing to failing hearts and did not change significantly post-LVAD. DISCUSSION: Measured metabolites related to glucose metabolism are diminished in failing hearts, but recovered their values post-LVAD. This differed from the amino acid levels, which decreased in heart failure but did not recover following LVAD. Creatine and the citric acid cycle intermediate succinate followed a similar pattern as the amino acid levels.
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spelling pubmed-36133952013-04-04 Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart Weitzel, Lindsay B. Ambardekar, Amrut V. Brieke, Andreas Cleveland, Joseph C. Serkova, Natalie J. Wischmeyer, Paul E. Lowes, Brian D. PLoS One Research Article BACKGROUND: Heart failure patients have inadequate nutritional intake and alterations in metabolism contributing to an overall energy depleted state. Left ventricular assist device (LVAD) support is a common and successful intervention in patients with end-stage heart failure. LVAD support leads to alterations in cardiac output, functional status, neurohormonal activity and transcriptional profiles but the effects of LVADs on myocardial metabolism are unknown. This study set out to measure cardiac metabolites in non-failing hearts, failing hearts, and hearts post-LVAD support. METHODS: The study population consisted of 8 non-ischemic failing (at LVAD implant) and 8 post-LVAD hearts, plus 8 non-failing hearts obtained from the tissue bank at the University of Colorado. NMR spectroscopy was utilized to evaluate differences in myocardial energy substrates. Paired and non-paired t-tests were used to determine differences between the appropriate groups. RESULTS: Glucose and lactate values both decreased from non-failing to failing hearts and increased again significantly in the (paired) post-LVAD hearts. Glutamine, alanine, and aromatic amino acids decreased from non-failing to failing hearts and did not change significantly post-LVAD. Total creatine and succinate decreased from non-failing to failing hearts and did not change significantly post-LVAD. DISCUSSION: Measured metabolites related to glucose metabolism are diminished in failing hearts, but recovered their values post-LVAD. This differed from the amino acid levels, which decreased in heart failure but did not recover following LVAD. Creatine and the citric acid cycle intermediate succinate followed a similar pattern as the amino acid levels. Public Library of Science 2013-04-01 /pmc/articles/PMC3613395/ /pubmed/23560088 http://dx.doi.org/10.1371/journal.pone.0060292 Text en © 2013 Weitzel 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Weitzel, Lindsay B.
Ambardekar, Amrut V.
Brieke, Andreas
Cleveland, Joseph C.
Serkova, Natalie J.
Wischmeyer, Paul E.
Lowes, Brian D.
Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart
title Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart
title_full Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart
title_fullStr Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart
title_full_unstemmed Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart
title_short Left Ventricular Assist Device Effects on Metabolic Substrates in the Failing Heart
title_sort left ventricular assist device effects on metabolic substrates in the failing heart
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3613395/
https://www.ncbi.nlm.nih.gov/pubmed/23560088
http://dx.doi.org/10.1371/journal.pone.0060292
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