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(1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism
Magnetic resonance spectroscopy (MRS) is the only non-invasive, non-radiation-based technique for investigating the metabolism of living tissue. MRS of protons ((1)H-MRS), which provides the highest sensitivity of all MR-visible nuclei, is a method capable of detecting and quantifying specific cardi...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782658/ https://www.ncbi.nlm.nih.gov/pubmed/22945240 http://dx.doi.org/10.1007/s10741-012-9341-z |
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author | Faller, Kiterie M. E. Lygate, Craig A. Neubauer, Stefan Schneider, Jürgen E. |
author_facet | Faller, Kiterie M. E. Lygate, Craig A. Neubauer, Stefan Schneider, Jürgen E. |
author_sort | Faller, Kiterie M. E. |
collection | PubMed |
description | Magnetic resonance spectroscopy (MRS) is the only non-invasive, non-radiation-based technique for investigating the metabolism of living tissue. MRS of protons ((1)H-MRS), which provides the highest sensitivity of all MR-visible nuclei, is a method capable of detecting and quantifying specific cardiac biomolecules, such as lipids and creatine in normal and diseased hearts in both animal models and humans. This can be used to study mechanisms of heart failure development in a longitudinal manner, for example, the potential contribution of myocardial lipid accumulation in the context of ageing and obesity. Similarly, quantifying creatine levels provides insight into the energy storage and buffering capacity in the heart. Creatine depletion is consistently observed in heart failure independent of aetiology, but its contribution to pathophysiology remains a matter of debate. These and other questions can in theory be answered with cardiac MRS, but fundamental technical challenges have limited its use. The metabolites studied with MRS are much lower concentration than water protons, requiring methods to suppress the dominant water signal and resulting in larger voxel sizes and longer scan times compared to MRI. However, recent technical advances in MR hardware and software have facilitated the application of (1)H-MRS in humans and animal models of heart disease as detailed in this review. |
format | Online Article Text |
id | pubmed-3782658 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-37826582013-09-25 (1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism Faller, Kiterie M. E. Lygate, Craig A. Neubauer, Stefan Schneider, Jürgen E. Heart Fail Rev Article Magnetic resonance spectroscopy (MRS) is the only non-invasive, non-radiation-based technique for investigating the metabolism of living tissue. MRS of protons ((1)H-MRS), which provides the highest sensitivity of all MR-visible nuclei, is a method capable of detecting and quantifying specific cardiac biomolecules, such as lipids and creatine in normal and diseased hearts in both animal models and humans. This can be used to study mechanisms of heart failure development in a longitudinal manner, for example, the potential contribution of myocardial lipid accumulation in the context of ageing and obesity. Similarly, quantifying creatine levels provides insight into the energy storage and buffering capacity in the heart. Creatine depletion is consistently observed in heart failure independent of aetiology, but its contribution to pathophysiology remains a matter of debate. These and other questions can in theory be answered with cardiac MRS, but fundamental technical challenges have limited its use. The metabolites studied with MRS are much lower concentration than water protons, requiring methods to suppress the dominant water signal and resulting in larger voxel sizes and longer scan times compared to MRI. However, recent technical advances in MR hardware and software have facilitated the application of (1)H-MRS in humans and animal models of heart disease as detailed in this review. Springer US 2012-09-04 2013 /pmc/articles/PMC3782658/ /pubmed/22945240 http://dx.doi.org/10.1007/s10741-012-9341-z Text en © The Author(s) 2012 https://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. |
spellingShingle | Article Faller, Kiterie M. E. Lygate, Craig A. Neubauer, Stefan Schneider, Jürgen E. (1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism |
title | (1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism |
title_full | (1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism |
title_fullStr | (1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism |
title_full_unstemmed | (1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism |
title_short | (1)H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism |
title_sort | (1)h-mr spectroscopy for analysis of cardiac lipid and creatine metabolism |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3782658/ https://www.ncbi.nlm.nih.gov/pubmed/22945240 http://dx.doi.org/10.1007/s10741-012-9341-z |
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