1H-MR spectroscopy for analysis of cardiac lipid and creatine metabolism

被引:0
作者
Kiterie M. E. Faller
Craig A. Lygate
Stefan Neubauer
Jürgen E. Schneider
机构
[1] University of Oxford,Department of Cardiovascular Medicine, British Heart Foundation Experimental Magnetic Resonance Unit (BMRU), Wellcome Trust Centre for Human Genetics
来源
Heart Failure Reviews | 2013年 / 18卷
关键词
Heart; Metabolism; Magnetic resonance spectroscopy; ¹H-MRS; Creatine; Lipids;
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学科分类号
摘要
Magnetic resonance spectroscopy (MRS) is the only non-invasive, non-radiation-based technique for investigating the metabolism of living tissue. MRS of protons (1H-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 1H-MRS in humans and animal models of heart disease as detailed in this review.
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页码:657 / 668
页数:11
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共 494 条
[1]  
Neubauer S(2007)The failing heart–an engine out of fuel N Engl J Med 356 1140-1151
[2]  
Taegtmeyer H(1994)Energy metabolism of the heart: from basic concepts to clinical applications Curr Probl Cardiol 19 59-113
[3]  
Gupta A(2012)Creatine kinase-mediated improvement of function in failing mouse hearts provides causal evidence the failing heart is energy starved J Clin Invest 122 291-302
[4]  
Akki A(1988)Very rapid lactate measurement in ischemic perfused hearts using 1H MRS continuous negative echo acquisition during steady-state frequency selective excitation Magn Reson Med 7 65-78
[5]  
Wang Y(1993)Study of ischemic myocardial buffering capacity in perfused rat heart through rapidly interleaved 1H and 31P MRS measurements Magn Reson Med 30 115-119
[6]  
Leppo MK(1991)1H-nuclear magnetic resonance deoxymyoglobin signal as indicator of intracellular oxygenation in myocardium Am J Physiol 261 H2091-H2097
[7]  
Chacko VP(2001)Oxygen supply and oxidative phosphorylation limitation in rat myocardium in situ Am J Physiol Heart Circ Physiol 280 H2030-H2037
[8]  
Foster DB(1999)Myocardial oxygenation during high work states in hearts with postinfarction remodeling Circulation 99 942-948
[9]  
Caceres V(1999)Oxygen delivery does not limit cardiac performance during high work states Am J Physiol 277 H50-H57
[10]  
Shi S(1984)High resolution proton NMR studies of perfused rat hearts FEBS Lett 167 73-78