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

机译:1H-MR光谱分析心脏脂质和肌酸代谢

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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.
机译:磁共振波谱(MRS)是唯一用于研究活组织代谢的非侵入性,非辐射性技术。质子的MRS(1H-MRS)提供了所有MR可见核的最高灵敏度,是一种能够在动物模型和人类中检测和定量正常心脏和患病心脏中特定心脏生物分子(例如脂质和肌酸)的方法。这可用于纵向研究心力衰竭的机制,例如在衰老和肥胖的背景下心肌脂质蓄积的潜在作用。同样,定量肌酸水平可以深入了解心脏中的能量存储和缓冲能力。在心力衰竭中始终观察到肌酸耗竭,而与病因无关,但是肌酸耗竭对病理生理的影响仍是一个争论的问题。从理论上讲,这些问题和其他问题可以通过心脏MRS来解决,但是基本的技术挑战限制了其使用。与MRI相比,使用MRS研究的代谢物的浓度远低于水质子,因此需要抑制主要水信号的方法,并导致更大的体素大小和更长的扫描时间。但是,MR硬件和软件方面的最新技术进步促进了1H-MRS在心脏病的人和动物模型中的应用,如本文所详述。

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