基于磁共振成像的脑氧代谢量化技术的最新进展。

Felix W Wehrli
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摘要

氧代谢率(MRO2)是组织代谢的基础。测定 MRO2 需要了解血红蛋白结合氧浓度的动静脉差异(通常表示为氧萃取分数 (OEF))和血流速度 (BFR)。核磁共振成像是测量这两个量的独特方法,可以获得以 µmol O2 min-1/100 g 组织为绝对生理单位的 MRO2。本文讨论了两种方法,它们都依赖于血红蛋白磁性。重点是以脑 MRO2(CMRO2)表示的脑氧代谢,但也会涉及将相关技术转化到其他器官,包括肾脏和胎盘。第一类方法是利用血液的体磁感应强度,这可以从磁场图中得出。第二种方法基于对血水 T2 的测量,血水 T2 受红细胞内部和周围局部诱导场中的扩散和交换调制。一些全器官方法的时间分辨率足以对大脑能量进行时间序列研究,例如,在扫描仪中进行睡眠时,同时进行脑电图(EEG)睡眠阶段监测。与此相反,以时间分辨率换取空间分辨率的方法催生了基于定量血氧水平依赖性(BOLD)或校准 BOLD 模型的空间分辨率方法技术,从而可以对血管代谢参数进行区域评估,这两种方法也与全器官方法一样利用了脱氧血红蛋白的顺磁性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Recent Advances in MR Imaging-based Quantification of Brain Oxygen Metabolism.

The metabolic rate of oxygen (MRO2) is fundamental to tissue metabolism. Determination of MRO2 demands knowledge of the arterio-venous difference in hemoglobin-bound oxygen concentration, typically expressed as oxygen extraction fraction (OEF), and blood flow rate (BFR). MRI is uniquely suited for measurement of both these quantities, yielding MRO2 in absolute physiologic units of µmol O2 min-1/100 g tissue. Two approaches are discussed, both relying on hemoglobin magnetism. Emphasis will be on cerebral oxygen metabolism expressed in terms of the cerebral MRO2 (CMRO2), but translation of the relevant technologies to other organs, including kidney and placenta will be touched upon as well. The first class of methods exploits the blood's bulk magnetic susceptibility, which can be derived from field maps. The second is based on measurement of blood water T2, which is modulated by diffusion and exchange in the local-induced fields within and surrounding erythrocytes. Some whole-organ methods achieve temporal resolution adequate to permit time-series studies of brain energetics, for instance, during sleep in the scanner with concurrent electroencephalogram (EEG) sleep stage monitoring. Conversely, trading temporal for spatial resolution has led to techniques for spatially resolved approaches based on quantitative blood oxygen level dependent (BOLD) or calibrated BOLD models, allowing regional assessment of vascular-metabolic parameters, both also exploiting deoxyhemoglobin paramagnetism like their whole-organ counterparts.

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