Tofts P S, Kermode A G
Multiple Sclerosis NMR Research Group, Institute of Neurology, London, United Kingdom.
Magn Reson Med. 1991 Feb;17(2):357-67. doi: 10.1002/mrm.1910170208.
Leakage of Gd-DTPA through a defective blood-brain barrier is measured quantitatively using dynamic MRI scanning, in which repeated scans are made after a bolus injection. Image registration artifacts are minimized; a dose of 0.1 mM/kg and an IR sequence enable enhancement to be measured quantitatively. The triexponential enhancement curve is fitted to a theoretical model based on compartmental analysis. The transfer constant, or permeability surface area product per unit volume of tissue (k), and leakage space per unit volume of tissue (v1) are measured. Estimates for a quickly enhancing multiple sclerosis lesion are k = 0.050 min-1, v1 = 21%; for a slow one k = 0.013 min-1, v1 = 49%. This implies permeability in the range 4-17 x 10(-6) cm s-1, in broad agreement with other physiological methods. The method is noninvasive and can be used to make serial measurements in patients and in experimental animal models. The time course of pathological aspects of diseases with blood-brain barrier breakdown, such as multiple sclerosis, tumors, and infections (e.g., HIV) can be studied, along with their response to therapy. The measurements are of physiological variables and are therefore independent of imaging equipment and field.
通过动态磁共振成像扫描定量测量钆喷酸葡胺透过有缺陷的血脑屏障的情况,在团注后进行多次重复扫描。图像配准伪影被降至最低;0.1 mM/kg的剂量和反转恢复(IR)序列能够对增强情况进行定量测量。将三指数增强曲线拟合到基于房室分析的理论模型。测量组织单位体积的转运常数或通透表面积乘积(k)以及组织单位体积的渗漏空间(v1)。快速强化的多发性硬化病灶的估计值为k = 0.050 min⁻¹,v1 = 21%;缓慢强化的病灶k = 0.013 min⁻¹,v1 = 49%。这意味着通透性在4 - 17×10⁻⁶ cm s⁻¹范围内,与其他生理学方法大致相符。该方法是非侵入性的,可用于对患者和实验动物模型进行系列测量。可以研究血脑屏障破坏的疾病(如多发性硬化、肿瘤和感染,例如艾滋病病毒感染)的病理过程及其对治疗的反应。这些测量是关于生理变量的,因此与成像设备和磁场无关。