Taheri Saeid, Rosenberg Gary A, Ford Corey
Department of Radiology and Radiological Sciences, MSC 323, Medical University of South Carolina, Charleston, SC 29425-3230, United States.
Department of Neurology, Departments of Neurosciences, and Cell Biology and Physiology, University of New Mexico Health Sciences Center, Albuquerque, NM 87107, United States.
Mult Scler Relat Disord. 2013 Apr;2(2):124-32. doi: 10.1016/j.msard.2012.09.003. Epub 2012 Oct 24.
Blood-brain barrier (BBB) disruption visualized in lesions by MRI is a major biomarker of disease activity in multiple sclerosis (MS). However, in MS, destruction occurs to a variable extent in lesions as well as in gray matter (GM) and in the normal appearing white matter (NAWM). A method to quantify the BBB disruption in lesions as well as in non-lesion areas would be useful for assessment of MS progression and treatments. The objective of this study was to quantify the BBB transfer rate (Ki) in WM lesions, in the NAWM, and in the full-brain of MS patients. Thirteen MS patients with active lesions and 10 healthy controls with age and gender matching were recruited for full-brain and WM Ki studies. Dynamic contrast-enhanced MRI (DCEMRI) scans were conducted using T1 mapping with partial inversion recovery (TAPIR), a fast T1 mapping technique, following administration of a quarter-dose of the contrast agent Gadolinium-DTPA (Gd-DTPA). The Patlak modeling technique was used to derive a voxel-based map of Ki. In all patients contrast-enhanced lesions, quantified by Ki maps, were observed. Compared with controls, patients with MS exhibited an increase in mean Ki of the full-brain (P-value<0.05) but no significant difference in mean Ki of NAWM. The identified increase in full-brain Ki of MS patients suggests a global vascular involvement associated with MS disease. The lack of observed significant decrease in Ki in NAWM suggests lower involvement of WM vasculature than full-brain vasculature in MS. Ki maps constructed from time series data acquired by DCEMRI provide additional information about BBB that could be used for evaluation of vascular involvement in MS and monitoring treatment effectiveness.
磁共振成像(MRI)显示的病变中血脑屏障(BBB)破坏是多发性硬化症(MS)疾病活动的主要生物标志物。然而,在MS中,病变以及灰质(GM)和正常外观白质(NAWM)中均会发生不同程度的破坏。一种量化病变以及非病变区域中BBB破坏的方法对于评估MS进展和治疗将是有用的。本研究的目的是量化MS患者白质病变、NAWM和全脑中的BBB转移率(Ki)。招募了13名有活动性病变的MS患者和10名年龄和性别匹配的健康对照进行全脑和白质Ki研究。在给予四分之一剂量的造影剂钆喷酸葡胺(Gd-DTPA)后,使用快速T1映射技术部分反转恢复(TAPIR)进行T1映射的动态对比增强MRI(DCEMRI)扫描。采用Patlak建模技术得出基于体素的Ki图。在所有患者中均观察到通过Ki图量化的对比增强病变。与对照组相比,MS患者全脑的平均Ki增加(P值<0.05),但NAWM的平均Ki无显著差异。MS患者全脑Ki的增加表明与MS疾病相关的全身性血管受累。在NAWM中未观察到Ki显著降低,这表明在MS中白质血管系统的受累程度低于全脑血管系统。由DCEMRI获取的时间序列数据构建的Ki图提供了有关BBB的额外信息,可用于评估MS中的血管受累情况和监测治疗效果。