Gracien René-Maxime, Reitz Sarah C, Hof Stephanie-Michelle, Fleischer Vinzenz, Zimmermann Hilga, Droby Amgad, Steinmetz Helmuth, Zipp Frauke, Deichmann Ralf, Klein Johannes C
Department of Neurology, Goethe University, Frankfurt/Main, Germany.
Brain Imaging Center, Goethe University, Frankfurt/Main, Germany.
NMR Biomed. 2016 Apr;29(4):444-50. doi: 10.1002/nbm.3486. Epub 2016 Jan 28.
T2 relaxation time is a quantitative MRI in vivo surrogate of cerebral tissue damage in multiple sclerosis (MS) patients. Cortical T2 prolongation is a known feature in later disease stages, but has not been demonstrated in the cortical normal appearing gray matter (NAGM) in early MS. This study centers on the quantitative evaluation of the tissue parameter T2 in cortical NAGM in a collective of early MS and clinically isolated syndrome (CIS) patients, hypothesizing that T2 prolongation is already present at early disease stages and variable over space, in line with global and focal inflammatory processes in MS. Additionally, magnetization transfer ratio (MTR) mapping was performed for further characterization of the expected cortical T2 alteration. Quantitative T2 and MTR maps were acquired from 12 patients with CIS and early MS, and 12 matched healthy controls. The lesion-free part of the cortical volume was identified, and the mean T2 and MTR values and their standard deviations within the cortical volume were determined. For evaluation of spatial specificity, cortical lobar subregions were tested separately for differences of mean T2 and T2 standard deviation. We detected significantly prolonged T2 in cortical NAGM in patients. T2 prolongation was found across the whole cerebral cortex and in all individual lobar subregions. Significantly higher standard deviations across the respective region of interest were found for the whole cerebral cortex and all subregions, suggesting the occurrence of spatially inhomogeneous cortical damage in all regions studied. A trend was observed for MTR reduction and increased MTR variability across the whole cortex in the MS group, suggesting demyelination. In conclusion, our results suggest that cortical damage in early MS is evidenced by spatially inhomogeneous T2 prolongation which goes beyond demyelination. Iron deposition, which is known to decrease T2, seems less prominent.
T2弛豫时间是多发性硬化症(MS)患者脑组织损伤的一种定量磁共振成像(MRI)体内替代指标。皮质T2延长是疾病后期已知的特征,但在早期MS的皮质正常外观灰质(NAGM)中尚未得到证实。本研究聚焦于对一组早期MS和临床孤立综合征(CIS)患者皮质NAGM中组织参数T2的定量评估,假设T2延长在疾病早期就已存在且在空间上存在差异,这与MS中的整体和局灶性炎症过程一致。此外,进行了磁化传递率(MTR)映射以进一步表征预期的皮质T2改变。从12例CIS和早期MS患者以及12名匹配的健康对照者中获取了定量T2和MTR图谱。确定了皮质体积中无病变的部分,并测定了皮质体积内的平均T2和MTR值及其标准差。为了评估空间特异性,分别对皮质叶亚区域的平均T2和T2标准差差异进行了测试。我们在患者的皮质NAGM中检测到T2明显延长。在整个大脑皮质和所有单个叶亚区域均发现T2延长。在整个大脑皮质和所有亚区域的相应感兴趣区域中发现标准差显著更高,表明在所有研究区域均发生了空间不均匀的皮质损伤。在MS组中观察到整个皮质的MTR降低和MTR变异性增加的趋势,提示存在脱髓鞘。总之,我们的结果表明,早期MS中的皮质损伤表现为空间不均匀的T2延长,这超出了脱髓鞘的范围。已知会降低T2的铁沉积似乎不太明显。