From the Departments of Radiology (S.Z., T.D.N., S.P., I.K., P.S., Y.W., S.A.G.).
Department of Radiology (S.Z.), Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
AJNR Am J Neuroradiol. 2019 Jun;40(6):987-993. doi: 10.3174/ajnr.A6071. Epub 2019 May 16.
MR imaging studies have demonstrated that magnetic susceptibility in multiple sclerosis lesions is dependent on lesion age. The objective of this study was to use quantitative susceptibility mapping to determine whether lesions with a hyperintense rim, indicative of iron-laden inflammatory cells (rim+), follow a unique time-dependent trajectory of susceptibility change compared with those without (rim-).
We studied patients with MS with at least 1 new gadolinium-enhancing lesion and at least 3 longitudinal quantitative susceptibility mapping scans obtained between 1.1 and 6.1 years. Lesions were classified as rim+ if a hyperintense rim appeared on quantitative susceptibility mapping at any time. A multilevel growth curve model compared longitudinal susceptibility among rim+ and rim- lesions.
Thirty-two new gadolinium-enhancing lesions from 19 patients with MS were included, and 16 lesions (50%) were identified as rim+. Quantitative susceptibility mapping rim+ lesions were larger than rim- lesions with gadolinium enhancement ( < .001). Among all lesions, susceptibility increased sharply after enhancement to a peak between 1 and 2 years followed by a decrease. The overall susceptibility curve height for rim- lesions was 4.27 parts per billion lower than that for rim+ lesions ( = .01). Rim- lesions demonstrated a higher linear slope relative to rim+ lesions ( = .023) but faster cubic decay relative to rim+ lesions ( = .005). Rim- lesions started decaying approximately 2 years earlier compared with rim+ lesions.
There was a marked difference in the susceptibility temporal trajectory between rim+ and rim- lesions during the first 6 years of lesion formation. Most rim+ lesions retain iron for years after the initial lesion appearance.
磁共振成像研究表明,多发性硬化症病变的磁化率取决于病变的年龄。本研究的目的是使用定量磁化率映射来确定具有提示含铁炎症细胞的高信号边缘( rim+)的病变是否与没有这种边缘的病变( rim-)相比,具有独特的随时间变化的磁化率变化轨迹。
我们研究了至少有 1 个新的钆增强病变且至少有 3 个在 1.1 到 6.1 年内获得的纵向定量磁化率映射扫描的多发性硬化症患者。如果在任何时间定量磁化率映射上出现高信号边缘,则将病变归类为 rim+。采用多级生长曲线模型比较 rim+和 rim-病变的纵向磁化率。
共纳入了 19 例多发性硬化症患者的 32 个新的钆增强病变,其中 16 个病变(50%)被确定为 rim+。定量磁化率映射 rim+病变的大小大于伴有钆增强的 rim-病变(<0.001)。在所有病变中,磁化率在增强后急剧增加,达到 1 到 2 年之间的峰值,然后下降。与 rim+病变相比,rim-病变的总体磁化率曲线高度低 4.27 十亿分之一( =.01)。rim-病变相对于 rim+病变具有更高的线性斜率( =.023),但相对于 rim+病变具有更快的立方衰减( =.005)。与 rim+病变相比,rim-病变的衰减开始早约 2 年。
在病变形成的前 6 年中,rim+和 rim-病变之间的磁化率时间轨迹存在明显差异。大多数 rim+病变在初始病变出现后多年仍保留铁。