Medical Image Analysis Center, University Hospital Basel, CH-4031 Basel, Switzerland.
Hum Brain Mapp. 2010 Oct;31(10):1542-55. doi: 10.1002/hbm.20951.
The association of white matter (WM) lesions and grey matter (GM) atrophy is a feature in relapsing-remitting multiple sclerosis (RRMS). The spatiotemporal distribution pattern of WM lesions, their relations to regional GM changes and the underlying dynamics are unclear. Here we combined parametric and non-parametric voxel-based morphometry (VBM) to clarify these issues. MRI data from RRMS patients with progressive (PLV, n = 45) and non-progressive WM lesion volumes (NPLV, n = 44) followed up for 12 months were analysed. Cross-sectionally, the spatial WM lesion distribution was compared using lesion probability maps (LPMs). Longitudinally, WM lesions and GM volumes were studied using FSL-VBM and SPM5-VBM, respectively. WM lesions clustered around the lateral ventricles and in the centrum semiovale with a more widespread pattern in the PLV than in the NPLV group. The maximum local probabilities were similar in both groups and higher for T2 lesions (PLV: 27%, NPLV: 25%) than for T1 lesions (PLV: 15%, NPLV 14%). Significant WM lesion changes accompanied by cortical GM volume reductions occurred in the corpus callosum and optic radiations (P = 0.01 corrected), and more liberally tested (uncorrected P < 0.01) in the inferior fronto-occipital and longitudinal fasciculi, and corona radiata in the PLV group. Not any WM or GM changes were found in the NPLV group. In the PLV group, WM lesion distribution and development in fibres, was associated with regional GM volume loss. The different spatiotemporal distribution patterns of patients with progressive compared to patients with non-progressive WM lesions suggest differences in the dynamics of pathogenesis.
脑白质(WM)病变和灰质(GM)萎缩的相关性是复发缓解型多发性硬化症(RRMS)的特征之一。WM 病变的时空分布模式、与区域性 GM 变化的关系及其潜在的动力学机制尚不清楚。本研究结合参数和非参数基于体素的形态计量学(VBM)来阐明这些问题。分析了随访 12 个月的进展性(PLV,n = 45)和非进展性 WM 病变体积(NPLV,n = 44)RRMS 患者的 MRI 数据。在横断面上,使用病变概率图(LPM)比较空间 WM 病变分布。在纵向,分别使用 FSL-VBM 和 SPM5-VBM 研究 WM 病变和 GM 体积。WM 病变集中在侧脑室周围和半卵圆中心,PLV 组的病变分布比 NPLV 组更广泛。两组的最大局部概率相似,T2 病变(PLV:27%,NPLV:25%)的概率高于 T1 病变(PLV:15%,NPLV:14%)。在胼胝体和视辐射中观察到显著的 WM 病变变化伴随着皮质 GM 体积减少(校正后 P = 0.01),在 PLV 组中更广泛地检测到(未校正 P < 0.01)在下额枕下束和纵束,以及放射冠。在 NPLV 组中未发现任何 WM 或 GM 变化。在 PLV 组中,WM 病变的分布和纤维的发展与局部 GM 体积减少相关。与非进展性 WM 病变患者相比,进展性 WM 病变患者具有不同的时空分布模式,提示发病机制的动力学差异。