John L. Trotter Multiple Sclerosis Center and Neuroimmunology Section, Department of Neurology, School of Medicine, Washington University in St. Louis, St Louis, MO, USA.
Department of Radiology, Mallinckrodt Institute of Radiology, School of Medicine, Washington University in St. Louis, St Louis, MO, USA.
Mult Scler. 2019 Dec;25(14):1937-1941. doi: 10.1177/1352458518786072. Epub 2018 Jul 11.
Diffusion basis spectrum imaging (DBSI) models diffusion-weighted magnetic resonance imaging (MRI) signals as a combination of discrete anisotropic diffusion tensors and a spectrum of isotropic diffusion tensors. Here, we report the histopathological correlates of DBSI in the biopsied brain tissue of a patient with an inflammatory demyelinating lesion typical of multiple sclerosis (MS). Increased radial diffusivity (marker of demyelination), decreased fiber fraction (apparent axonal density), elevated nonrestricted isotropic fraction (marker of vasogenic edema), but unchanged axial diffusivity (marker of integrity of residual axons) seen in the lesion appeared consistent with histopathological findings of inflammatory demyelination with relative axonal sparing. Our report supports the application of DBSI as a biomarker in human studies of MS.
扩散基础谱成像(DBSI)模型将扩散加权磁共振成像(MRI)信号表示为离散各向异性扩散张量和各向同性扩散张量谱的组合。在这里,我们报告了一位炎症性脱髓鞘病变患者(多发性硬化症(MS)的典型病变)的活检脑组织中 DBSI 的组织病理学相关性。病变中观察到的径向扩散率增加(脱髓鞘标志物)、纤维分数降低(明显轴突密度)、不受限制的各向同性分数升高(血管源性水肿标志物),而轴突扩散率不变(残余轴突完整性标志物),与炎症性脱髓鞘伴相对轴突保留的组织病理学发现一致。我们的报告支持将 DBSI 作为 MS 人类研究中的生物标志物的应用。