Department of Neurology with Institute of Translational Neurology, University Hospital Münster, Albert-Schweitzer-Campus 1, Building A1, 48149, Münster, Germany.
Department of Neuropathology, University Medical Center Göttingen, Robert-Koch-Str. 40, 37075, Göttigen, Germany.
Prog Neurobiol. 2019 Nov;182:101663. doi: 10.1016/j.pneurobio.2019.101663. Epub 2019 Jul 30.
Magnetic resonance imaging (MRI) is the most important tool for diagnosing multiple sclerosis (MS). However, MRI is still unable to precisely quantify the specific pathophysiological processes that underlie imaging findings in MS. Because autopsy and biopsy samples of MS patients are rare and biased towards a chronic burnt-out end or fulminant acute early stage, the only available methods to identify human disease pathology are to apply MRI techniques in combination with subsequent histopathological examination to small animal models of MS and to transfer these insights to MS patients. This review summarizes the existing combined imaging and histopathological studies performed in MS mouse models and humans with MS (in vivo and ex vivo), to promote a better understanding of the pathophysiology that underlies conventional MRI, diffusion tensor and magnetization transfer imaging findings in MS patients. Moreover, it provides a critical view on imaging capabilities and results in MS patients and mouse models and for future studies recommends how to combine those particular MR sequences and parameters whose underlying pathophysiological basis could be partly clarified. Further combined longitudinal in vivo imaging and histopathological studies on rationally selected, appropriate mouse models are required.
磁共振成像(MRI)是诊断多发性硬化症(MS)的最重要工具。然而,MRI 仍然无法准确地量化 MS 影像学表现背后的特定病理生理过程。由于 MS 患者的尸检和活检样本很少,而且偏向于慢性耗竭终末期或暴发性急性早期,因此唯一可用于识别人类疾病病理学的方法是将 MRI 技术应用于 MS 的小动物模型,并将这些见解转移到 MS 患者身上。这篇综述总结了在 MS 小鼠模型和 MS 患者(体内和体外)中进行的现有的联合成像和组织病理学研究,以促进更好地理解 MS 患者常规 MRI、弥散张量和磁化传递成像结果背后的病理生理学。此外,它对 MS 患者和小鼠模型的成像能力和结果提出了批判性的看法,并为未来的研究建议了如何结合那些特定的 MR 序列和参数,这些序列和参数的潜在病理生理学基础部分已经得到阐明。需要在合理选择的适当小鼠模型上进行进一步的联合纵向体内成像和组织病理学研究。