Zedde Marialuisa, Grisendi Ilaria, Assenza Federica, Napoli Manuela, Moratti Claudio, Di Cecco Giovanna, D'Aniello Serena, Valzania Franco, Pascarella Rosario
Neurology Unit, Stroke Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123 Reggio Emilia, Italy.
Neuroradiology Unit, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Viale Risorgimento 80, 42123 Reggio Emilia, Italy.
J Clin Med. 2024 Mar 28;13(7):1969. doi: 10.3390/jcm13071969.
Secondary neurodegeneration refers to the final result of several simultaneous and sequential mechanisms leading to the loss of substance and function in brain regions connected to the site of a primary injury. Stroke is one of the most frequent primary injuries. Among the subtypes of post-stroke secondary neurodegeneration, axonal degeneration of the corticospinal tract, also known as Wallerian degeneration, is the most known, and it directly impacts motor functions, which is crucial for the motor outcome. The timing of its appearance in imaging studies is usually considered late (over 4 weeks), but some diffusion-based magnetic resonance imaging (MRI) techniques, as diffusion tensor imaging (DTI), might show alterations as early as within 7 days from the stroke. The different sequential pathological stages of secondary neurodegeneration provide an interpretation of the signal changes seen by MRI in accordance with the underlying mechanisms of axonal necrosis and repair. Depending on the employed MRI technique and on the timing of imaging, different rates and thresholds of Wallerian degeneration have been provided in the literature. In fact, three main pathological stages of Wallerian degeneration are recognizable-acute, subacute and chronic-and MRI might show different changes: respectively, hyperintensity on T2-weighted sequences with corresponding diffusion restriction (14-20 days after the injury), followed by transient hypointensity of the tract on T2-weighted sequences, and by hyperintensity and atrophy of the tract on T2-weighted sequences. This is the main reason why this review is focused on MRI signal changes underlying Wallerian degeneration. The identification of secondary neurodegeneration, and in particular Wallerian degeneration, has been proposed as a prognostic indicator for motor outcome after stroke. In this review, the main mechanisms and neuroimaging features of Wallerian degeneration in adults are addressed, focusing on the time and mechanisms of tissue damage underlying the signal changes in MRI.
继发性神经退行性变是指几种同时发生和相继出现的机制所导致的最终结果,这些机制会致使与原发性损伤部位相连的脑区出现物质丧失和功能减退。中风是最常见的原发性损伤之一。在中风后继发性神经退行性变的亚型中,皮质脊髓束的轴索性变性,也称为华勒氏变性,最为人所知,它直接影响运动功能,而运动功能对运动结局至关重要。其在影像学研究中出现的时间通常被认为较晚(超过4周),但一些基于扩散的磁共振成像(MRI)技术,如扩散张量成像(DTI),可能早在中风后7天内就会显示出改变。继发性神经退行性变不同的相继病理阶段,根据轴突坏死和修复的潜在机制,对MRI所见的信号变化作出了解释。根据所采用的MRI技术和成像时间,文献中给出了华勒氏变性的不同速率和阈值。事实上,华勒氏变性可识别出三个主要病理阶段——急性期、亚急性期和慢性期——MRI可能会显示出不同的变化:分别为T2加权序列上的高信号并伴有相应的扩散受限(损伤后14 - 20天),随后是该束在T2加权序列上短暂的低信号,以及T2加权序列上该束的高信号和萎缩。这就是本综述聚焦于华勒氏变性潜在的MRI信号变化的主要原因。继发性神经退行性变,尤其是华勒氏变性的识别,已被提议作为中风后运动结局的预后指标。在本综述中,将探讨成人群体中华勒氏变性的主要机制和神经影像学特征,重点关注MRI信号变化背后组织损伤的时间和机制。