CHU de Toulouse, Université de Toulouse-Toulouse 3, INSERM, UMR1214 Toulouse NeuroImaging Centre "TONIC," Center of Excellence in Neurodegeneration (CoEN), NeuroToul, Centre National de Reference AMS, Centre Expert Parkinson de Toulouse, Centre d'Investigation Clinique CIC1436, Services de Neurologie et de Pharmacologie Clinique, UMR 1048 Institute for Cardiovascular Diseases, Toulouse, France.
Division of Child and Adolescent Psychiatry, Department of Psychiatry, Stanford University School of Medicine, Stanford, California, USA.
Hum Brain Mapp. 2021 Feb 1;42(2):357-366. doi: 10.1002/hbm.25227. Epub 2020 Oct 16.
Multiple system atrophy (MSA) is a rare neurodegenerative disorder characterized by the widespread aberrant accumulation of α-synuclein (α-syn). MSA differs from other synucleinopathies such as Parkinson's disease (PD) in that α-syn accumulates primarily in oligodendrocytes, the only source of white matter myelination in the brain. Previous MSA imaging studies have uncovered focal differences in white matter. Here, we sought to build on this work by taking a global perspective on whole brain white matter. In order to do this, in vivo structural imaging and diffusion magnetic resonance imaging were acquired on 26 MSA patients, 26 healthy controls, and 23 PD patients. A refined whole brain approach encompassing the major fiber tracts and the superficial white matter located at the boundary of the cortical mantle was applied. The primary observation was that MSA but not PD patients had whole brain deep and superficial white matter diffusivity abnormalities (p < .001). In addition, in MSA patients, these abnormalities were associated with motor (Unified MSA Rating Scale, Part II) and cognitive functions (Mini-Mental State Examination). The pervasive whole brain abnormalities we observe suggest that there is widespread white matter damage in MSA patients which mirrors the widespread aggregation of α-syn in oligodendrocytes. Importantly, whole brain white matter abnormalities were associated with clinical symptoms, suggesting that white matter impairment may be more central to MSA than previously thought.
多系统萎缩症(MSA)是一种罕见的神经退行性疾病,其特征是广泛存在α-突触核蛋白(α-syn)的异常积聚。MSA 与其他突触核蛋白病(如帕金森病,PD)不同,α-syn 主要在少突胶质细胞中积聚,少突胶质细胞是大脑中白质髓鞘形成的唯一来源。先前的 MSA 成像研究已经揭示了白质中的局灶性差异。在这里,我们试图通过对整个大脑白质进行全局观察来进一步研究。为此,我们对 26 名 MSA 患者、26 名健康对照者和 23 名 PD 患者进行了活体结构成像和弥散磁共振成像。采用了一种细化的全脑方法,包括主要纤维束和位于皮质层边界的浅层白质。主要观察结果是,MSA 患者而不是 PD 患者存在整个大脑深部和浅层白质弥散异常(p < 0.001)。此外,在 MSA 患者中,这些异常与运动(统一 MSA 评定量表,第二部分)和认知功能(简易精神状态检查)相关。我们观察到的普遍的全脑异常表明 MSA 患者存在广泛的白质损伤,这与少突胶质细胞中广泛的α-syn 聚集相吻合。重要的是,全脑白质异常与临床症状相关,这表明白质损伤可能比之前认为的更为重要。