Department of Anatomy and Neurosciences, Section Clinical Neuroanatomy and Biobanking, Amsterdam UMC, Location Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Amsterdam Neuroscience, Brain Imaging, Amsterdam, The Netherlands.
Mov Disord. 2023 Sep;38(9):1655-1667. doi: 10.1002/mds.29510. Epub 2023 Jun 22.
Motor and cognitive impairment in Parkinson's disease (PD) is associated with dopaminergic dysfunction that stems from substantia nigra (SN) degeneration and concomitant α-synuclein accumulation. Diffusion magnetic resonance imaging (MRI) can detect microstructural alterations of the SN and its tracts to (sub)cortical regions, but their pathological sensitivity is still poorly understood.
To unravel the pathological substrate(s) underlying microstructural alterations of SN, and its tracts to the dorsal striatum and dorsolateral prefrontal cortex (DLPFC) in PD.
Combining post-mortem in situ MRI and histopathology, T1-weighted and diffusion MRI, and neuropathological samples of nine PD, six PD with dementia (PDD), five dementia with Lewy bodies (DLB), and 10 control donors were collected. From diffusion MRI, mean diffusivity (MD) and fractional anisotropy (FA) were derived from the SN, and tracts between the SN and caudate nucleus, putamen, and DLPFC. Phosphorylated-Ser129-α-synuclein and tyrosine hydroxylase immunohistochemistry was included to quantify nigral Lewy pathology and dopaminergic degeneration, respectively.
Compared to controls, PD and PDD/DLB showed increased MD of the SN and SN-DLPFC tract, as well as increased FA of the SN-caudate nucleus tract. Both PD and PDD/DLB showed nigral Lewy pathology and dopaminergic loss compared to controls. Increased MD of the SN and FA of SN-caudate nucleus tract were associated with SN dopaminergic loss. Whereas increased MD of the SN-DLPFC tract was associated with increased SN Lewy neurite load.
In PD and PDD/DLB, diffusion MRI captures microstructural alterations of the SN and tracts to the dorsal striatum and DLPFC, which differentially associates with SN dopaminergic degeneration and Lewy neurite pathology. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
帕金森病(PD)的运动和认知障碍与多巴胺能功能障碍有关,而多巴胺能功能障碍源于黑质(SN)退化和随之而来的α-突触核蛋白积累。弥散磁共振成像(MRI)可检测 SN 及其与皮质下区域的束的微观结构改变,但它们的病理敏感性仍知之甚少。
揭示 PD 中 SN 及其向背侧纹状体和背外侧前额叶皮层(DLPFC)束的微观结构改变的病理基础。
结合死后原位 MRI 和组织病理学、T1 加权和弥散 MRI 以及 9 例 PD、6 例 PD 伴痴呆(PDD)、5 例路易体痴呆(DLB)和 10 例对照供体的神经病理学样本进行研究。从弥散 MRI 中,从 SN 及其与尾状核、壳核和 DLPFC 之间的束中得出平均扩散系数(MD)和各向异性分数(FA)。还包括磷酸化-Ser129-α-突触核蛋白和酪氨酸羟化酶免疫组织化学,以分别定量黑质Lewy 病理学和多巴胺能变性。
与对照组相比,PD 和 PDD/DLB 显示 SN 和 SN-DLPFC 束的 MD 增加,以及 SN-尾状核束的 FA 增加。PD 和 PDD/DLB 与对照组相比均显示黑质 Lewy 病理学和多巴胺能丧失。SN 和 SN-尾状核束的 MD 增加与 SN 多巴胺能丧失相关。而 SN-DLPFC 束的 MD 增加与 SN Lewy 神经丝负荷增加相关。
在 PD 和 PDD/DLB 中,弥散 MRI 可捕捉 SN 及其向背侧纹状体和 DLPFC 的束的微观结构改变,这些改变与 SN 多巴胺能变性和 Lewy 神经丝病理学的差异相关。© 2023 作者。运动障碍由 Wiley 期刊公司代表国际帕金森病和运动障碍学会出版。