Su Dongning, Gan Yawen, Zhang Zhe, Cui Yusha, Zhang Zhijin, Liu Zhu, Wang Zhan, Zhou Junhong, Sossi Vesna, Stoessl A Jon, Wu Tao, Jing Jing, Feng Tao
Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
China National Clinical Research Center for Neurological Diseases, Beijing, China.
Mov Disord. 2023 Apr;38(4):616-625. doi: 10.1002/mds.29320. Epub 2023 Feb 17.
Degeneration of the substantia nigra (SN) may contribute to levodopa-induced dyskinesia (LID) in Parkinson's disease (PD), but the exact characteristics of SN in LID remain unclear.
To further understand the pathogenesis of patients with PD with LID (PD-LID), we explored the structural and functional characteristics of SN in PD-LID using multimodal magnetic resonance imaging (MRI).
Twenty-nine patients with PD-LID, 37 patients with PD without LID (PD-nLID), and 28 healthy control subjects underwent T1-weighted MRI, quantitative susceptibility mapping, neuromelanin-sensitive MRI, multishell diffusion MRI, and resting-state functional MRI. Different measures characterizing the SN were obtained using a region of interest-based approach.
Compared with patients with PD-nLID and healthy control subjects, the quantitative susceptibility mapping values of SN pars compacta (SNpc) were significantly higher (P = 0.049 and P = 0.00002), and the neuromelanin contrast-to-noise ratio values in SNpc were significantly lower (P = 0.012 and P = 0.000002) in PD-LID. The intracellular volume fraction of the posterior SN in PD-LID was significantly higher compared with PD-nLID (P = 0.037). Resting-state fMRI indicated that PD-LID in the medication off state showed higher functional connectivity between the SNpc and putamen compared with PD-nLID (P = 0.031), and the functional connectivity changes in PD-LID were positively correlated with Unified Dyskinesia Rating Scale total scores (R = 0.427, P = 0.042).
Our multimodal imaging findings highlight greater neurodegeneration in SN and the altered nigrostriatal connectivity in PD-LID. These characteristics provide a new perspective into the role of SN in the pathophysiological mechanisms underlying PD-LID. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
黑质(SN)变性可能与帕金森病(PD)中的左旋多巴诱导的异动症(LID)有关,但LID中SN的确切特征仍不清楚。
为了进一步了解帕金森病伴LID(PD-LID)患者的发病机制,我们使用多模态磁共振成像(MRI)探索了PD-LID中SN的结构和功能特征。
29例PD-LID患者、37例无LID的PD患者(PD-nLID)和28名健康对照者接受了T1加权MRI、定量磁化率成像、神经黑色素敏感MRI、多壳层扩散MRI和静息态功能MRI检查。使用基于感兴趣区域的方法获得表征SN的不同测量值。
与PD-nLID患者和健康对照者相比,PD-LID中致密部黑质(SNpc)的定量磁化率成像值显著更高(P = 0.049和P = 0.00002),且SNpc中的神经黑色素对比噪声比值显著更低(P = 0.012和P = 0.000002)。与PD-nLID相比,PD-LID中SN后部的细胞内体积分数显著更高(P = 0.037)。静息态功能磁共振成像表明,与PD-nLID相比,处于停药状态的PD-LID在SNpc和壳核之间表现出更高的功能连接性(P = 0.031),且PD-LID中的功能连接性变化与统一异动症评定量表总分呈正相关(R = 0.427,P = 0.042)。
我们的多模态成像结果突出了PD-LID中SN更大程度的神经变性以及黑质纹状体连接性的改变。这些特征为SN在PD-LID潜在病理生理机制中的作用提供了新的视角。© 2023作者。《运动障碍》由Wiley Periodicals LLC代表国际帕金森和运动障碍协会出版。