Imbalanced optimal feedback motor control system in spinocerebellar ataxia type 3

Author:

Li Leinian12,Chen Hui1,Deng LiHua1,Huang YongHua1,Zhang YuHan1,Luo YueYuan1,Ou PeiLing1,Shi LinFeng1,Dai LiMeng3,Chen Wei4,Chen HuaFu15,Wang Jian1,Liu Chen1ORCID

Affiliation:

1. 7T Magnetic Resonance Translational Medicine Research Center, Department of Radiology, Southwest Hospital Army Medical University (Third Military Medical University) Chongqing China

2. School of Psychology Shandong Normal University Jinan China

3. Department of Medical Genetics, College of Basic Medical Science Army Medical University (Third Military Medical University) Chongqing China

4. MR Research Collaboration Team Siemens Healthineers Ltd. Wuhan China

5. MOE Key Laboratory for Neuro Information, High‐Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province University of Electronic Science and Technology of China Chengdu China

Abstract

AbstractBackground and purposeHuman motor planning and control depend highly on optimal feedback control systems, such as the neocortex–cerebellum circuit. Here, diffusion tensor imaging was used to verify the disruption of the neocortex–cerebellum circuit in spinocerebellar ataxia type 3 (SCA3), and the circuit's disruption correlation with SCA3 motor dysfunction was investigated.MethodsThis study included 45 patients with familial SCA3, aged 17–67 years, and 49 age‐ and sex‐matched healthy controls, aged 21–64 years. Tract‐based spatial statistics and probabilistic tractography was conducted using magnetic resonance images of the patients and controls. The correlation between the local probability of probabilistic tractography traced from the cerebellum and clinical symptoms measured using specified symptom scales was also calculated.ResultsThe cerebellum‐originated probabilistic tractography analysis showed that structural connectivity, mainly in the subcortical cerebellar–thalamo–cortical tract, was significantly reduced and the cortico–ponto–cerebellar tract was significantly stronger in the SCA3 group than in the control group. The enhanced tract was extended to the right lateral parietal region and the right primary motor cortex. The enhanced neocortex–cerebellum connections were highly associated with disease progression, including duration and symptomatic deterioration. Tractography probabilities from the cerebellar to parietal and sensorimotor areas were significantly negatively correlated with motor abilities in patients with SCA3.ConclusionTo our knowledge, this study is the first to reveal that disrupting the neocortex–cerebellum loop can cause SCA3‐induced motor dysfunctions. The specific interaction between the cerebellar–thalamo–cortical and cortico–ponto–cerebellar pathways in patients with SCA3 and its relationship with ataxia symptoms provides a new direction for future research.

Funder

National Natural Science Foundation of China

Publisher

Wiley

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