Microstructural but not macrostructural cortical degeneration occurs in Parkinson’s disease with mild cognitive impairment

楔前 心理学 顶叶下小叶 帕金森病 认知障碍 神经科学 认知 心脏病学 医学 疾病 内科学
作者
Xueqin Bai,Tao Guo,Jingwen Chen,Xiaojun Guan,Cheng Zhou,Jingjing Wu,Xiaocao Liu,Haoting Wu,Jiaqi Wen,Luyan Gu,Ting Gao,Min Xuan,Peiyu Huang,Baorong Zhang,Xiaojun Xu,Minming Zhang
出处
期刊:npj Parkinson's disease 卷期号:8 (1) 被引量:2
标识
DOI:10.1038/s41531-022-00416-6
摘要

Abstract This study aimed to investigate the cortical microstructural/macrostructural degenerative patterns in Parkinson’s disease (PD) patients with mild cognitive impairment (MCI). Overall, 38 PD patients with normal cognition (PD-NC), 38 PD-MCI, and 32 healthy controls (HC) were included. PD-MCI was diagnosed according to the MDS Task Force level II criteria. Cortical microstructural alterations were evaluated with Neurite Orientation Dispersion and Density Imaging. Cortical thickness analyses were derived from T1-weighted imaging using the FreeSurfer software. For cortical microstructural analyses, compared with HC, PD-NC showed lower orientation dispersion index (ODI) in bilateral cingulate and paracingulate gyri, supplementary motor area, right paracentral lobule, and precuneus ( P FWE < 0.05); while PD-MCI showed lower ODI in widespread regions covering bilateral frontal, parietal, occipital, and right temporal areas and lower neurite density index in left frontal area, left cingulate, and paracingulate gyri ( P FWE < 0.05). Furthermore, compared with PD-NC, PD-MCI showed reduced ODI in right frontal area and bilateral caudate nuclei (voxel P < 0.01 and cluster >100 voxels) and the ODI values were associated with the Montreal Cognitive Assessment scores ( r = 0.440, P < 0.001) and the memory performance ( r = 0.333, P = 0.004) in the PD patients. However, for cortical thickness analyses, there was no difference in the between-group comparisons. In conclusion, cortical microstructural alterations may precede macrostructural changes in PD-MCI. This study provides insightful evidence for the degenerative patterns in PD-MCI and contributes to our understanding of the latent biological basis of cortical neurite changes for early cognitive impairment in PD.
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