4.6 Review

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

Journal

NPJ PARKINSONS DISEASE
Volume 8, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41531-022-00416-6

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Funding

  1. 13th Five-year Plan for National Key Research and Development Program of China [2016YFC1306600]
  2. National Natural Science Foundation of China [81971577, 82171888, 82001767]
  3. Zhejiang Provincial Natural Science Foundation [LQ21H180008, LQ20H180012]
  4. Key Research and Development Program of Zhejiang Province [2020C03020]
  5. China Postdoctoral Science Foundation [2021T140599, 2019M662082]

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This study reveals cortical microstructural changes in PD-MCI patients before macrostructural changes occur. PD-NC patients typically only exhibit lower orientation dispersion index in certain brain regions, while PD-MCI patients show lower values in multiple regions for both orientation dispersion index and neurite density index.
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 Ti-weighted imaging using the FreeSurfer software. For cortical microstructural analyses, compared with HC, PD-NC showed lower orientation dispersion index (ODD 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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