4.7 Article

Neuroanatomic basis of amnestic MCI differs in patients with and without Parkinson disease

Journal

NEUROLOGY
Volume 75, Issue 22, Pages 2009-2016

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e3181ff96bf

Keywords

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Funding

  1. MEST [2010-0007749]
  2. National Research Foundation of Korea [2010-0007749] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Objective: To explore the neuroanatomic basis of amnestic mild cognitive impairment (aMCI) in patients with Parkinson disease (PD; aMCI-PD+) and without PD (aMCI-PD-). Methods: A total of 119 patients with aMCI (aMCI-PD-, n = 78, and aMCI-PD+, n = 41) underwent T1-weighted MRI, and the image data were analyzed using voxel-based morphometry. Results: No significant differences in demographic characteristics or general cognition were found between patients with aMCI-PD- and aMCI-PD+. Comparisons of neuropsychological tests between groups revealed that patients with aMCI-PD- had lower scores in delayed verbal and visual recognition memory, whereas visuospatial dysfunction was more severe in patients with aMCI-PD+. Gray matter (GM) density in the right temporal and posterior cingular cortices was significantly lower in the aMCI-PD- group compared with controls. In contrast, GM density in the aMCI-PD+ group was significantly lower in the precuneus and left prefrontal and primary motor areas relative to controls. Adirect comparison between groups showed that decreased GM density in aMCI-PD- relative to aMCI-PD+ was localized in the right temporal and anterior prefrontal areas, whereas decreased GM density in aMCI-PD+ relative to aMCI-PD- was involved in the bilateral precuneus, left primary motor, and right parietal areas. Memory decline was correlated with temporal area atrophy in aMCI-PD- and with posterior cingulate cortex atrophy in aMCI-PD+. Conclusions: Our data suggest that different neuroanatomic systems underlie memory dysfunction in patients with aMCI-PD- and aMCI-PD+. Neurology (R) 2010;75:2009-2016

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