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November 30, 2010; 75 (22) Articles

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

J.E. Lee, H.-J. Park, S.K. Song, Y.H. Sohn, J.D. Lee, P.H. Lee
First published November 29, 2010, DOI: https://doi.org/10.1212/WNL.0b013e3181ff96bf
J.E. Lee
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H.-J. Park
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S.K. Song
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Y.H. Sohn
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J.D. Lee
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Citation
Neuroanatomic basis of amnestic MCI differs in patients with and without Parkinson disease
J.E. Lee, H.-J. Park, S.K. Song, Y.H. Sohn, J.D. Lee, P.H. Lee
Neurology Nov 2010, 75 (22) 2009-2016; DOI: 10.1212/WNL.0b013e3181ff96bf

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Abstract

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. A direct 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+.

Footnotes

  • Study funding: Supported by Mid-career Researcher Program through NRF grant funded by the MEST (2010-0007749).

  • AD
    Alzheimer disease
    ADL
    activities of daily living
    aMCI
    amnestic mild cognitive impairment
    aMCI-PD+
    patients with amnestic mild cognitive impairment with Parkinson disease
    aMCI-PD−
    patients with amnestic mild cognitive impairment without Parkinson disease
    CDR
    Clinical Dementia Rating
    COWAT
    Controlled Oral Word Association Test
    GM
    gray matter
    K-BNT
    Korean version of the Boston Naming Test
    MCI
    mild cognitive impairment
    PD
    Parkinson disease
    RCFT
    Rey Complex Figure Test
    SNSB
    Seoul Neuropsychological Screening Battery
    SVLT
    Seoul Verbal Learning Test
    UPDRS-III
    Unified Parkinson's Disease Rating Scale Part III
    VBM
    voxel-based morphometry

  • Supplemental data at www.neurology.org

  • Received May 13, 2010.
  • Accepted August 12, 2010.
  • Copyright © 2010 by AAN Enterprises, Inc.
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