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February 08, 2011; 76 (6) Articles

Default mode network connectivity in stable vs progressive mild cognitive impairment

J.R. Petrella, F.C. Sheldon, S.E. Prince, V.D. Calhoun, P.M. Doraiswamy
First published January 12, 2011, DOI: https://doi.org/10.1212/WNL.0b013e31820af94e
J.R. Petrella
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F.C. Sheldon
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S.E. Prince
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V.D. Calhoun
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P.M. Doraiswamy
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Citation
Default mode network connectivity in stable vs progressive mild cognitive impairment
J.R. Petrella, F.C. Sheldon, S.E. Prince, V.D. Calhoun, P.M. Doraiswamy
Neurology Feb 2011, 76 (6) 511-517; DOI: 10.1212/WNL.0b013e31820af94e

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Abstract

Objective: Dysfunction of the default mode network (DMN) has been identified in prior cross-sectional fMRI studies of Alzheimer disease (AD) and mild cognitive impairment (MCI); however, no studies have examined its utility in predicting future cognitive decline.

Methods: fMRI scans during a face–name memory task were acquired from a cohort of 68 subjects (25 normal control, 31 MCI, and 12 AD). Subjects with MCI were followed for 2.4 years (±0.8) to determine progression to AD. Maps of DMN connectivity were compared with a template DMN map constructed from elderly normal controls to obtain goodness-of-fit (GOF) indices of DMN expression. Indices were compared between groups and correlated with cognitive decline.

Results: GOF indices were highest in normal controls, intermediate in MCI, and lowest in AD (p < 0.0001). In a predictive model (that included baseline GOF indices, age, education, Mini-Mental State Examination score, and an index of DMN gray matter volume), the effect of GOF index on progression from MCI to dementia was significant. In MCI, baseline GOF indices were correlated with change from baseline in functional status (Clinical Dementia Rating–sum of boxes) (r = −0.40, p < 0.04). However, there was no additional predictive value for DMN connectivity when baseline delayed recall was included in the models.

Conclusions: fMRI connectivity indices distinguish patients with MCI who undergo cognitive decline and conversion to AD from those who remain stable over a 2- to 3-year follow-up period. Our data support the notion of different functional brain connectivity endophenotypes for “early” vs “late” MCI, which are associated with different baseline memory scores and different rates of progression and conversion.

Footnotes

  • Study funding: Supported by NIH/NIA 1R01AG019728.

  • Editorial, page 498

  • AD
    Alzheimer disease
    CDR
    Clinical Dementia Rating
    CDR-SB
    Clinical Dementia Rating–sum of boxes
    CVLT
    California Verbal Learning Test
    DMN
    default mode network
    DSM-IV
    Diagnostic and Statistical Manual of Mental Disorders, 4th edition
    GIFT
    Group ICA of fMRI Toolbox
    GOF
    goodness-of-fit
    ICA
    independent components analyses
    MCI
    mild cognitive impairment
    MMSE
    Mini-Mental State Examination
    NINCDS-ADRDA
    National Institute of Neurological and Communicative Disorders and Stroke–Alzheimer's Disease and Related Disorders Association
    VBM
    voxel-based morphometry

  • Received August 10, 2010.
  • Accepted September 20, 2010.
  • Copyright © 2011 by AAN Enterprises, Inc.
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