Format

Send to

Choose Destination
See comment in PubMed Commons below
JAMA Neurol. 2013 Aug;70(8):1039-45. doi: 10.1001/jamaneurol.2013.1878.

Dissociable effects of Alzheimer disease and white matter hyperintensities on brain metabolism.

Author information

1
Helen Wills Neuroscience Institute, University of California, Berkeley, Berkeley, CA 94720-3190, USA. tad@berkeley.edu

Abstract

IMPORTANCE:

Cerebrovascular disease and Alzheimer disease (AD) frequently co-occur and seem to act through different pathways in producing dementia.

OBJECTIVE:

To examine cerebrovascular disease and AD markers in relation to brain glucose metabolism in patients with mild cognitive impairment.

DESIGN AND SETTING:

Cohort study among the Alzheimer Disease Neuroimaging Initiative clinical sites in the United States and Canada.

PARTICIPANTS:

Two hundred three patients having amnestic mild cognitive impairment (74 of whom converted to AD) with serial imaging during a 3-year follow-up period.

MAIN OUTCOMES AND MEASURES:

Quantified white matter hyperintensities (WMHs) represented cerebrovascular disease, and cerebrospinal fluid β-amyloid represented AD pathology. Brain glucose metabolism in temporoparietal and frontal brain regions was measured using positron emission tomography with fluorodeoxyglucose F18.

RESULTS:

In converters, greater WMHs were associated with decreased frontal metabolism (-0.048; 95% CI, -0.067 to -0.029) but not temporoparietal metabolism (0.010; 95% CI, -0.010 to 0.030). Greater cerebrospinal fluid β-amyloid (per 10-pg/mL increase) was associated with increased temporoparietal metabolism (0.005; 95% CI, 0.000-0.010) but not frontal metabolism (0.002; 95% CI, -0.004 to 0.007) in the same patients. In nonconverters, similar relationships were observed except for a positive association of greater WMHs with increased temporoparietal metabolism (0.051; 95% CI, 0.027-0.076).

CONCLUSIONS AND RELEVANCE:

The dissociation of WMHs and cerebrospinal fluid β-amyloid in relation to regional glucose metabolism suggests that these pathologic conditions operate through different and independent pathways in AD that reflect dysfunction in different brain systems. The positive association of greater WMHs with temporoparietal metabolism suggests that these pathologic processes do not co-occur in nonconverters.

PMID:
23779022
PMCID:
PMC3779687
DOI:
10.1001/jamaneurol.2013.1878
[Indexed for MEDLINE]
PubMed Commons home

PubMed Commons

0 comments
How to join PubMed Commons

    Supplemental Content

    Full text links

    Icon for Silverchair Information Systems Icon for PubMed Central
    Loading ...
    Support Center