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PMID: 16116117 Published · ppublish English Journal Article Multicenter Study Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Longitudinal volumetric MRI change and rate of cognitive decline.

Neurology ·Vol. 65 ·No. 4 ·2005-08-23 ·Pages 565-71

Mungas D, Harvey D, Reed BR, Jagust WJ, DeCarli C, Beckett L, Mack WJ, Kramer JH, Weiner MW, Schuff N, Chui HC

Abstract

To examine how baseline and change of volumetric MRI relate to cognitive decline in older individuals. Memory is associated with hippocampal integrity, whereas executive function has been linked to impaired frontal lobe function. Previous studies have shown that hippocampal and cortical atrophy are more strongly related to cognition than are measures of subcortical cerebrovascular disease (CVD). The authors hypothesized that memory (MEM) decline would be related to change in hippocampal volume (HC), whereas decline in executive function (EXEC) would be related to change of cortical gray matter volume (CGM) and measures of subcortical CVD. Subjects from a multicenter study (n = 103) included cognitively normal, mildly impaired, and demented cases with and without subcortical lacunes. All had longitudinal cognitive evaluation (mean = 4.8 years) and two or more MRI scans at least one year apart (mean = 3.4 years). MRI measures included HC, CGM, total lacune volume (LAC), and white matter hyperintensity volume (WMH). Random effects modeling of longitudinal data assessed effects of MRI baseline and MRI change on baseline and change of psychometrically matched measures of MEM and EXEC. Change in MEM was related to HC baseline and HC change. Change in EXEC was related to baseline CGM and to change in CGM, HC, and LAC. Results were unchanged when demented cases were excluded. WMH was not associated with change in MEM or EXEC independent of HC, CGM, and LAC. Hippocampal volume was the primary determinant of memory decline, whereas executive function (EXEC) decline was related to multiple brain components. Results support a hypothesis that MEM decline is strongly influenced by Alzheimer disease (AD), whereas EXEC decline may be complexly determined by cerebrovascular disease and AD.

MeSH Terms
Aged Aged, 80 and over Aging/pathology Alzheimer Disease/diagnosis,physiopathology,psychology Atrophy/diagnosis,etiology,physiopathology Brain/pathology,physiopathology Cerebral Cortex/pathology,physiopathology Cognition Disorders/diagnosis,physiopathology,psychology Data Collection Dementia/diagnosis,physiopathology Dementia, Vascular/diagnosis,physiopathology,psychology Disease Progression Female Hippocampus/pathology,physiopathology Humans Longitudinal Studies Magnetic Resonance Imaging Male Memory Disorders/diagnosis,physiopathology,psychology Middle Aged Neuropsychological Tests Predictive Value of Tests
Authors & Affiliations
11 authors, click to expand affiliations / ORCID
Mungas D
Department of Neurology, School of Medicine, University of California, Davis, Sacramento, CA 95817, USA. dmmungas@ucdavis.edu
Harvey D
Reed B R
Jagust W J
DeCarli C
Beckett L
Mack W J
Kramer J H
Weiner M W
Schuff N
Chui H C
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Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
1526-632X
Published
2005-08-23
Pages
565-71
Language
English
Region
United States
NLM ID
0401060
PMCID
PMC1820871
Subset
IM
Grants
NIA NIH HHS · AG10129 · United States
NIA NIH HHS · R01 AG010897 · United States
NIA NIH HHS · P01 AG012435 · United States
NIA NIH HHS · AG123435 · United States
NIA NIH HHS · P30 AG010129 · United States
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