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Lesion Explorer: A Video-guided, Standardized Protocol for Accurate and Reliable MRI-derived Volumetrics in Alzheimer's Disease and Normal Elderly
Published on: April 14, 2014
Longitudinal volumetric MRI change and rate of cognitive decline
1Department of Neurology, School of Medicine, University of California, Davis, Sacramento, CA 95817, USA. dmmungas@ucdavis.edu
Objective:
To examine how baseline and change of volumetric MRI relate to cognitive decline in older individuals.
Background:
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.
Methods:
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.
Results:
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.
Conclusion:
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.
Insights
Memory decline in older adults is linked to hippocampal volume changes. Executive function decline is associated with multiple brain factors, including cortical gray matter and cerebrovascular disease.
Area of Science:
- Neuroimaging
- Neurology
- Gerontology
Background:
- Memory relies on hippocampal integrity; executive function is linked to frontal lobe function.
- Hippocampal and cortical atrophy correlate more strongly with cognition than cerebrovascular disease (CVD).
- Hypothesis: Memory decline relates to hippocampal volume change; executive function decline relates to cortical gray matter volume change and CVD.
Purpose of the Study:
- To investigate the relationship between baseline and changes in volumetric Magnetic Resonance Imaging (MRI) and cognitive decline in older individuals.
- To differentiate the neuroanatomical correlates of memory and executive function decline.
- To explore the roles of hippocampal volume, cortical gray matter volume, and cerebrovascular disease in cognitive aging.
Main Methods:
- Longitudinal study of 103 participants (cognitively normal, mildly impaired, demented) with cognitive evaluations and serial MRI scans.
- MRI measures included hippocampal volume (HC), cortical gray matter volume (CGM), lacune volume (LAC), and white matter hyperintensity volume (WMH).
- Random effects modeling analyzed the impact of baseline and change in MRI measures on memory (MEM) and executive function (EXEC) over time.
Main Results:
- Memory decline was associated with baseline and change in hippocampal volume (HC).
- Executive function (EXEC) decline related to baseline and change in cortical gray matter (CGM), HC, and lacune volume (LAC).
- White matter hyperintensity (WMH) was not independently associated with MEM or EXEC decline.
Conclusions:
- Hippocampal volume is a key factor in memory decline.
- Executive function decline is influenced by multiple brain components, including Alzheimer disease (AD) and cerebrovascular disease (CVD).
- Findings suggest distinct neurobiological pathways for memory and executive function decline in aging.
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