Whole-brain atrophy rate and cognitive decline: longitudinal MR study of memory clinic patients
Jasper D Sluimer1, Wiesje M van der Flier, Giorgos B Karas
1Department of Diagnostic Radiology, Alzheimer Centre, Vrije Universiteit Medical Centre, Amsterdam, the Netherlands. jd.sluimer@vumc.nl
Purpose:
To prospectively determine whole-brain atrophy rate in mild cognitive impairment (MCI) and Alzheimer disease (AD) and its association with cognitive decline, and investigate the risk of progression to dementia in initially nondemented patients given baseline brain volume and whole-brain atrophy rate.
Materials And Methods:
This study was IRB approved; written informed consent was obtained; and included 65 AD patients (38 women, 27 men; age, 52-81 years), 45 MCI patients (22 women, 23 men; age, 56-80 years), 27 patients with subjective complaints (12 women, 15 men; age, 50-87 years), and 10 healthy controls (six women, four men; age, 53-80 years). Two magnetic resonance (MR) images were acquired at average interval of 1.8 years +/- 0.7 (standard deviation). Baseline brain volume and whole-brain atrophy rates were measured on three-dimensional T1-weighted MR images (1.0 T; single slab, 168 sections; matrix size, 256 x 256; field of view, 250 mm; voxel size, 1 x 1 x 1.5 mm; repetition time msec/echo time msec/inversion time msec, 15/7/300; and flip angle, 15 degrees ). Associations were assessed by using partial-correlations. Cox proportional hazards models were used to estimate risk of developing dementia.
Results:
Baseline brain volume was lowest in AD but did not differ significantly between MCI, subjective complaints, and control groups (P > .38). Whole-brain atrophy rates were higher in AD (-1.9% per year +/- 0.9) than MCI (-1.2% per year +/- 0.9, P = .003) patients, who had higher whole-brain atrophy rates than patients with subjective complaints (-0.7% per year +/- 0.7, P = .03) and controls (-0.5% per year +/- 0.5, P = .05). Whole-brain atrophy rate correlated with annualized Mini-Mental State Examination (MMSE) change (r = 0.48, P < .001), while baseline volume did not (r = 0.11, P = .22). Cox models showed that-after correction for age, sex, and baseline MMSE-a higher whole-brain atrophy rate was associated with an increased risk of progression to dementia (highest vs lowest tertile [hazard ratio, 3.6; 95% confidence interval: 1.2, 11.4]).
Conclusion:
Whole-brain atrophy rate was strongly associated with cognitive decline. In nondemented participants, a high whole-brain atrophy rate was associated with an increased risk of progression to dementia.
Insights
Whole-brain atrophy rate, a measure of brain shrinkage, is strongly linked to cognitive decline in Alzheimer's disease and mild cognitive impairment. Higher atrophy rates predict an increased risk of developing dementia.
Area of Science:
- Neurology
- Neuroimaging
- Geriatrics
Background:
- Mild cognitive impairment (MCI) and Alzheimer's disease (AD) are associated with brain volume changes.
- Quantifying whole-brain atrophy rates can help understand disease progression and predict dementia risk.
Purpose of the Study:
- To prospectively determine whole-brain atrophy rates in MCI and AD patients.
- To assess the association between atrophy rates and cognitive decline.
- To investigate the risk of dementia progression in non-demented individuals based on baseline brain volume and atrophy rate.
Main Methods:
- Prospective study including 65 AD patients, 45 MCI patients, 27 with subjective complaints, and 10 controls.
- Two MRI scans were acquired approximately 1.8 years apart to measure baseline brain volume and whole-brain atrophy rates.
- Partial correlations and Cox proportional hazards models were used to analyze associations with cognitive decline and dementia risk.
Main Results:
- Whole-brain atrophy rates were significantly higher in AD patients (-1.9%/year) compared to MCI patients (-1.2%/year), subjective complaints (-0.7%/year), and controls (-0.5%/year).
- Higher whole-brain atrophy rates correlated with greater annualized cognitive decline (r = 0.48, P < .001).
- A higher whole-brain atrophy rate was associated with an increased risk of progression to dementia (HR, 3.6; 95% CI: 1.2, 11.4) after adjusting for baseline factors.
Conclusions:
- Whole-brain atrophy rate is a significant indicator of cognitive decline in neurodegenerative diseases.
- In non-demented individuals, a rapid rate of whole-brain atrophy is a predictor of future dementia development.
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