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Cerebral atrophy in mild cognitive impairment and Alzheimer disease: rates and acceleration
Kelvin K Leung1, Jonathan W Bartlett, Josephine Barnes
1Dementia Research Centre, UCL Institute of Neurology, Queen Square, London, UK.
Objective:
To quantify the regional and global cerebral atrophy rates and assess acceleration rates in healthy controls, subjects with mild cognitive impairment (MCI), and subjects with mild Alzheimer disease (AD).
Methods:
Using 0-, 6-, 12-, 18-, 24-, and 36-month MRI scans of controls and subjects with MCI and AD from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database, we calculated volume change of whole brain, hippocampus, and ventricles between all pairs of scans using the boundary shift integral.
Results:
We found no evidence of acceleration in whole-brain atrophy rates in any group. There was evidence that hippocampal atrophy rates in MCI subjects accelerate by 0.22%/year2 on average (p = 0.037). There was evidence of acceleration in rates of ventricular enlargement in subjects with MCI (p = 0.001) and AD (p < 0.001), with rates estimated to increase by 0.27 mL/year2 (95% confidence interval 0.12, 0.43) and 0.88 mL/year2 (95% confidence interval 0.47, 1.29), respectively. A post hoc analysis suggested that the acceleration of hippocampal loss in MCI subjects was mainly driven by the MCI subjects that were observed to progress to clinical AD within 3 years of baseline, with this group showing hippocampal atrophy rate acceleration of 0.50%/year2 (p = 0.003).
Conclusions:
The small acceleration rates suggest a long period of transition to the pathologic losses seen in clinical AD. The acceleration in hippocampal atrophy rates in MCI subjects in the ADNI seems to be driven by those MCI subjects who concurrently progressed to a clinical diagnosis of AD.
Insights
Brain atrophy accelerates in mild cognitive impairment (MCI) and Alzheimer disease (AD) patients, particularly in the hippocampus and ventricles. This acceleration suggests a prolonged transition to advanced Alzheimer disease pathology.
Area of Science:
- Neuroscience
- Medical Imaging
- Gerontology
Background:
- Alzheimer disease (AD) is characterized by progressive neurodegeneration.
- Mild cognitive impairment (MCI) represents an intermediate stage between normal aging and AD.
- Quantifying atrophy rates and their acceleration is crucial for understanding disease progression.
Purpose of the Study:
- To quantify regional and global cerebral atrophy rates.
- To assess atrophy acceleration in healthy controls, MCI, and mild AD.
- To identify patterns of neurodegeneration over time.
Main Methods:
- Utilized MRI scans from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database.
- Analyzed scans at 0, 6, 12, 18, 24, and 36 months.
- Calculated volume changes (whole brain, hippocampus, ventricles) using boundary shift integral.
Main Results:
- No acceleration in whole-brain atrophy rates observed in any group.
- Significant acceleration in hippocampal atrophy rates in MCI subjects (0.22%/year²).
- Accelerated ventricular enlargement in MCI (0.27 mL/year²) and AD (0.88 mL/year²) subjects.
Conclusions:
- Observed acceleration rates suggest a lengthy transition period to AD-related pathology.
- Hippocampal atrophy acceleration in MCI is linked to progression to clinical AD.
- Ventricular enlargement acceleration is evident in both MCI and AD stages.
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