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Cognitive deficits in multiple system atrophy correlate with frontal atrophy and disease duration
C C Chang1, Y Y Chang, W N Chang
1Department of Neurology, Chang Gung Memorial Hospital, Kaohsiung Medical Center, Chang Gung University College of Medicine, Kaohsiung, Taiwan. neur099@adm.cgmh.org.tw
Background And Purpose:
Dementia remains an exclusion criterion in diagnosing multiple system atrophy (MSA). This study aimed to determine the cognitive changes and brain atrophy patterns in the Parkinsonian (MSA-P) and cerebellar (MSA-C) variants of MSA.
Methods:
Voxel-based morphometry (VBM) of magnetic resonance imaging (MRI) and neuro-psychological tests were applied to 10 MSA-C and 13 MSA-P patients, and compared to 37 age-matched controls. Correlation analyses were performed between cognitive test results and morphometric data extracted from the VBM data.
Results:
In neuro-psychological testing, the 23 MSA patients scored lower in the Stroop interference test and took longer in the trail-making test as compared with the controls, whereas MSA-C performed worse than MSA-P in the memory scores, Stroop test, and time to complete the trail-making test. MSA, as a group, showed atrophy in the cerebellum, insular cortex, fusiform gyrus, inferior orbito-frontal gyrus, superior temporal gyrus, and caudate nucleus. Memory scores correlated well with pre-frontal lobe atrophy but not in the insular area.
Conclusion:
In conclusion, although dementia is not a typical presenting feature of MSA and is regarded as a sub-cortical movement disorder, frontal atrophy, cognitive changes, and dementia are identifiable as MSA progresses.
Insights
Multiple system atrophy (MSA) patients exhibit cognitive decline and brain atrophy, particularly in frontal regions, as the disease progresses. These changes, including dementia, are identifiable even though dementia is not a typical initial feature.
Area of Science:
- Neuroscience
- Neurology
- Radiology
Background:
- Multiple system atrophy (MSA) is a neurodegenerative disorder.
- Dementia is currently an exclusion criterion for MSA diagnosis.
- Understanding cognitive and atrophic changes is crucial for accurate diagnosis and management.
Purpose of the Study:
- To investigate cognitive deficits in patients with multiple system atrophy.
- To identify patterns of brain atrophy in Parkinsonian (MSA-P) and cerebellar (MSA-C) variants of MSA.
- To correlate cognitive test performance with neuroimaging findings.
Main Methods:
- Voxel-based morphometry (VBM) analysis of MRI scans.
- Neuro-psychological testing including Stroop and Trail-Making tests.
- Comparison of 10 MSA-C, 13 MSA-P patients, and 37 age-matched controls.
Main Results:
- MSA patients showed deficits in executive function (Stroop) and processing speed (Trail-Making).
- MSA-C variant patients performed worse than MSA-P on memory, Stroop, and Trail-Making tests.
- Brain atrophy was observed in the cerebellum, insula, orbito-frontal cortex, and caudate nucleus.
- Memory scores correlated with pre-frontal lobe atrophy.
Conclusions:
- Cognitive impairment and frontal atrophy are identifiable in progressive MSA.
- These findings suggest that dementia can be a feature of advanced MSA.
- Distinguishing cognitive profiles between MSA variants may aid in diagnosis.
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