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Published on: January 5, 2016
Basal Forebrain Volume Predicts Disease Conversion in Prodromal Synucleinopathy.
Lachlan Churchill1,2,3, Ajay Konuri1,2, Anna Ignatavicius1,2
1Faculty of Medicine and Health, Central Clinical School, University of Sydney, Sydney, New South Wales, Australia.
Bilateral basal forebrain (BF) atrophy in isolated rapid eye movement sleep behavior disorder (iRBD) predicts conversion to Parkinson's disease (PD) or dementia with Lewy bodies (DLB). Left BF atrophy specifically indicates higher DLB risk, highlighting BF degeneration as a key biomarker.
Area of Science:
- Neuroscience
- Neurology
- Radiology
Background:
- Isolated rapid eye movement sleep behavior disorder (iRBD) is a prodromal stage for Parkinson's disease (PD) and dementia with Lewy bodies (DLB).
- The basal forebrain (BF) is implicated in Lewy body disorders, but its role in early iRBD phenoconversion is unclear.
- Previous studies linked bilateral BF atrophy to cognitive decline in iRBD.
Purpose of the Study:
- To investigate basal forebrain (BF) gray matter volume differences in iRBD patients versus controls.
- To assess the predictive utility of BF volume for phenoconversion to PD or DLB.
- To explore lateralized BF atrophy effects on disease conversion.
Main Methods:
- 41 iRBD patients and 38 controls underwent MRI and longitudinal clinical assessment.
- Baseline T1-weighted MRI was used to measure left and right BF gray matter volumes.
- Cox proportional hazards models analyzed BF volumes as predictors of phenoconversion risk.
Main Results:
- No significant group differences in BF volume were observed.
- Lower BF volume correlated with poorer global cognition in iRBD.
- Bilateral BF atrophy predicted increased risk of conversion to PD or DLB.
- Left BF atrophy specifically predicted conversion to DLB.
Conclusions:
- Bilateral basal forebrain (BF) atrophy may serve as an early biomarker for phenoconversion in iRBD.
- Left-sided BF atrophy may indicate a heightened risk for developing dementia with Lewy bodies (DLB).
- BF degeneration holds prognostic value in prodromal synucleinopathies.
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