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Pattern of Reduced Functional Connectivity and Structural Abnormalities in Parkinson's Disease: An Exploratory Study
Rachel Paes Guimarães1, Maria Cristina Arci Santos2, Alain Dagher3
1Department of Neurology, University of Campinas, Campinas, Brazil; Laboratory of Neuroimaging, University of Campinas, Campinas, Brazil; Montreal Neurological Institute, Brain Imaging Center, McGill University, Montreal, QC, Canada.
Parkinson's disease (PD) shows early structural brain changes, even in mild stages. Advanced stages reveal widespread gray matter atrophy and altered brain network connectivity, potentially serving as progression markers.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- MRI findings in Parkinson's disease (PD) are not fully understood.
- Previous studies have yielded controversial results regarding brain structural and functional alterations.
Purpose of the Study:
- To comprehensively map structural and functional brain changes in Parkinson's disease.
- To investigate how these changes correlate with disease severity.
Main Methods:
- Utilized voxel-based morphometry (VBM), cortical thickness (CT) analysis, and resting-state fMRI on 66 PD patients.
- Classified patients into mild, moderate, and severe PD groups based on the Hoehn and Yahr scale.
- Compared PD patients with controls to identify significant brain alterations.
Main Results:
- Observed gray matter atrophy in the insula and inferior frontal gyrus (moderate PD), and extended to other regions in severe PD.
- Identified progressive cortical thinning from mild to severe PD stages, affecting various brain regions.
- Detected altered functional connectivity within default mode, visual, sensorimotor, and cerebellar networks.
Conclusions:
- Cortical involvement is present even in early stages of Parkinson's disease.
- Structural and functional changes appear in similar brain regions, potentially following Braak's hypothesis.
- Combined MRI techniques offer a promising approach for monitoring disease progression and could serve as surrogate markers.
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