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A Multi-sequence MRI Study in Parkinson's Disease: Association Between Rigidity and Myelin
Jiayue Cai1,2, Jowon L Kim2, Tobias R Baumeister3
1School of Biomedical Engineering, Health Science Center, Shenzhen University, Shenzhen, China.
Journal of Magnetic Resonance Imaging : JMRI
|August 10, 2021
Summary
Parkinson's disease (PD) rigidity is linked to widespread myelin changes, not just functional connectivity or white matter integrity. Advanced MRI techniques reveal unique associations between myelin water fraction and rigidity.
Area of Science:
- Neuroimaging
- Neurology
- Biomedical Engineering
Background:
- The underlying mechanisms of rigidity in Parkinson's disease (PD) remain unclear.
- Advanced brain Magnetic Resonance Imaging (MRI) techniques offer potential insights into the origins of PD symptoms.
Purpose of the Study:
- To investigate the combined and distinct relationships between functional and structural MRI measures and clinical features of PD.
- To specifically explore the association of MRI markers with rigidity in Parkinson's disease.
Main Methods:
- A retrospective cross-sectional study involving 31 PD patients.
- Utilized multi-sequence MRI, including diffusion-weighted and resting-state functional MRI, on a 3T scanner.
- Assessed myelin water fraction (MWF), fractional anisotropy (FA), and functional connectivity, correlating these with motor and non-motor symptoms using multiset canonical correlation analysis (MCCA) and canonical correlation analysis (CCA).
Main Results:
- MCCA identified a joint component linking MWF, FA, and functional connectivity to age, bradykinesia, cognition, depression, and apathy, but not rigidity or tremor.
- Following adjustment for this joint component, CCA revealed a unique association between MWF and rigidity.
- No unique associations were found between FA or functional connectivity and rigidity.
Conclusions:
- Multi-sequence MRI markers like MWF, FA, and functional connectivity can characterize various PD symptoms.
- Rigidity in Parkinson's disease is uniquely associated with widespread myelin alterations, suggesting a specific pathophysiological basis.
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