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Author Spotlight: Establishing a New Fluorescence-Based Protocol for In Vivo Mitochondrial Morphology Analysis in Parkinson's Disease
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No relevant midbrain atrophy in Parkinson's disease
E Mäkinen1, J Joutsa2,3, J Isotalo2
1Division of Clinical Neurosciences, Turku University Hospital and University of Turku, Turku, Finland. elmama@utu.fi.
Acta Neurologica Scandinavica
|June 7, 2016
Summary
Mild midbrain atrophy is present in Parkinson's disease (PD) but does not predict striatal dopaminergic degeneration. MRI-detected midbrain atrophy in PD is not a clinically useful marker for dopamine function.
Area of Science:
- Neuroimaging
- Neurology
- Radiology
Background:
- Parkinson's disease (PD) is characterized by the degeneration of dopaminergic neurons.
- Midbrain structural changes may occur in PD, but their relationship with dopaminergic deficits is unclear.
Purpose of the Study:
- To determine if midbrain atrophy is present in Parkinson's disease (PD).
- To assess if midbrain atrophy can serve as a marker for striatal dopaminergic degeneration in PD.
Main Methods:
- 150 PD patients and 155 controls underwent dopamine transporter (DAT) SPECT ([123I]FP-CIT) and 1.5T MRI.
- Midbrain atrophy was quantified using midbrain-to-pons ratios from MRI.
- DAT binding was analyzed using region-of-interest and voxel-based methods.
Main Results:
- PD patients exhibited slightly lower midbrain-to-pons ratios compared to controls (P < 0.05).
- No significant correlation was found between midbrain atrophy and striatal or extrastriatal DAT binding in PD patients or controls.
Conclusions:
- Mild midbrain atrophy is detectable in Parkinson's disease (PD) via MRI.
- Midbrain atrophy in PD is not associated with the degree of striatal dopaminergic dysfunction.
- Midbrain atrophy measurements are not clinically useful predictors of dopamine function in PD.
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