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Quantitative susceptibility mapping in atypical Parkinsonisms
Sonia Mazzucchi1, Daniela Frosini1, Mauro Costagli2
1Neurology Unit, Department of Medical Specialties, AOUP, Pisa, Italy.
Neuroimage. Clinical
|September 21, 2019
Summary
Quantitative Susceptibility Mapping (QSM) aids in differentiating Parkinson's disease (PD), Progressive Supranuclear Palsy (PSP), and Multiple System Atrophy (MSA). QSM detects iron deposition patterns in specific brain regions, improving diagnostic accuracy for these parkinsonian disorders.
Area of Science:
- Neuroimaging
- Quantitative Susceptibility Mapping (QSM)
- Degenerative Parkinsonisms
Background:
- Distinguishing Parkinson's disease (PD) from atypical parkinsonisms like Progressive Supranuclear Palsy (PSP) and Multiple System Atrophy (MSA) is clinically challenging.
- Conventional imaging lacks sensitivity for early diagnosis, necessitating advanced techniques.
- Iron-sensitive MRI, particularly Quantitative Susceptibility Mapping (QSM), offers potential for quantifying tissue iron and detecting microstructural changes.
Purpose of the Study:
- To evaluate the utility of QSM in quantifying iron content in nigral and extranigral brain regions.
- To assess the potential of QSM for differential diagnosis among PD, PSP, and MSA patients.
Main Methods:
- Sixty-five patients (36 PD, 14 MSA, 15 PSP) underwent 3T MRI with QSM.
- Regions of interest (substantia nigra, red nucleus, subthalamic nucleus, putamen, globus pallidus, caudate) were analyzed.
- Magnetic susceptibility (χ) values were compared between patient groups.
Main Results:
- QSM identified distinct iron deposition patterns: increased χ in the red nucleus, subthalamic nucleus, and medial substantia nigra for PSP.
- Significantly higher iron deposition in the putamen was observed in MSA patients.
- QSM demonstrated high diagnostic accuracy for differentiating PSP and MSA from PD.
Conclusions:
- QSM is a valuable tool for iron quantification in various brain structures affected by degenerative parkinsonisms.
- The technique shows promise for improving differential diagnosis of PD, PSP, and MSA.
- Longitudinal studies are recommended to validate QSM's ability to detect early microstructural changes.

