Automated Computer Differential Classification in Parkinsonian Syndromes via Pattern Analysis on MRI1
Rationale and Objectives
Reported error rates for initial clinical diagnosis of idiopathic Parkinson's disease (IPD) against other Parkinson Plus Syndromes (PPS) can reach up to 35%. Reducing this initial error rate is an important research goal. We evaluated the ability of an automated technique, based on structural, cross-sectional T1-weighted (T1w) magnetic resonance imaging, to perform differential classification of IPD patients versus those with either progressive supranuclear palsy (PSP) or multiple systems atrophy (MSA).
Materials and Methods
A total of 181 subjects were included in this retrospective study: 149 healthy controls, 16 IPD patients, and 16 patients diagnosed with either probable PSP (n = 8) or MSA (n = 8). Cross-sectional T1w magnetic resonance imagers were acquired and subsequently corrected, scaled, resampled, and aligned within a common referential space. Tissue composition and deformation features in the hindbrain region were then automatically extracted. Classification of patients was performed using a support vector machine with least-squares optimization within a multidimensional composition/deformation feature space built from the healthy subjects' data. Leave-one-out classification was used to avoid over-determination.
Results
There were no age difference between groups. The automated system obtained 91% accuracy (agreement with long-term clinical follow-up), 88% specificity, and 93% sensitivity.
Conclusion
These results demonstrate that a classification approach based on quantitative parameters of three-dimensional hindbrain morphology extracted automatically from T1w magnetic resonance imaging has the potential to assist in the differential diagnosis of IPD versus PSP and MSA with high accuracy, therefore reducing the initial clinical error rate.
Key Words: Parkinsonian plus syndromes, brain imaging techniques, diagnosis and classification
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1 This work was supported by the Fonds de Recherche en Santé du Québec, Canada, and the Institut National pour la Santé et la Recherche en Médecine, France. The funding sources had no involvement in study design, collection, analysis, and interpretation of data, writing of the report, or in the decision to submit the paper for publication. Disclaimer: U.S. Patent pending no 10/990396.
Part of this work has been submitted as a conference abstract at the SPIE Medical Imaging conference (36).
PII: S1076-6332(08)00404-2
doi:10.1016/j.acra.2008.05.024
© 2009 AUR. Published by Elsevier Inc. All rights reserved.
