Early diagnosis of parkinsonian disorders is feasible when the expression of disease-related metabolic brain patterns is quantified at a single-subject level.
Medical imaging techniques like fluorodeoxyglucose positron emission tomography (FDG-PET) have been used to aid in the differential diagnosis of neurodegenerative brain diseases. In this study, the objective is to classify FDG-PET brain scans of subjects with Parkinsonian syndromes
(Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy) compared to healthy controls.
The scaled subprofile model/principal component analysis (SSM/PCA) method was applied to FDG-PET brain image data to
obtain covariance patterns and corresponding subject scores. The latter were used as features for supervised classification by
the C4.5 decision tree method. Leave-one-out cross validation was applied to determine classifier performance. We carried out a
comparison with other types of classifiers. The big advantage of decision tree classification is that the results are easy to understand
by humans. A visual representation of decision trees strongly supports the interpretation process, which is very important in the context
of medical diagnosis. Further improvements are suggested based on enlarging the number of the training data, enhancing the decision
tree method by bagging, and adding additional features based on (f)MRI data.
Decision trees have been shown to be effective at classifying subjects with Parkinson's disease when provided with features (subject scores) derived from FDG-PET data. Such subject scores have strong discriminative power but are not intuitive to understand. We therefore augment each decision node with thumbnails of the principal component (PC) images from which the subject scores are computed, and also provide labeled scatter plots of the distribution of scores. These plots allow the progress of individual subjects to be traced through the tree and enable the user to focus on complex or unexpected classifications. In addition, we present a visual representation of a typical brain activity pattern arriving at each leaf node, and show how this can be compared to a known reference to validate the behaviour of the tree.
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