Automatic classification and prediction models for early Parkinson’s disease diagnosis from SPECT imaging

•Propose methods for very accurate classification of early PD using only 4 features.•Used public database which is large and diverse making the developed models robust.•First study to develop accurate prognostic model based on SBR features for early PD. Early and accurate diagnosis of Parkinson’s di...

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Published inExpert systems with applications Vol. 41; no. 7; pp. 3333 - 3342
Main Authors Prashanth, R., Dutta Roy, Sumantra, Mandal, Pravat K., Ghosh, Shantanu
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier Ltd 01.06.2014
Elsevier
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Summary:•Propose methods for very accurate classification of early PD using only 4 features.•Used public database which is large and diverse making the developed models robust.•First study to develop accurate prognostic model based on SBR features for early PD. Early and accurate diagnosis of Parkinson’s disease (PD) is important for early management, proper prognostication and for initiating neuroprotective therapies once they become available. Recent neuroimaging techniques such as dopaminergic imaging using single photon emission computed tomography (SPECT) with 123I-Ioflupane (DaTSCAN) have shown to detect even early stages of the disease. In this paper, we use the striatal binding ratio (SBR) values that are calculated from the 123I-Ioflupane SPECT scans (as obtained from the Parkinson’s progression markers initiative (PPMI) database) for developing automatic classification and prediction/prognostic models for early PD. We used support vector machine (SVM) and logistic regression in the model building process. We observe that the SVM classifier with RBF kernel produced a high accuracy of more than 96% in classifying subjects into early PD and healthy normal; and the logistic model for estimating the risk of PD also produced high degree of fitting with statistical significance indicating its usefulness in PD risk estimation. Hence, we infer that such models have the potential to aid the clinicians in the PD diagnostic process.
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ISSN:0957-4174
1873-6793
DOI:10.1016/j.eswa.2013.11.031