4.7 Article

Joint detection and clinical score prediction in Parkinson's disease via multi-modal sparse learning

Journal

EXPERT SYSTEMS WITH APPLICATIONS
Volume 80, Issue -, Pages 284-296

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.eswa.2017.03.038

Keywords

Parkinson's disease; Feature selection; Classification; Prediction; Multi-modal data

Funding

  1. China 863 program [2015AA015305]
  2. National Natural Science Foundation of China [U1301252, 61402296, 61471243]
  3. Guangdong Key Laboratory Project [2012A061400024]
  4. Guangdong Medical Grant [B2016094]
  5. Natural Science Foundation of Shenzhen [JCYJ20140418095735561, JCYJ20150731160834611]
  6. Shenzhen Key Basic Research Project [JCYJ20150525092940986]
  7. Open Fund Project of Fujian Provincial Key Laboratory of Information Processing and Intelligent Control (Minjiang University) [MJUKF201711]
  8. National Natural Science Foundation of Shenzhen University [2016077]

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Parkinson's disease (PD) is the world's second most common progressive neurodegenerative disease. This disease is characterized by a combination of various non-motor symptoms (e.g., depression, olfactory, and sleep disturbance) and motor symptoms (e.g., bradykinesia, tremor, rigidity), therefore diagnosis and treatment of PD are usually complex. There are some machine learning techniques that automate PD diagnosis and predict clinical scores. These techniques are promising in assisting assessment of stage of pathology and predicting PD progression. However, existing PD research mainly focuses on single-function model (i.e., only classification or prediction) using one modality, which limits performance. In this work, we propose a novel feature selection framework based on multi-modal neuroimaging data for joint PD detection and clinical score prediction. Specifically, a unique objective function is designed to capture discriminative features which are used to train a support vector regression (SVR) model for predicting clinical score (e.g., sleep scores and olfactory scores), and a support vector classification (SVC) model for class label identification. We evaluate our method using a dataset of 208 subjects, which includes 56 normal controls (NC), 123 PD and 29 scans without evidence of dopamine deficit (SWEDD) via a 10 fold cross-validation strategy. Our experimental results demonstrate that multi-modal data effectively improves the performance in disease status identification and clinical scores prediction as compared to one single modality. Comparative analysis reveals that the proposed method outperforms state-of-art methods. (C) 2017 Elsevier Ltd. All rights reserved.

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