PurposeParkinson's disease (PD) is a well-known complex neurodegenerative disease. Typically, its identification is based on motor disorders, while the computer estimation of its main symptoms with computational machine learning (ML) has a high exposure which is supported by researches conducted. Nevertheless, ML approaches required first to refine their parameters and then to work with the best model generated. This process often requires an expert user to oversee the performance of the algorithm. Therefore, an attention is required towards new approaches for better forecasting accuracy.Design/methodology/approachTo provide an available identification model for Parkinson disease as an auxiliary function for clinicians, the authors suggest a new evolutionary classification model. The core of the prediction model is a fast learning network (FLN) optimized by a genetic algorithm (GA). To get a better subset of features and parameters, a new coding architecture is introduced to improve GA for obtaining an optimal FLN model.FindingsThe proposed model is intensively evaluated through a series of experiments based on Speech and HandPD benchmark datasets. The very popular wrappers induction models such as support vector machine (SVM), K-nearest neighbors (KNN) have been tested in the same condition. The results support that the proposed model can achieve the best performances in terms of accuracy and g-mean.Originality/valueA novel efficient PD detection model is proposed, which is called A-W-FLN. The A-W-FLN utilizes FLN as the base classifier; in order to take its higher generalization ability, and identification capability is also embedded to discover the most suitable feature model in the detection process. Moreover, the proposed method automatically optimizes the FLN's architecture to a smaller number of hidden nodes and solid connecting weights. This helps the network to train on complex PD datasets with non-linear features and yields superior result.

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