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Parkinson's disease (PD) is the second most common progressive neurological condition after Alzheimer's. The significant number of individuals afflicted with this illness makes it essential to develop a method to diagnose the conditions in their early phases. PD is typically identified from motor symptoms or via other Neuroimaging techniques. Expensive, time-consuming, and unavailable to the general public, these methods are not very accurate. Another issue to be addressed is the black-box nature of machine learning methods that needs interpretation. These issues encourage us to develop a novel technique using Shapley additive explanations (SHAP) and Hard Voting Ensemble Method based on voice signals to diagnose PD more accurately. Another purpose of this study is to interpret the output of the model and determine the most important features in diagnosing PD. The present article uses Pearson Correlation Coefficients to understand the relationship between input features and the output. Input features with high correlation are selected and then classified by the Extreme Gradient Boosting, Light Gradient Boosting Machine, Gradient Boosting, and Bagging. Moreover, the weights in Hard Voting Ensemble Method are determined based on the performance of the mentioned classifiers. At the final stage, it uses SHAP to determine the most important features in PD diagnosis. The effectiveness of the proposed method is validated using 'Parkinson Dataset with Replicated Acoustic Features' from the UCI machine learning repository. It has achieved an accuracy of 85.42%. The findings demonstrate that the proposed method outperformed state-of-the-art approaches and can assist physicians in diagnosing Parkinson's cases. [ABSTRACT FROM AUTHOR]

Myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) is a severe condition with an uncertain origin and a dismal prognosis. There is presently no precise diagnostic test for ME/CFS, and the diagnosis is determined primarily by the presence of certain symptoms. The current study presents an explainable artificial intelligence (XAI) integrated machine learning (ML) framework that identifies and classifies potential metabolic biomarkers of ME/CFS. Metabolomic data from blood samples from 19 controls and 32 ME/CFS patients, all female, who were between age and body mass index (BMI) frequency-matched groups, were used to develop the XAI-based model. The dataset contained 832 metabolites, and after feature selection, the model was developed using only 50 metabolites, meaning less medical knowledge is required, thus reducing diagnostic costs and improving prognostic time. The computational method was developed using six different ML algorithms before and after feature selection. The final classification model was explained using the XAI approach, SHAP. The best-performing classification model (XGBoost) achieved an area under the receiver operating characteristic curve (AUCROC) value of 98.85%. SHAP results showed that decreased levels of alpha-CEHC sulfate, hypoxanthine, and phenylacetylglutamine, as well as increased levels of N-delta-acetylornithine and oleoyl-linoloyl-glycerol (18:1/18:2)[2], increased the risk of ME/CFS. Besides the robustness of the methodology used, the results showed that the combination of ML and XAI could explain the biomarker prediction of ME/CFS and provided a first step toward establishing prognostic models for ME/CFS. [ABSTRACT FROM AUTHOR]