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RESEARCH PAPER ANALYSIS

Use of machine learning and voice for multiclass classification of Parkinson's disease, chronic obstructive pulmonary disease, and healthy controls.

AI interpretation is pending for this paper.

PMID42156531
JournalScientific reports
Publication Date2026-05-19
Ingested2026-05-20 10:30 PM
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ABSTRACT

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Parkinson's disease (PD) and chronic obstructive pulmonary disease (COPD) are prevalent conditions with substantial impact on quality of life and health care systems. Both disorders affect voice production through different physiological mechanisms, yet neither condition has a widely adopted objective biomarker for routine clinical use. Voice analysis has emerged as a non-invasive digital biomarker candidate, but existing studies have largely focused on binary classification within a single disorder or language. This study aimed to evaluate whether an unified multiclass machine learning (ML) framework applied to sustained vowel "a" phonation can discriminate between PD, COPD, and healthy controls (HC) across linguistically distinct cohorts. Sustained vowel recordings were analyzed from Swedish speaking individuals with COPD and HC, and English-speaking individuals with PD and HC, collected under comparable mobile recording conditions. Acoustic features included baseline voice measures and Mel Frequency Cepstral Coefficients. A soft voting ML framework integrating support vector machine, random forest, CatBoost, and light gradient boosting classifiers was trained using nested cross validation with hyperparameter optimization. Data were partitioned at the participant level into a development cohort and an independent test cohort. Model performance was evaluated using accuracy, macro averaged precision, recall, F1 score, receiver operating characteristic analysis, and confusion matrices. Model interpretability was assessed using Shapley additive explanations and vowel space analysis. The final soft voting classifier achieved robust multiclass discrimination on the participant disjoint independent test set, with an overall accuracy of 0.842 and a macro averaged F1 score of 0.839. Classification performance differed across groups, with the highest performance observed for PD, intermediate performance for HC, and lower performance for COPD. Misclassifications occurred primarily between HC and COPD, while confusion between PD and COPD was minimal. Feature attribution analysis revealed class dependent relevance patterns, and vowel space analysis demonstrated subtle but consistent group level differences. These findings demonstrate the feasibility of using an explainable soft voting machine learning framework applied to sustained vowel phonation to distinguish between neurologically and respiratory driven voice impairments across linguistic contexts. The study supports voice as a promising digital biomarker modality for multiclass clinical discrimination using mobile recordings.

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B, Biointerfaces 86.0 13 Neuroprotective roles of klotho: Molecular pathways and therapeutic implications for cognitive health in neurological and psychiatric diseases. Experimental physiology 84.0 14 Flavonoid Rutin Reduces Intestinal Inflammation in an Experimental Model of Parkinson's Disease. Neurotoxicity research 70.0 15 Nanostructured Lipid Carriers Enhance Brain Delivery and Antioxidant Efficacy of a Small-Molecule MAO B Inhibitor for Neurodegenerative Disease Therapy. Molecular pharmaceutics 78.0 16 Pathophysiological Role of the Gut Brain Axis in Parkinson's Disease: From Microbial Metabolites and Intestinal Permeability to Central Neuroinflammation. Current neurovascular research 86.0 17 Parkinson's Disease: From Metabolism to Genetics-A Comprehensive Review. Current issues in molecular biology 86.0 18 Navigating the cholesterol maze: Key insights on use of statins in neurodegenerative disorders. Neuroprotection (Chichester, England) 76.0 19 Integrative network pharmacology delineates dual GPCR and non-GPCR mechanisms of blended and individual Taikong Blue lavender and Pingyin rose essential oils in neurodegenerative and psychiatric disorders. Computers in biology and medicine 65.0 20 Models of neuroprotection in Parkinson's disease: Exploring cellular, molecular, and microenvironmental targets. Experimental neurology 78.0 21 Hyaluronic acid: emerging roles and biomaterial innovations in Alzheimer's and Parkinson's disease therapy. Frontiers in pharmacology 75.2 22 Molecular mechanisms underlying Parkinson's disease and role of phytochemicals, α-synuclein, sirtuins, and incretin mimetics in potential therapy. Frontiers in pharmacology 75.0 23 Lipid droplets in neurodegenerative diseases: pathological drivers and therapeutic vulnerabilities. Cell death discovery 82.0 24 Brain-gut-microbiota axis: a review on the bidirectional regulatory mechanisms between gut microbiota and brain and their disease interactions. Frontiers in microbiology 74.0 25 Long non-coding RNAs in neurodegenerative diseases - Molecular mechanisms, liquid biopsy biomarkers, and therapeutic targets: A review. Biomolecules & biomedicine 84.0 26 Neurosyphilis and Parkinsonism: Overlapping Pathophysiology and Emerging Therapeutic Insights. Current neurovascular research 76.0 27 Molecular biochemistry of soluble epoxide hydrolase in lipid mediator pathways and neuroinflammatory responses. The Journal of steroid biochemistry and molecular biology 82.0 28 Multifaceted role of CNPY2 beyond ER stress: Disease implications and therapeutic potential. Cell stress 83.3 29 Neuroprotective Role of Exercise-based Physiotherapy Combined with Pharmacological Agents in Parkinson's Disease. Central nervous system agents in medicinal chemistry 64.0 30 Distinct metabolomic and proteomic signatures in Parkinson's disease patients with REM sleep behavior disorder. Signal transduction and targeted therapy 84.0 31 HMGB1-mediated neuroinflammation: molecular mechanisms and emerging therapeutic approaches. Inflammopharmacology 78.0 32 Beyond acid-base dyshomeostasis: Dynamic instability of neuronal lysosomal pH as a pathogenic mechanism and therapeutic target in neurological diseases. Biochemical pharmacology 88.0
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