FLP: Factor lattice pattern-based automated detection of Parkinson's disease and specific language impairment using recorded speech.

Combinational majority voting Factor lattice pattern Parkinson's disease detection Specific language impairment Speech classification Vowel classification

Journal

Computers in biology and medicine
ISSN: 1879-0534
Titre abrégé: Comput Biol Med
Pays: United States
ID NLM: 1250250

Informations de publication

Date de publication:
20 Mar 2024
Historique:
received: 08 12 2023
revised: 18 02 2024
accepted: 09 03 2024
medline: 29 3 2024
pubmed: 29 3 2024
entrez: 28 3 2024
Statut: aheadofprint

Résumé

Timely detection of neurodevelopmental and neurological conditions is crucial for early intervention. Specific Language Impairment (SLI) in children and Parkinson's disease (PD) manifests in speech disturbances that may be exploited for diagnostic screening using recorded speech signals. We were motivated to develop an accurate yet computationally lightweight model for speech-based detection of SLI and PD, employing novel feature engineering techniques to mimic the adaptable dynamic weight assignment network capability of deep learning architectures. In this research, we have introduced an advanced feature engineering model incorporating a novel feature extraction function, the Factor Lattice Pattern (FLP), which is a quantum-inspired method and uses a superposition-like mechanism, making it dynamic in nature. The FLP encompasses eight distinct patterns, from which the most appropriate pattern was discerned based on the data structure. Through the implementation of the FLP, we automatically extracted signal-specific textural features. Additionally, we developed a new feature engineering model to assess the efficacy of the FLP. This model is self-organizing, producing nine potential results and subsequently choosing the optimal one. Our speech classification framework consists of (1) feature extraction using the proposed FLP and a statistical feature extractor; (2) feature selection employing iterative neighborhood component analysis and an intersection-based feature selector; (3) classification via support vector machine and k-nearest neighbors; and (4) outcome determination using combinational majority voting to select the most favorable results. To validate the classification capabilities of our proposed feature engineering model, designed to automatically detect PD and SLI, we employed three speech datasets of PD and SLI patients. Our presented FLP-centric model achieved classification accuracy of more than 95% and 99.79% for all PD and SLI datasets, respectively. Our results indicate that the proposed model is an accurate alternative to deep learning models in classifying neurological conditions using speech signals.

Sections du résumé

BACKGROUND BACKGROUND
Timely detection of neurodevelopmental and neurological conditions is crucial for early intervention. Specific Language Impairment (SLI) in children and Parkinson's disease (PD) manifests in speech disturbances that may be exploited for diagnostic screening using recorded speech signals. We were motivated to develop an accurate yet computationally lightweight model for speech-based detection of SLI and PD, employing novel feature engineering techniques to mimic the adaptable dynamic weight assignment network capability of deep learning architectures.
MATERIALS AND METHODS METHODS
In this research, we have introduced an advanced feature engineering model incorporating a novel feature extraction function, the Factor Lattice Pattern (FLP), which is a quantum-inspired method and uses a superposition-like mechanism, making it dynamic in nature. The FLP encompasses eight distinct patterns, from which the most appropriate pattern was discerned based on the data structure. Through the implementation of the FLP, we automatically extracted signal-specific textural features. Additionally, we developed a new feature engineering model to assess the efficacy of the FLP. This model is self-organizing, producing nine potential results and subsequently choosing the optimal one. Our speech classification framework consists of (1) feature extraction using the proposed FLP and a statistical feature extractor; (2) feature selection employing iterative neighborhood component analysis and an intersection-based feature selector; (3) classification via support vector machine and k-nearest neighbors; and (4) outcome determination using combinational majority voting to select the most favorable results.
RESULTS RESULTS
To validate the classification capabilities of our proposed feature engineering model, designed to automatically detect PD and SLI, we employed three speech datasets of PD and SLI patients. Our presented FLP-centric model achieved classification accuracy of more than 95% and 99.79% for all PD and SLI datasets, respectively.
CONCLUSIONS CONCLUSIONS
Our results indicate that the proposed model is an accurate alternative to deep learning models in classifying neurological conditions using speech signals.

Identifiants

pubmed: 38547655
pii: S0010-4825(24)00364-0
doi: 10.1016/j.compbiomed.2024.108280
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

108280

Informations de copyright

Copyright © 2024 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Turker Tuncer (T)

Department of Digital Forensics Engineering, Technology Faculty, Firat University, Elazig, Turkey. Electronic address: turkertuncer@firat.edu.tr.

Sengul Dogan (S)

Department of Digital Forensics Engineering, Technology Faculty, Firat University, Elazig, Turkey. Electronic address: sdogan@firat.edu.tr.

Mehmet Baygin (M)

Department of Computer Engineering, Faculty of Engineering and Architecture, Erzurum Technical University, Erzurum, Turkey. Electronic address: mehmet.baygin@erzurum.edu.tr.

Prabal Datta Barua (PD)

School of Business (Information System), University of Southern Queensland, Australia. Electronic address: Prabal.Barua@usq.edu.au.

Elizabeth Emma Palmer (EE)

Centre of Clinical Genetics, Sydney Children's Hospitals Network, Randwick, 2031, Australia; School of Women's and Children's Health, University of New South Wales, Randwick, 2031, Australia. Electronic address: elizabeth.palmer@unsw.edu.au.

Sonja March (S)

School of Psychology and Counselling and Centre for Health Research, University of Southern Queensland, Springfield, Australia. Electronic address: Sonja.March@unisq.edu.au.

Edward J Ciaccio (EJ)

Department of Medicine, Columbia University Irving Medical Center, USA. Electronic address: ciaccio@columbia.edu.

Ru-San Tan (RS)

Department of Cardiology, National Heart Centre Singapore, Singapore; Duke-NUS Medical School, Singapore.

U Rajendra Acharya (UR)

School of Mathematics, Physics and Computing, University of Southern Queensland, Springfield, Australia; Centre for Health Research, University of Southern Queensland, Australia. Electronic address: Rajendra.Acharya@usq.edu.au.

Classifications MeSH