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Automated Vowel Articulation Analysis in Connected Speech Among Progressive Neurological Diseases, Dysarthria Types, and Dysarthria Severities

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68407700%3A21230%2F23%3A00368477" target="_blank" >RIV/68407700:21230/23:00368477 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11110/23:10468629 RIV/00064165:_____/23:10468629

  • Result on the web

    <a href="https://doi.org/10.1044/2023_JSLHR-22-00526" target="_blank" >https://doi.org/10.1044/2023_JSLHR-22-00526</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1044/2023_JSLHR-22-00526" target="_blank" >10.1044/2023_JSLHR-22-00526</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Automated Vowel Articulation Analysis in Connected Speech Among Progressive Neurological Diseases, Dysarthria Types, and Dysarthria Severities

  • Original language description

    Purpose: Although articulatory impairment represents distinct speech characteristics in most neurological diseases affecting movement, methods allowing automated assessments of articulation deficits from the connected speech are scarce. This study aimed to design a fully automated method for analyzing dysarthriarelated vowel articulation impairment and estimate its sensitivity in a broad range of neurological diseases and various types and severities of dysarthria.Method: Unconstrained monologue and reading passages were acquired from 459 speakers, including 306 healthy controls and 153 neurological patients. The algorithm utilized a formant tracker in combination with a phoneme recognizer and subsequent signal processing analysis.Results: Articulatory undershoot of vowels was presented in a broad spectrum of progressive neurodegenerative diseases, including Parkinson's disease, progressive supranuclear palsy, multiple-system atrophy, Huntington's disease, essential tremor, cerebellar ataxia, multiple sclerosis, and amyotrophic lateral sclerosis, as well as in related dysarthria subtypes including hypokinetic, hyper kinetic, ataxic, spastic, flaccid, and their mixed variants. Formant ratios showed a higher sensitivity to vowel deficits than vowel space area. First formants of corner vowels were significantly lower for multiple-system atrophy than cerebellar ataxia. Second formants of vowels /a/ and /i/ were lower in ataxic compared to spastic dysarthria. Discriminant analysis showed a classification score of up to 41.0% for disease type, 39.3% for dysarthria type, and 49.2% for dysarthria severity. Algorithm accuracy reached an F-score of 0.77. Conclusions: Distinctive vowel articulation alterations reflect underlying pathophysiology in neurological diseases. Objective acoustic analysis of vowel articulation has the potential to provide a universal method to screen motor speech disorders.Supplemental Material: https://doi.org/10.23641/asha.23681529

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    60203 - Linguistics

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2023

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Speech Language and Hearing Research

  • ISSN

    1092-4388

  • e-ISSN

    1558-9102

  • Volume of the periodical

    66

  • Issue of the periodical within the volume

    8

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    22

  • Pages from-to

    2600-2621

  • UT code for WoS article

    001056733600004

  • EID of the result in the Scopus database

    2-s2.0-85166442092