Evidence map›Paper›PMID 40450589›Full record

ArticleAmyotrophic lateral sclerosis & frontotemporal degeneration2025

Differentiating upper- and lower motor neuron diseases using automated acoustic analysis.

Justin Truong, Leif Simmatis, Timothy Pommée, Agessandro Abrahao, Kerry Adams, Marvin Chum, Colleen O'Connell, Angela Genge, Sanjay Kalra, Benjamin Ritsma and 5 more

Abstract read
In one paragraph

Article in Amyotrophic lateral sclerosis & frontotemporal degeneration, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Justin TruongDepartment of Speech-Language Pathology, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Leif SimmatisDepartment of Speech-Language Pathology, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Timothy PomméeDepartment of Speech-Language Pathology, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.
Agessandro AbrahaoSunnybrook Research Institute, Toronto, Ontario, Canada.ORCID 0000-0003-1142-2842
Kerry AdamsAlberta Health Services, Kaye Edmonton Clinic ALS Programme, Edmonton, Alberta, Canada.
Marvin ChumFaculty of Health Sciences, McMaster University, Hamilton, Ontario, Canada.
Colleen O'ConnellDepartment of Rehabilitation, Stan Cassidy Centre for Rehabilitation, Horizon Health Network, Fredericton, New Brunswick, Canada.
Angela GengeDepartment of Neurology and Neurosurgery, Faculty of Medicine and Health Sciences, McGill University, Montreal, Quebec, Canada.
Sanjay KalraDivision of Neurology, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.
Benjamin RitsmaDepartment of Physical Medicine and Rehabilitation, Queen's University, Providence Care, Kingston, Ontario, Canada.
Kerri SchellenbergDivision of Neurology, Department of Medicine, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.ORCID 0000-0002-5820-2428
Christen ShoesmithDepartment of Clinical Neurological Sciences, London Health Sciences Centre, Western University, London, Ontario, Canada.
Lorne ZinmanDivision of Neurology, Department of Medicine, Sunnybrook Health Sciences and Harquail Centre for Neuromodulation, University of Toronto, Toronto, Ontario, Canada.
Gord JewettDepartment of Clinical Neurosciences, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Yana YunusovaDepartment of Speech-Language Pathology, Temerty Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

Funding

The development and validation of a novel tool for the assessment of bulbar dysfunction in ALSR01DC017291 · NIDCD · SUNNYBROOK RESEARCH INSTITUTE · PI JORDAN R GREEN, Yana Yunusova · 2018 to 2026
$3.6M
SPEECH MOVEMENT CLASSIFICATION FOR ASSESSING AND TREATING ALSR01DC013547 · NIDCD · MGH INSTITUTE OF HEALTH PROFESSIONS · PI GREEN, JORDAN R · 2014 to 2018
$3.2M
NIDCD NIH HHS R01 DC013547NIDCD NIH HHS R01 DC017291
6 · The paper itself

Abstract

objectiveMotor neuron diseases (MNDs) result in a spectrum of motor impairments, including considerable effects on speech function, which manifest as dysarthria-a motor speech disorder. Speech metrics are increasingly recognized as critical biomarkers with potential utility in disease diagnosis and phenotyping. This study aimed to (1) characterize acoustics of upper motor neuron (UMN) and lower motor neuron (LMN) dysarthria presentations in MNDs, and (2) identify relationships between bulbar disease severity scores and acoustic features, as these could collectively enable personalized approaches to management of these diseases.

methodsData from 16 individuals with primary lateral sclerosis (PLS) representing UMN disease, 14 individuals with spinal and bulbar muscular atrophy (SBMA) representing LMN disease, and 25 neurologically healthy individuals were analyzed. Clinical measures were also collected from PLS and SBMA groups. All participants were remotely recorded performing passage reading, rapid syllable repetition, and vowel phonation. Fifty-two acoustic features were extracted representing articulation, phonation, prosody, resonance, and overall speech timing. Features were compared using Kruskal-Wallis tests for between-group comparisons and Spearman correlations between acoustic features and clinical scores.

resultsArticulatory and prosodic features best differentiated PLS, SBMA and controls. Correlations were observed in the PLS group between the clinical score and various articulatory features, most notably those indexing tongue and jaw movements.

conclusionsOur study demonstrated that acoustic assessment could capture fingerprints of dysarthrias associated with PLS and SBMA. These findings also demonstrate the potential for remote speech assessment to characterize diverse dysarthria profiles and pave the way for creating ways for personalized disease management approaches in clinical care and trials.

Indexed as

DysarthriaMotor Neuron DiseaseSpeech AcousticsAdultAgedFemaleHumansMaleMiddle AgedSpeech Production MeasurementAcoustic analysisdysarthrialower motor neuronupper motor neuron

Identifiers

PMID40450589
PMCPMC12380423

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.