Evidence map›Paper›PMID 42798815›Full record

ArticleBrain communications2026

Artificial intelligence-based speech error detection to differentiate primary progressive aphasia variants.

Jet M J Vonk, Jiachen Lian, G Lynn Kurteff, Cheol J Cho, Giada Antonicelli, Zoe Ezzes, Lisa D Wauters, Willa Keegan-Rodewald, Diana Alejandra Rodriguez, Nina Dronkers and 5 more

Abstract read
In one paragraph

Article in Brain communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Jet M J VonkEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.ORCID https://orcid.org/0000-0002-1808-8843
Jiachen LianDepartment of Electrical Engineering and Computer Sciences, University of California Berkeley, Berkeley, CA 94720, USA.
G Lynn KurteffEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.ORCID https://orcid.org/0000-0001-5800-546X
Cheol J ChoDepartment of Electrical Engineering and Computer Sciences, University of California Berkeley, Berkeley, CA 94720, USA.
Giada AntonicelliEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.ORCID https://orcid.org/0000-0002-4847-7612
Zoe EzzesSchool of Speech, Language, and Hearing Sciences, San Diego State University, San Diego, CA 92182, USA.ORCID https://orcid.org/0000-0001-7118-0502
Lisa D WautersDepartment of Speech, Language, and Hearing Sciences, The University of Texas at Austin, Austin, TX 78712, USA.
Willa Keegan-RodewaldEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.
Diana Alejandra RodriguezEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.
Nina DronkersDepartment of Psychology, University of California Berkeley, Berkeley, CA 94704, USA.
Maya L HenryDepartment of Speech, Language, and Hearing Sciences, The University of Texas at Austin, Austin, TX 78712, USA.
Zachary A MillerEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.ORCID https://orcid.org/0000-0002-5991-3053
Maria Luisa MandelliEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.
Gopala K AnumanchipalliDepartment of Electrical Engineering and Computer Sciences, University of California Berkeley, Berkeley, CA 94720, USA.
Maria Luisa Gorno-TempiniEdward and Pearl Fein Memory and Aging Center, Department of Neurology, University of California San Francisco, San Francisco , CA 94158, USA.

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
Progressive Aphasia Cognition Anatomy and ProgressionR01NS050915 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARIA LUISA GORNO TEMPINI · 2004 to 2026
$11.0M
An automated machine learning approach to language changes in Alzheimer’s disease and frontotemporal dementia across Latino and English-speaking populationsR01AG075775 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MARIA LUISA GORNO TEMPINI, Adolfo Martin Garcia · 2023 to 2026
$7.2M
Digital speech markers for early detection of Alzheimer’s disease in a longitudinal racially and ethnically diverse cohortRF1AG091509 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VONK, JET M.J. · 2025 to 2025
$4.6M
Training program in the neurology of language and neurodegenerative aphasiasK24DC015544 · NIDCD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GORNO TEMPINI, MARIA LUISA · 2016 to 2025
$1.9M
Preclinical markers of Alzheimer's disease using psycholinguistic semantic measuresR00AG066934 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI VONK, JET M.J. · 2022 to 2024
$1.2M
NIA NIH HHS P01 AG019724NIA NIH HHS R00 AG066934NIA NIH HHS R01 AG075775NIA NIH HHS RF1 AG091509NIDCD NIH HHS K24 DC015544NINDS NIH HHS R01 NS050915
6 · The paper itself

Abstract

Artificial intelligence-based approaches to speech analysis have the potential to assist with objective speech error analysis in aphasia but off-the shelf tools often fail to detect speech errors due to prioritizing 'fluent transcription'. Speech production errors (dysfluencies) are hallmark diagnostic features of the nonfluent and logopenic variants of primary progressive aphasia, yet they can be challenging to detect and characterize even by expert clinicians. This study aimed to evaluate whether the novel automated lightweight Scalable Speech Dysfluency Modeling system, specifically designed to detect dysfluencies, could accurately distinguish primary progressive aphasia variants using voice recordings of individuals reading a brief passage. Participants included a total of 104 individuals, 40 with non-fluent primary progressive aphasia and 40 with logopenic primary progressive aphasia (matched on disease severity), and 24 healthy controls who read aloud the 'Grandfather Passage' as part of a widely used motor speech evaluation. We automatically extracted ten speech error (dysfluency) variables, including insertions, replacements, and deletions at both phoneme- and word-levels, and phoneme-level prolongations and repetitions. Group differences were assessed via ANOVAs controlling for age, education, and disease severity (Mini-Mental State Examination and Clinical Dementia Rating sum-of-boxes). To test clinical relevance, we performed correlation analyses with motor speech evaluation ratings provided by experienced speech-language pathologists (i.e. gold standard) within the non-fluent primary progressive aphasia group. Classification performance was assessed by training random forest and XGBoost machine-learning models including 5-fold cross-validation. All individuals read the entire passage in less than five minutes. The lightweight Scalable Speech Dysfluency Modeling system detected 8 of the 10 predefined dysfluency features at sufficient frequency to include them in subsequent analyses. All eight features distinguished primary progressive aphasia from controls (

Indexed as

automated speech analysisfrontotemporal dementialanguagemotor speechspeech biomarkers

Identifiers

PMID42798815
PMCPMC13613221

What OpenQuestion holds

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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.