Evidence map›Paper›PMID 40796584›Full record

ArticleScientific reports2025

Application of machine learning and temporal response function modeling of EEG data for differential diagnosis in primary progressive aphasia.

Heather Dial, Lokesha S Pugalenthi, G Nike Gnanateja, Junyi Jessy Li, Maya L Henry

Abstract read
In one paragraph

Article in Scientific reports, 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

What it found

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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

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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

5 authors.

Heather Dial *Department of Communication Sciences and Disorders, University of Houston, 3871 Holman St, Houston, TX, 77204, USA. hrdial@central.uh.edu.
Lokesha S Pugalenthi *Department of Electrical and Computer Engineering, Rice University, 6100 Main Street MS 366, Houston, TX, 77005, USA.
G Nike GnanatejaDepartment of Communication Sciences and Disorders, University of Wisconsin-Madison, 1975 Willow Drive, Madison, WI, 53706, USA.
Junyi Jessy LiDepartment of Linguistics, The University of Texas at Austin Dell Medical School, 305 E 23rd St Suite 4.304, Austin, TX, 78712, USA.
Maya L HenryDepartment of Speech, Language, and Hearing Sciences, The University of Texas at Austin, 2504a Whitis Ave a1100, Austin, TX, 78712, USA.

Funding

Establishing Evidence-based Treatment for Speech and Language in Primary Progressive AphasiaR01DC016291 · NIDCD · UNIVERSITY OF TEXAS AT AUSTIN · PI HENRY, MAYA · 2017 to 2021
$3.3M
Rehabilitation of speech and language in primary progressive aphasiaR03DC013403 · NIDCD · UNIVERSITY OF TEXAS AT AUSTIN · PI HENRY, MAYA · 2014 to 2016
$565k
Investigating Neural Signatures of Rehabilitation in Primary Progressive AphasiaF32DC016812 · NIDCD · UNIVERSITY OF TEXAS AT AUSTIN · PI DIAL, HEATHER R · 2018 to 2020
$192k
NIDCD NIH HHS F32 DC016812NIDCD NIH HHS R01 DC016291NIDCD NIH HHS R03 DC013403NIH/NIDCD F32 DC016812-01
6 · The paper itself

Abstract

Primary progressive aphasia (PPA) is a neurodegenerative syndrome characterized by progressive decline in speech and/or language. There are three PPA subtypes with distinct speech-language profiles. Early diagnosis is essential for optimal provision of care but differential diagnosis by PPA subtype can be difficult and time consuming. We investigated the diagnostic utility of a novel electroencephalography (EEG)-based biomarker in conjunction with machine learning. Individuals with semantic, logopenic, or nonfluent/agrammatic variant PPA and healthy controls (n = 10 per group) listened to a continuous narrative while EEG responses were recorded. The speech envelope and linguistic features representing core language processes were extracted from the narrative speech and temporal response function (TRF) modeling was used to estimate the neural responses to these features. Although TRF modeling has shown promise for clinical applications, research is lacking regarding its diagnostic utility in populations like PPA. This study sought to provide preliminary evidence to address this gap. The resulting TRFs for channel Cz were used as input to machine learning algorithms for classification of PPA vs. healthy controls, three-way classification by PPA subtype, classification of a single PPA subtype relative to the other two (e.g., semantic vs. logopenic/nonfluent variant), and pairwise classification by PPA subtype. F1 scores were highest for the latter tasks (F1's from 0.73 to 0.74), with better-than-chance classification in all tasks. Additional analyses determined that the TRF beta weights significantly improved classification over preprocessed EEG waveforms alone for all but one task (PPA vs. healthy controls). Our preliminary findings demonstrate the potential utility of this approach for differential diagnosis of PPA, warranting further investigation.

Indexed as

Aphasia, Primary ProgressiveElectroencephalographyMachine LearningAgedDiagnosis, DifferentialFemaleHumansMaleMiddle AgedDifferential diagnosisElectroencephalographyMachine learningNatural language processingPrimary progressive aphasiaTemporal response function

Identifiers

PMID40796584
PMCPMC12344008

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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.