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ArticleFrontiers in psychiatry2025

Deeper insight into speech characteristics of patients at ultra-high risk using classification and explainability models.

Deok-Hee Kim-Dufor, Michel Walter, Marie-Odile Krebs, Yannis Haralambous, Philippe Lenca, Christophe Lemey

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Article in Frontiers in psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

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3citing papers in PubMed, 1 pooled it
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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Deok-Hee Kim-DuforLimics, Sorbonne Université, Université Sorbonne Paris-Nord, INSERM, Paris, France.
Michel WalterUnité de Recherche Clinique en Psychiatrie (URCP), Department of Psychiatry, Centre Hospitalier Universitaire (CHU) de Brest, Brest, France.
Marie-Odile KrebsUniversity of Paris, Groupe Hospitalier Universitaire de Paris (GHU)-Paris, Service Hospitalo-Universitaire, Sainte-Anne, Centre d'évaluation pour Jeunes Adultes et ADolescents (C'JAAD), Paris, France.
Yannis HaralambousIMT Atlantique, Lab-STICC, UMR CNRS 6285, Brest, France.
Philippe LencaDonnées, Modèles, Informations & Décisions (DECIDE), Department of LUSSI, Institut Mines-Télécom (IMT) Atlantique, Brest, France.
Christophe LemeyUnité de Recherche Clinique en Psychiatrie (URCP), Department of Psychiatry, Centre Hospitalier Universitaire (CHU) de Brest, Brest, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Peculiar use of language and even language deficits are one of the well-known signs of schizophrenia. Different language features analyzed using natural language processing and machine learning have been reported to differentiate patients at ultra-high risk for psychosis. However, it has not always been explained how, and to what extent, those linguistic markers allow the distinction of patients. This study aims to find relevant linguistic markers for classifying patients at ultra-high risk and explain how the detected markers contribute to the classification. Methods: The first consultations with a psychiatrist of 68 patients (15 not-at-risk patients, 45 at-risk patients, and 8 patients with first episode psychosis) were recorded, transcribed verbatim, and annotated for analyses using natural language processing. A gradient-boosted decision tree algorithm was tested to evaluate its potential to correctly classify three categories of patients and find relevant linguistic markers at the level of lexical richness, semantic coherence, speech disfluency, and syntactic complexity. The Synthetic Minority Oversampling Technique was used to handle imbalanced data, and the SHapley Additive exPlanations (SHAP) values were computed to measure feature importance and each feature's contributions to the classification. Results: The model yielded good performance, that is, 0.82 accuracy, 0.82 F2-score, 0.85 precision, 0.82 recall, and 0.86 ROC-AUC score, with four linguistic variables that concern weak coherence, the use of "I," and filled pauses. Discussion: The findings in this study suggest that weak coherence play a key role in classification. No significant differences in the use of "I" and filled pauses were found between groups using a statistical test, but an explainability model showed its different contributions. The contribution of each linguistic feature to the classification by patient group provided deeper insight into linguistic manifestations of each patient group and their subtle differences, which could help better analyze and understand patients' language behaviors.

Indexed as

natural language processingSHAP valuesSMOTEspoken languageUHR patientsXGBoost

Identifiers

PMID40589653
PMCPMC12206705

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