Evidence map›Paper›PMID 41807345›Full record

ArticleTranslational psychiatry2026

Multimodal EEG-fNIRS classification as a clinical tool for bipolar disorder diagnosis.

I Tahir, A Planat-Chrétien, A Bertrand, M Linder, C Dondé, R Sosnik, M Polosan

Abstract read
In one paragraph

Article in Translational psychiatry, 2026. 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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0citing papers in PubMed
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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

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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

7 authors.

I TahirUniv. Grenoble Alpes, CEA-Leti Minatec, Campus MINATEC, F-38000, Grenoble, France. ines.tahir@cea.fr.ORCID http://orcid.org/0009-0008-7261-7364
A Planat-ChrétienUniv. Grenoble Alpes, CEA-Leti Minatec, Campus MINATEC, F-38000, Grenoble, France.
A BertrandCentre Hospitalier Universitaire Grenoble Alpes, Service Hospitalo-Universitaire de Psychiatrie, F-38000, Grenoble, France.
M LinderSha'ar Menashe Mental Health Center, Sha'ar Menashe, Haifa, Israel.
C DondéUniv. Grenoble Alpes, Inserm U1216, Grenoble Institut de Neurosciences, CHU de Grenoble, F-38000, Grenoble, France.
R SosnikFaculty of Electrical and Electronics Engineering, Holon Institute of Technology (HIT), Holon, Israel.ORCID http://orcid.org/0000-0002-8582-349X
M PolosanUniv. Grenoble Alpes, Inserm U1216, Grenoble Institut de Neurosciences, CHU de Grenoble, F-38000, Grenoble, France.

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-11-INBS-0006Ministère de l'Enseignement Supérieur, de la Recherche, de la Science et de la Technologie (MESRST) PHC MAIMONIDE 2022_Projet N°46504UB
6 · The paper itself

Abstract

Bipolar disorder (BD) is a complex mood disorder characterized by recurrent depressive and manic/hypomanic episodes, accompanied by significant cognitive dysfunction and emotional dysregulation. Accurate and timely diagnosis, especially the differentiation between subtypes, remains a challenge due to overlapping symptoms, variable onset times for more specific symptoms (e.g., psychotic features), and the reliance on subjective assessments. This study examines the use of a multimodal approach combining electroencephalography (EEG) and functional near-infrared spectroscopy (fNIRS) to identify patterns of BD emotional dysregulation, aiming to enhance its diagnosis and subtype differentiation. The protocol employed an emotional visual task to evaluate the interference of emotional content on cognitive function. EEG data were collected using a whole-head cap, while fNIRS focused on hemodynamic changes in the frontal cortex. Furthermore, the feasibility of using a potential simplified, portable EEG-fNIRS system was explored by focusing the analysis on frontal regions. The cohort included BD patients [BP] of two main subtypes, and healthy controls [HC]. Behavioral analysis revealed significant performance differences between BP and HC groups. While EEG alone enabled groups' classification, integrating EEG and fNIRS improved accuracy by reducing misclassification rates. Although classification using only frontal EEG regions was slightly less accurate than the full-head cap, fNIRS integration ensured robust results, supporting the feasibility for a potential simplified system. These findings underscore the complementary strengths of EEG and fNIRS in capturing neural and vascular markers of emotional dysregulation in BD and support the development of multimodal diagnostic tools for BD.

Indexed as

Bipolar DisorderElectroencephalographyAdultCase-Control StudiesEmotionsFemaleFrontal LobeHumansMaleSpectroscopy, Near-Infrared

Identifiers

PMID41807345
PMCPMC13039831

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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.