Evidence map›Paper›PMID 39895596›Full record

ArticlePsychiatry and clinical neurosciences2025

Advancing treatment response prediction in first-episode psychosis: integrating clinical and electroencephalography features.

Livia Dominicus, Melissa Zandstra, Josephine Franse, Wim Otte, Arjan Hillebrand, Simone de Graaf, Karen Ambrosen, Birte Yding Glenthøj, Andrew Zalesky, Kirsten Borup Bojesen and 6 more

Abstract read
In one paragraph

Article in Psychiatry and clinical neurosciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

16 authors.

Livia DominicusDepartment of Psychiatry, University Medical Center Utrecht, Utrecht, The Netherlands.ORCID https://orcid.org/0000-0002-7241-7214
Melissa ZandstraDepartment of Psychiatry, University Medical Center Utrecht, Utrecht, The Netherlands.
Josephine FranseDepartment of Psychiatry, University Medical Center Utrecht, Utrecht, The Netherlands.
Wim OtteDepartment of Child Neurology, UMC Utrecht Brain Center, University Medical Center Utrecht, and Utrecht University, Utrecht, The Netherlands.
Arjan HillebrandAmsterdam Neuroscience, Brain Imaging, Amsterdam, The Netherlands.ORCID https://orcid.org/0000-0002-8508-3532
Simone de GraafDepartment of Psychiatry, University Medical Center Utrecht, Utrecht, The Netherlands.
Karen AmbrosenCenter for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Copenhagen University Hospital, Mental Health Center Glostrup, Glostrup, Denmark.
Birte Yding GlenthøjCenter for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Copenhagen University Hospital, Mental Health Center Glostrup, Glostrup, Denmark.
Andrew ZaleskyMelbourne Neuropsychiatry Centre, University of Melbourne, Melbourne, Victoria, Australia.
Kirsten Borup BojesenCenter for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Copenhagen University Hospital, Mental Health Center Glostrup, Glostrup, Denmark.ORCID https://orcid.org/0000-0002-7996-3154
Mikkel SørensenCenter for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Copenhagen University Hospital, Mental Health Center Glostrup, Glostrup, Denmark.
Floortje ScheepersDepartment of Psychiatry, University Medical Center Utrecht, Utrecht, The Netherlands.
Cornelis StamDepartment of Clinical Neurophysiology and MEG Center, Department of Neurology, Amsterdam Neuroscience, Vrije Universiteit Amsterdam, Amsterdam UMC, Amsterdam, The Netherlands.
Bob OranjeCenter for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Copenhagen University Hospital, Mental Health Center Glostrup, Glostrup, Denmark.
Bjorn EbdrupCenter for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Copenhagen University Hospital, Mental Health Center Glostrup, Glostrup, Denmark.
Edwin van DellenDepartment of Psychiatry, University Medical Center Utrecht, Utrecht, The Netherlands.

Funding

ZonMw 60-63600-98-711
6 · The paper itself

Abstract

aimsPrompt diagnosis and intervention are crucial for first-episode psychosis (FEP) outcomes, but predicting the response to antipsychotics remains challenging. We studied whether adding electroencephalography (EEG) characteristics improves clinical prediction models for treatment response and whether EEG-based predictors are influenced by initial treatment.

methodsWe included 115 antipsychotic-naïve patients with FEP. Positive and Negative Syndrome Scale (PANSS) and sociodemographic items were included as clinical features. Additionally, we analyzed resting-state EEG data (n = 45) for (relative) power, functional connectivity, and network organization. Treatment response, measured as change in PANSS positive subscale scores (∆PANSS+), was predicted using a random forest regression model. We analyzed whether the most predictive EEG characteristics were influenced after treatment.

resultsThe clinical model explained 12% variance in symptom reduction in the training set and 32% in the validation set. Including EEG variables in the model led to a nonsignificant increase of 2% (total 34%) explained variance in symptom reduction. High hallucination symptom scores and a more hierarchical organization of alpha band networks (tree hierarchy) were associated with ∆PANSS+ reduction. The tree hierarchy in the alpha band decreased after medication. EEG source analysis revealed that this change was driven by alterations in the degree and centrality of frontal and parietal nodes in the functional brain network.

conclusionsBoth clinical and EEG characteristics can inform treatment response prediction in patients with FEP, but the combined model may not be beneficial over a clinical model. Nevertheless, adding a more objective marker such as EEG could be valuable in selected cases.

Indexed as

Antipsychotic AgentsElectroencephalographyNerve NetOutcome Assessment, Health CarePsychotic DisordersSchizophreniaAdolescentAdultConnectomeFemaleHumansMaleYoung AdultAntipsychotic Agentselectroencephalographyfirst‐episode psychosismachine learningpredictiontreatment response

Identifiers

PMID39895596
PMCPMC11962345

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LicenceCC BY-NC-ND
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Registered trials

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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.