Evidence map›Paper›PMID 40948223›Full record

ArticleEuropean psychiatry : the journal of the Association of European Psychiatrists2025

Disease progression in bipolar disorder in relation to white matter microstructure: A comprehensive approach based on staging models.

Katharina Thiel, Kira Flinkenflügel, Dominik Grotegerd, Christoph Jurischka, Julia Hubbert, Tim Hahn, Elisabeth J Leehr, Hannah Meinert, Elisabeth Schrammen, Florian Thomas-Odenthal and 16 more

Abstract read
In one paragraph

Article in European psychiatry : the journal of the Association of European Psychiatrists, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

26 authors.

Katharina ThielInstitute for Translational Psychiatry, University of Münster, Münster, German.ORCID 0000-0001-8297-1094
Kira FlinkenflügelInstitute for Translational Psychiatry, University of Münster, Münster, German.ORCID 0000-0001-7738-5429
Dominik GrotegerdInstitute for Translational Psychiatry, University of Münster, Münster, German.
Christoph JurischkaInstitute for Translational Psychiatry, University of Münster, Münster, German.ORCID 0009-0006-9008-5758
Julia HubbertInstitute for Translational Psychiatry, University of Münster, Münster, German.
Tim HahnInstitute for Translational Psychiatry, University of Münster, Münster, German.
Elisabeth J LeehrInstitute for Translational Psychiatry, University of Münster, Münster, German.
Hannah MeinertInstitute for Translational Psychiatry, University of Münster, Münster, German.ORCID 0000-0002-2230-0966
Elisabeth SchrammenInstitute for Translational Psychiatry, University of Münster, Münster, German.
Florian Thomas-OdenthalDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.ORCID 0000-0003-4912-8307
Paula UsemannDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Lea TeutenbergDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Benjamin StraubeDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Nina AlexanderDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Hamidreza JamalabadiDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.ORCID 0000-0003-2485-2374
Andreas JansenDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Frederike SteinDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Michael BauerDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, TUD Dresden University of Technology, Dresden, Germany.ORCID 0000-0002-2666-859X
Andrea PfennigDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, TUD Dresden University of Technology, Dresden, Germany.
Eva MennigenDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, TUD Dresden University of Technology, Dresden, Germany.ORCID 0000-0001-5099-0274
Philipp KanskeClinical Psychology and Behavioral Neuroscience, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany.ORCID 0000-0003-2027-8782
Katharina FörsterClinical Psychology and Behavioral Neuroscience, Faculty of Psychology, TUD Dresden University of Technology, Dresden, Germany.
Igor NenadićDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.ORCID 0000-0002-0749-7473
Tilo KircherDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Susanne MeinertInstitute for Translational Psychiatry, University of Münster, Münster, German.
Udo DannlowskiInstitute for Translational Psychiatry, University of Münster, Münster, German.

Funding

Deutsche Forschungsgemeinschaft DA1151/10-1Deutsche Forschungsgemeinschaft DA1151/11-1Deutsche Forschungsgemeinschaft DA1151/5-1Deutsche Forschungsgemeinschaft DA1151/5-2Deutsche Forschungsgemeinschaft DA1151/6-1Deutsche Forschungsgemeinschaft DA1151/9-1Deutsche Forschungsgemeinschaft HA7070/2-2Deutsche Forschungsgemeinschaft KI588/14-1Deutsche Forschungsgemeinschaft KI588/14-2Deutsche Forschungsgemeinschaft KI588/15-1Deutsche Forschungsgemeinschaft KI588/17-1Deutsche Forschungsgemeinschaft NE2254/1-2Deutsche Forschungsgemeinschaft NE2254/3-1Deutsche Forschungsgemeinschaft NE2254/4-1Deutsche Forschungsgemeinschaft SFB/TRR 393, project grant no 521379614Hessisches Ministerium für Wissenschaft und Kunst LOEWE1/16/519/03/09.001(0009)/98Medizinische Fakultät, Westfälische Wilhelms-Universität Münster Dan3/022/22
6 · The paper itself

Abstract

backgroundBipolar disorder (BD) is assumed to follow a progressive course, conceptualized through staging models. It is unclear whether white matter (WM) microstructure abnormalities, central to BD pathophysiology, parallel this development throughout disease progression. This study explored the link between WM and disease progression in BD, using a comprehensive approach based on clinical staging models.

methodsThis cross-sectional diffusion tensor-imaging study included 153 BD patients and 153 healthy controls (HCs) matched for age, sex, and study site. Using tract-based spatial statistics (TBSS), we examined associations between WM integrity and three criteria: (1) number of manic episodes, (2) remission quality between episodes, and (3) inter-episode global functioning.

resultsAnalyses revealed significant fractional anisotropy (FA) differences between early and late stages of BD based on the number of manic episodes (

conclusionsResults indicated more severe WM disruptions in patients at advanced stages compared to earlier stages of the disease. While these findings may imply changes occurring with disease progression, the cross-sectional design cannot rule out that they instead reflect stable clinical subtypes of varying severity. The results highlight the clinical relevance of WM alterations and the need for longitudinal studies to better understand the neurobiology and complexity of BD.

Indexed as

Bipolar DisorderDisease ProgressionWhite MatterAdultCross-Sectional StudiesDiffusion Tensor ImagingFemaleHumansMaleMiddle Agedbipolar disorderdiffusion tensor imagingneuroprogressionstagingwhite matter microstructure

Identifiers

PMID40948223
PMCPMC12538178

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.