Evidence map›Paper›PMID 38332015›Full record

ArticleNeuropsychopharmacology : official publication of the American College of Neuropsychopharmacology2024

White and gray matter alterations in bipolar I and bipolar II disorder subtypes compared with healthy controls - exploring associations with disease course and polygenic risk.

Katharina Thiel, Hannah Lemke, Alexandra Winter, Kira Flinkenflügel, Lena Waltemate, Linda Bonnekoh, Dominik Grotegerd, Katharina Dohm, Tim Hahn, Katharina Förster and 23 more

Open access · hybridAbstract read
In one paragraph

Article in Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
4.2field-weighted citation impact, top 5% of its field
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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
  2. Differential impact of manic versus depressive episode recurrence on longitudinal gray matter volume changes in bipolar disorder.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
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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

33 authors at 8 institutions in 1 country.

Katharina Thiel *Institute for Translational Psychiatry, University of Münster, Münster, Germany.
Hannah Lemke *Institute for Translational Psychiatry, University of Münster, Münster, Germany.ORCID http://orcid.org/0000-0001-7117-2908
Alexandra WinterInstitute for Translational Psychiatry, University of Münster, Münster, Germany.ORCID http://orcid.org/0000-0003-3759-1425
Kira FlinkenflügelInstitute for Translational Psychiatry, University of Münster, Münster, Germany.
Lena WaltemateInstitute for Translational Psychiatry, University of Münster, Münster, Germany.
Linda BonnekohInstitute for Translational Psychiatry, University of Münster, Münster, Germany.
Dominik GrotegerdInstitute for Translational Psychiatry, University of Münster, Münster, Germany.ORCID http://orcid.org/0000-0001-8718-0128
Katharina DohmInstitute for Translational Psychiatry, University of Münster, Münster, Germany.
Tim HahnInstitute for Translational Psychiatry, University of Münster, Münster, Germany.ORCID http://orcid.org/0000-0001-6541-3795
Katharina FörsterClinical Psychology and Behavioral Neuroscience, Faculty of Psychology, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0002-3041-9246
Philipp KanskeClinical Psychology and Behavioral Neuroscience, Faculty of Psychology, Technische Universität Dresden, Dresden, Germany.ORCID http://orcid.org/0000-0003-2027-8782
Jonathan ReppleInstitute for Translational Psychiatry, University of Münster, Münster, Germany.
Nils OpelInstitute for Translational Psychiatry, University of Münster, Münster, Germany.ORCID http://orcid.org/0000-0003-4749-3298
Ronny RedlichInstitute for Translational Psychiatry, University of Münster, Münster, Germany.
Friederike DavidInstitute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0001-9521-5669
Andreas J ForstnerInstitute of Human Genetics, University of Bonn, School of Medicine & University Hospital Bonn, Bonn, Germany.ORCID http://orcid.org/0000-0002-1876-6368
Frederike SteinDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Katharina BroschDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-0526-8095
Florian Thomas-OdenthalDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
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 http://orcid.org/0000-0003-2485-2374
Andreas JansenDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Stephanie H WittCentral Institute of Mental Health, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.ORCID http://orcid.org/0000-0002-1571-1468
Till F M AndlauerDepartment of Neurology, Klinikum rechts der Isar, School of Medicine, Technical University of Munich, Munich, Germany.ORCID http://orcid.org/0000-0002-2917-5889
Andrea PfennigDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, TU Dresden University of Technology, Dresden, Germany.
Michael BauerDepartment of Psychiatry and Psychotherapy, Faculty of Medicine, TU Dresden University of Technology, Dresden, Germany.
Igor NenadićDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.ORCID http://orcid.org/0000-0002-0749-7473
Tilo KircherDepartment of Psychiatry and Psychotherapy, University of Marburg, Marburg, Germany.
Susanne MeinertInstitute for Translational Psychiatry, University of Münster, Münster, Germany.ORCID http://orcid.org/0000-0003-2177-7161
Udo DannlowskiInstitute for Translational Psychiatry, University of Münster, Münster, Germany. udo.dannlowski@uni-muenster.de.
University of Münster · DEPhilipps University of Marburg · DETechnische Universität Dresden · DEUniversity of Bonn · DEGoethe University Frankfurt · DEHalle Institute for Economic Research · DEHeidelberg University · DETUM Klinikum · DE

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) DA1151/5-1Deutsche Forschungsgemeinschaft (German Research Foundation) DA1151/5-2Deutsche Forschungsgemeinschaft (German Research Foundation) DA1151/6-1Deutsche Forschungsgemeinschaft (German Research Foundation) HA7070/2-2Deutsche Forschungsgemeinschaft (German Research Foundation) JA1890/7-1Deutsche Forschungsgemeinschaft (German Research Foundation) JA1890/7-2Deutsche Forschungsgemeinschaft (German Research Foundation) KI588/14-1Deutsche Forschungsgemeinschaft (German Research Foundation) KI588/15-1Deutsche Forschungsgemeinschaft (German Research Foundation) KI588/17-1Deutsche Forschungsgemeinschaft (German Research Foundation) WI3439/3-1Deutsche Forschungsgemeinschaft (German Research Foundation) WI3439/3-2
6 · The paper itself

Abstract

Patients with bipolar disorder (BD) show alterations in both gray matter volume (GMV) and white matter (WM) integrity compared with healthy controls (HC). However, it remains unclear whether the phenotypically distinct BD subtypes (BD-I and BD-II) also exhibit brain structural differences. This study investigated GMV and WM differences between HC, BD-I, and BD-II, along with clinical and genetic associations. N = 73 BD-I, n = 63 BD-II patients and n = 136 matched HC were included. Using voxel-based morphometry and tract-based spatial statistics, main effects of group in GMV and fractional anisotropy (FA) were analyzed. Associations between clinical and genetic features and GMV or FA were calculated using regression models. For FA but not GMV, we found significant differences between groups. BD-I patients showed lower FA compared with BD-II patients (p

Indexed as

Bipolar DisorderWhite MatterAnisotropyBrainCerebral CortexGray MatterHumans

Identifiers

PMID38332015
PMCPMC10948847
OpenAlexW4391650178

What OpenQuestion holds

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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.