Evidence map›Paper›PMID 39613917›Full record

ArticleMolecular psychiatry2025

Structural alterations as a predictor of depression - a 7-Tesla MRI-based multidimensional approach.

Gereon J Schnellbächer, Ravichandran Rajkumar, Tanja Veselinović, Shukti Ramkiran, Jana Hagen, Maria Collee, N Jon Shah, Irene Neuner

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 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

8 authors.

Gereon J SchnellbächerDepartment of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany.
Ravichandran RajkumarDepartment of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-5875-5316
Tanja Veselinović *Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-7906-6966
Shukti RamkiranDepartment of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany.ORCID 0000-0001-8253-1873
Jana HagenDepartment of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany.ORCID 0009-0008-2861-6719
Maria ColleeDepartment of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany.ORCID 0009-0000-4895-8021
N Jon ShahInstitute of Neuroscience and Medicine 4, INM-4, Forschungszentrum Jülich, Germany.
Irene Neuner *Department of Psychiatry, Psychotherapy and Psychosomatics, RWTH Aachen University, Aachen, Germany. ineuner@ukaachen.de.ORCID 0000-0002-5164-8873

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder (MDD) is a debilitating condition that is associated with changes in the default-mode network (DMN). Commonly reported features include alterations in gray matter volume (GMV), cortical thickness (CoT), and gyrification. A comprehensive examination of these variables using ultra-high field strength MRI and machine learning methods may lead to novel insights into the pathophysiology of depression and help develop a more personalized therapy. Cerebral images were obtained from 41 patients with confirmed MDD and 41 healthy controls, matched for age and gender, using a 7-T-MRI. DMN parcellation followed the Schaefer 600 Atlas. Based on the results of a mixed-model repeated measures analysis, a support vector machine (SVM) calculation followed by leave-one-out cross-validation determined the predictive ability of structural features for the presence of MDD. A consecutive permutation procedure identified which areas contributed to the classification results. Correlating changes in those areas with BDI-II and AMDP scores added an explanatory aspect to this study. CoT did not delineate relevant changes in the mixed model and was excluded from further analysis. The SVM achieved a good prediction accuracy of 0.76 using gyrification data. GMV was not a viable predictor for disease presence, however, it correlated in the left parahippocampal gyrus with disease severity as measured by the BDI-II. Structural data of the DMN may therefore contain the necessary information to predict the presence of MDD. However, there may be inherent challenges with predicting disease course or treatment response due to high GMV variance and the static character of gyrification. Further improvements in data acquisition and analysis may help to overcome these difficulties.

Indexed as

DepressionMajor Depressive DisorderAdultBrainCerebral CortexDefault Mode NetworkFemaleGray MatterHumansMagnetic Resonance ImagingMaleMiddle AgedSupport Vector Machine

Identifiers

PMID39613917
PMCPMC12092240

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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.