Evidence map›Paper›PMID 39681629›Full record

Observational studyMolecular psychiatry2025

Electroconvulsive therapy-specific volume changes in nuclei of the amygdala and their relationship to long-term anxiety improvement in depression.

Yuzuki Ishikawa, Naoya Oishi, Yusuke Kyuragi, Momoko Hatakoshi, Jinichi Hirano, Takamasa Noda, Yujiro Yoshihara, Yuri Ito, Jun Miyata, Kiyotaka Nemoto and 13 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study 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
  2. Review
  3. 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

23 authors.

Yuzuki IshikawaDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID 0009-0007-6855-0147
Naoya OishiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan. noishi@kuhp.kyoto-u.ac.jp.ORCID 0000-0002-0778-3381
Yusuke KyuragiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Momoko HatakoshiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Jinichi HiranoDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Takamasa NodaDepartment of Psychiatry, National Center of Neurology and Psychiatry, Tokyo, Japan.
Yujiro YoshiharaDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Yuri ItoDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Jun MiyataDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID 0000-0003-1803-1975
Kiyotaka NemotoDepartment of Psychiatry, Institute of Medicine, University of Tsukuba, Ibaraki, Japan.ORCID 0000-0001-8623-9829
Yoshihisa FujitaDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hiroyuki IgarashiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Kento TakahashiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Shingo MurakamiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Hiroyuki KannoDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Yudai IzumiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.
Akihiro TakamiyaDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.ORCID 0000-0003-2985-6673
Junya MatsumotoDepartment of Pathology of Mental Diseases, National Institute of Mental Health, National Center of Neurology and Psychiatry, Tokyo, Japan.ORCID 0000-0003-4228-3208
Fumitoshi KodakaDepartment of Psychiatry, The Jikei University School of Medicine, Tokyo, Japan.
Kazuyuki NakagomeNational Center of Neurology and Psychiatry, Tokyo, Japan.
Masaru MimuraDepartment of Neuropsychiatry, Keio University School of Medicine, Tokyo, Japan.
Toshiya MuraiDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan.ORCID 0000-0001-6550-8188
Taro SuwaDepartment of Psychiatry, Graduate School of Medicine, Kyoto University, Kyoto, Japan. tarosuwa@kuhp.kyoto-u.ac.jp.

Funding

Japan Agency for Medical Research and Development (AMED) JP19dm0307102MEXT | Japan Society for the Promotion of Science (JSPS) 21H02849MEXT | Japan Society for the Promotion of Science (JSPS) 24K10678MEXT | Japan Society for the Promotion of Science (JSPS) 24K10808
6 · The paper itself

Abstract

Electroconvulsive therapy (ECT) is one of the most effective treatments for depression. ECT induces volume changes in the amygdala, a key center of anxiety. However, the clinical relevance of ECT-induced changes in amygdala volume remains uncertain. We hypothesized that nuclei-specific amygdala volumes and anxiety symptoms in depression could explain the clinical correlates of ECT-induced volume changes. To test this hypothesis, we enrolled patients with depression who underwent ECT (N = 20) in this multicenter observational study and collected MRI data at three time points: before and after treatment and a 6-month follow-up. Patients who received medication (N = 52), cognitive behavioral therapy (N = 63), or transcranial magnetic stimulation (N = 20), and healthy participants (N = 147) were included for comparison. Amygdala nuclei were identified using FreeSurfer and clustered into three subdivisions to enhance reliability and interpretability. Anxiety symptoms were quantified using the anxiety factor scores derived from the Hamilton Depression Rating Scale. Before treatment, basolateral and basomedial subdivisions of the right amygdala were smaller than those of healthy controls. The volumes of the amygdala subdivisions increased after ECT and decreased during the follow-up period, but the volumes at 6-month follow-up were larger than those observed before treatment. These volume changes were specific to ECT. Long-term volume changes in the right basomedial amygdala correlated with improvements in anxiety symptoms. Baseline volumes in the right basolateral amygdala correlated with long-term improvements in anxiety symptoms. These findings demonstrate that clinical correlates of ECT-induced amygdala volume changes are existent, but in a nucleus and symptom-specific manner.

Indexed as

AmygdalaAnxietyDepressionElectroconvulsive TherapyAdultAgedCognitive Behavioral TherapyFemaleHumansMagnetic Resonance ImagingMajor Depressive DisorderMaleMiddle AgedPsychiatric Status Rating ScalesTranscranial Magnetic StimulationTreatment Outcome

Identifiers

PMID39681629
PMCPMC12092276

What Socratic holds

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LicenceCC BY
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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 Socratic graph.