Evidence map›Paper›PMID 42057765›Full record

SynthesisNeuropsychopharmacology reports2026

Glutathione-Related Metabolite Levels and Enzyme Activities in Depression: A Systematic Review and Meta-Analysis.

Takahide Etani, Nobuaki Hondo, Sho Moriguchi, Kazunari Yoshida, Sotaro Moriyama, Koki Takahashi, Tahichi Moritake, Yumina Nakamura, Ryoma Kani, Shiori Honda and 7 more

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Neuropsychopharmacology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

17 authors.

Takahide EtaniKeio University Hospital, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0003-0027-2551
Nobuaki HondoDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0009-0000-2452-7841
Sho MoriguchiDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0001-7536-9708
Kazunari YoshidaDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-1965-9484
Sotaro MoriyamaDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0001-8142-5665
Koki TakahashiDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0009-0002-8890-9325
Tahichi MoritakeDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Yumina NakamuraDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Ryoma KaniPostgraduate Education Center Kameda Medical Center, Kamogawa-shi, Chiba, Japan.ORCID https://orcid.org/0009-0005-4540-445X
Shiori HondaDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.
Masataka WadaDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-3937-3619
Sakiko TsugawaDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0001-9974-316X
Yukino MoriNational Kohnodai Hospital Medical Center, Ichikawa-shi, Chiba, Japan.
Hikari SegawaNational Hospital Organizations Saitama Hospital, Wako-shi, Saitama, Japan.
Tony KakuDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0009-0000-4870-4021
Hiroyuki UchidaDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0002-0628-7036
Shinichiro NakajimaDepartment of Neuropsychiatry, Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan.ORCID https://orcid.org/0000-0003-4229-1910

Funding

Japan Agency for Medical Research and Development JP24wm0625302Japan Research Foundation for Clinical PharmacologyJapan Society for the Promotion of Science 18H02755Japan Society for the Promotion of Science 22H03002Naito FoundationTakeda Science FoundationWatanabe Foundation
6 · The paper itself

Abstract

Recently, an increasing number of studies have reported abnormal levels of glutathione (GSH)-related metabolites and enzyme activities in neuroimaging and peripheral samples in patients with depression, indicating abnormalities in the GSH cycle in patients with depression. However, the abnormalities in the GSH cycle have not been comprehensively investigated. Here, we conducted a systematic review and meta-analysis to compare the levels of GSH-related metabolites (GSH and GSH disulfide [GSSG]) and the activities of GSH-related enzymes (Glutathione-peroxidase [GPx], GSH reductase [GR], glutamate-cysteine ligase [GCL], GSH synthetase [GS], and GSH S-transferase [GST]) between patients with depression and healthy controls (HC). The search was performed with MEDLINE, Embase, and PsychINFO. The inclusion criteria were studies comparing levels of GSH-related metabolites and enzyme activities between patients with depression and HC. Standardized mean differences were calculated to assess group differences. Thirty studies met the eligibility criteria, which included 1019 patients and 947 HC. Our meta-analysis indicated significantly decreased activity of GPx in patients with depression compared with HC, while the levels of GSH and GR were not significantly different between the groups. Because no studies, or an insufficient number of studies, have been conducted on GSSG, GST, GCL, and GS, meta-analyses were not performed for these metabolites and enzyme activities. Our findings suggest that abnormal cycling of the GSH system, particularly decreased GPx activity, is involved in the pathophysiology of depression and may serve as a potential biomarker for this illness. Furthermore, given that no or insufficient studies have been conducted on GSSG, GST, GCL, and GS, this study highlights the need for further research to fully elucidate the GSH cycle in patients with depression.

Indexed as

DepressionGlutathioneGlutamate-Cysteine LigaseGlutathione PeroxidaseGlutathione ReductaseGlutathione SynthaseGlutathione TransferaseHumansGlutamate-Cysteine LigaseGlutathioneGlutathione PeroxidaseGlutathione ReductaseGlutathione SynthaseGlutathione Transferasedepressionglutathioneoxidative stresssystematic review and meta‐analysis

Identifiers

PMID42057765
PMCPMC13129703

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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.