Evidence map›Paper›PMID 36907597›Full record

ArticleNeuropsychopharmacology reports2023

Serum soluble triggering receptor expressed on myeloid cells-2 was not altered by rTMS in patients with treatment-resistant depression.

Hiroshi Tateishi, Jun Matsushima, Hiroko Kunitake, Yoshiomi Imamura, Yutaka Kunitake, Toru Murakawa, Seiji Mawatari, Ryohei Kojima, Yuka Fujii, Jun Kikuchi and 8 more

Open access · goldAbstract read
In one paragraph

Article in Neuropsychopharmacology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

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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

18 authors at 2 institutions in 1 country.

Hiroshi TateishiDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.ORCID 0000-0002-6679-7150
Jun MatsushimaDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Hiroko KunitakeDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Yoshiomi ImamuraDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Yutaka KunitakeDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Toru MurakawaDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Seiji MawatariDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Ryohei KojimaDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Yuka FujiiDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Jun KikuchiDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Junko FukuchiDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Yuta SakemuraDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Takumi ShiraishiDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Chika NagahamaDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Toshihiko MaekawaDepartment of Neuropsychiatry, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Toyoko AsamiDepartment of Rehabilitation Medicine, Saga University Hospital, Saga, Japan.
Yoshito MizoguchiDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Akira MonjiDepartment of Psychiatry, Faculty of Medicine, Saga University, Saga, Japan.
Saga University · JPKyushu University · JP

Funding

Japan Society for the Promotion of Science JP17K10307
6 · The paper itself

Abstract

aimRepetitive transcranial magnetic stimulation (rTMS) is one of the most effective and minimally invasive treatments for treatment-resistant depression (TRD). However, the mechanism underlying the therapeutic effects of rTMS in patients with TRD remains unclear. In recent years, the pathogenesis of depression has been closely associated with chronic inflammation and microglia are believed to play an important role in chronic inflammation. Triggering receptor expressed on myeloid cells-2 (TREM2) plays an important role in microglial neuroinflammatory regulation. In this study, we investigated the changes in peripheral soluble TREM2 (sTREM2) before and after rTMS treatment in patients with TRD.

methodsTwenty-six patients with TRD were enrolled in this frequency (10 Hz) rTMS study. Depressive symptoms, cognitive function, and serum sTREM2 concentrations were measured at baseline and the end of the 6-week rTMS treatment.

resultsThis study showed that rTMS ameliorated depressive symptoms and partially improved cognitive dysfunction in TRD. However, rTMS treatment did not alter serum sTREM2 levels.

conclusionsThis is the first sTREM2 study in patients with TRD who underwent rTMS treatment. These results suggest that serum sTREM2 may not be relevant for the mechanism underlying the therapeutic effect of rTMS in patients with TRD. Future studies should confirm the present findings using a larger patient sample and a sham rTMS procedure, as well as CSF sTREM2. Furthermore, a longitudinal study should be conducted to clarify the effects of rTMS on sTREM2 levels.

Indexed as

Depressive Disorder, Treatment-ResistantReceptors, ImmunologicTranscranial Magnetic StimulationBody Mass IndexCognitionDepressionFemaleHumansLongitudinal StudiesMaleMembrane GlycoproteinsMiddle AgedSmokingMembrane GlycoproteinsReceptors, ImmunologicTREM2 protein, humancognitive dysfunctionrepetitive transcranial magnetic stimulationtreatment-resistant depressiontriggering receptor expressed on myeloid cells-2

Identifiers

PMID36907597
PMCPMC10275288
OpenAlexW4323975069

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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.