Evidence map›Paper›PMID 41036088›Full record

ArticleBrain, behavior, & immunity - health2025

Dysregulated miR-1246 and miR-1253 link inflammatory protein markers in plasma to major depressive disorder in female adolescents.

Kristine Johannessen, Dušan Braný, Dana Dvorská, Michaela Krivošová, Miloslav Oppa, Igor Ondrejka, Ján Strnádel, Nikola Ferencová, Ingrid Tonhajzerová, Zuzana Danková and 3 more

Abstract read
In one paragraph

Article in Brain, behavior, & immunity - health, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Trial
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

13 authors.

Kristine JohannessenExperimental and Molecular Psychiatry, Translational Neuropsychiatry Unit, Department of Clinical Medicine, Aarhus University, Palle Juul-Jensens Blvd 11, 8200, Aarhus, Denmark.
Dušan BranýBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Dana DvorskáBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Michaela KrivošováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Miloslav OppaPsychiatric Clinic, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, University Hospital Martin, Martin, Slovak Republic.
Igor OndrejkaPsychiatric Clinic, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, University Hospital Martin, Martin, Slovak Republic.
Ján StrnádelBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Nikola FerencováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Ingrid TonhajzerováPsychiatric Clinic, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, University Hospital Martin, Martin, Slovak Republic.
Zuzana DankováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Erika HalašováBiomedical Centre Martin, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Juraj MokrýDepartment of Pharmacology, Jessenius Faculty of Medicine in Martin, Comenius University in Bratislava, Martin, Slovak Republic.
Betina ElfvingExperimental and Molecular Psychiatry, Translational Neuropsychiatry Unit, Department of Clinical Medicine, Aarhus University, Palle Juul-Jensens Blvd 11, 8200, Aarhus, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Major depressive disorder (MDD) in adolescents is a prevalent psychiatric condition worldwide with severe consequences. Growing evidence shows that microRNAs (miRNAs) regulate many processes hypothesized to be involved in the pathogenesis of MDD including inflammation, suggesting their suitability as biomarkers. Still, more research is needed regarding miRNAs as biomarkers and the role of inflammation in adolescents with MDD. This study applied the NanoString nCounter technology to identify dysregulated miRNAs in plasma from hospitalized female adolescents with MDD compared to healthy controls, as well as before and after antidepressant treatment. A multiplexed immunoassay was also performed to assess the plasma levels of 27 inflammatory proteins. A total of 33 patients and 14 healthy controls were included in the study. miR-1246 and miR-1253 were downregulated in female adolescents with MDD compared to healthy controls, suggesting their potential as diagnostic biomarkers. Additionally, miR-496 was downregulated with treatment, indicating its potential as a prognostic biomarker. Moreover, increased levels of PDGF-BB and IL-7 were seen in adolescents with MDD compared to healthy controls, while IL-9 and MIP-1β levels decreased with antidepressant treatment. Finally, the expression of specific miRNAs were found to correlate with the levels of several inflammatory proteins. In summary, miR-1246, miR-1253, and miR-496 are suggested as potential diagnostic and prognostic biomarkers. Furthermore, this study contributes in more detail to our understanding of miRNAs, inflammation, and MDD in female adolescents.

Indexed as

BiomarkersFemale adolescentsInflammationMajor depressive disordermicroRNANanoString technology

Identifiers

PMID41036088
PMCPMC12482293

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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.