Evidence map›Paper›PMID 40658049›Full record

ArticlePsychiatry and clinical neurosciences2025

Plasma circulating microRNAs and symptoms of depression: Results from a population-based study.

Midas M Kuilman, Tim Finke, M Arfan Ikram, Annemarie I Luik, Alexander Neumann, Charlotte A M Cecil, Mohsen Ghanbari

Abstract read
In one paragraph

Article in Psychiatry and clinical neurosciences, 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
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

7 authors.

Midas M KuilmanDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID https://orcid.org/0009-0000-1562-7541
Tim FinkeDepartment of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID https://orcid.org/0009-0000-1796-6133
M Arfan IkramDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.
Annemarie I LuikDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0001-7517-197X
Alexander NeumannDepartment of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, The Netherlands.
Charlotte A M CecilDepartment of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, The Netherlands.
Mohsen GhanbariDepartment of Child and Adolescent Psychiatry, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID https://orcid.org/0000-0002-9476-7143

Funding

Alzheimer Nederland WE.03-2021-10Erasmus MC Fellowship EMCF20213European Research Council 101039672European Union's Horizon 2020 Research and Innovation Programme 848158European Union's Horizon Europe Research and Innovation Programme 101057529
6 · The paper itself

Abstract

backgroundDepression is a complex mental disorder with a multifactorial etiology. Recent research has highlighted the potential of microRNAs (miRNAs) as novel biomarkers and their involvement in the molecular pathways underlying depression; yet, these studies often focus on limited clinical samples and specific subsets of miRNAs. Here we aimed to explore plasma miRNA expression profiles associated with depressive symptoms in a population-based study of middle-aged and older adults.

methodsWe analyzed the levels of 591 circulating miRNAs well-expressed in plasma samples of 2,703 participants of the Rotterdam Study. The Center for Epidemiologic Studies Depression Scale was used to assess depressive symptoms in these participants. Negative-binomial regression models were employed to explore the relationship between individual miRNA levels and depressive symptoms, adjusting for potential confounders including age, sex, BMI, and other factors.

resultsOur analysis suggests 38 circulating miRNAs to be potentially associated with depressive symptoms (P < 0.05). Although these miRNAs did not survive multiple testing correction, our subsequent in silico analysis of their target genes suggests involvement in neural and psychiatric pathways, as well as enrichment for associations with depressive symptoms based on previous genome-wide association studies.

conclusionsThis study proposes several circulating miRNAs that may be associated with depressive symptoms within the general population. Our follow-up analyses indicate that the miRNAs with the largest effect estimates were potentially involved in neurological and psychiatric processes, warranting further investigation into their potential role in the biological mechanisms of depression. These results provide preliminary insights and should be considered exploratory and hypothesis-generating, warranting validation in future studies with larger and independent cohorts.

Indexed as

Circulating MicroRNADepressionAgedBiomarkersFemaleHumansMaleMiddle AgedNetherlandsBiomarkersCirculating MicroRNAbiomarkersdepressionMicroRNAspopulation‐based study

Identifiers

PMID40658049
PMCPMC12498121

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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.