Evidence map›Paper›PMID 40473930›Full record

ArticleMolecular psychiatry2025

Differentially expressed transcripts associated with depressive symptoms during pregnancy and postpartum.

Richelle D Björvang, Maria Vrettou, Xabier Bujanda Cundin, Eugenio Del Prete, Joëlle Rüegg, Susanne Lager, Diego di Bernardo, Erika Comasco, Alkistis Skalkidou

Abstract read
In one paragraph

Article in Molecular psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

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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

9 authors.

Richelle D Björvang *Department of Women's and Children's Health, Uppsala University, 751 85, Uppsala, Sweden.
Maria Vrettou *Department of Women's and Children's Health, Uppsala University, 751 85, Uppsala, Sweden.
Xabier Bujanda CundinTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, 80078, Pozzuoli, Italy.ORCID http://orcid.org/0009-0004-4660-7251
Eugenio Del PreteDepartment of Women's and Children's Health, Uppsala University, 751 85, Uppsala, Sweden.ORCID http://orcid.org/0000-0003-3214-9021
Joëlle RüeggDepartment of Organismal Biology, Uppsala University, 752 36, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-6580-9201
Susanne LagerDepartment of Women's and Children's Health, Uppsala University, 751 85, Uppsala, Sweden.ORCID http://orcid.org/0000-0003-3556-065X
Diego di BernardoTelethon Institute of Genetics and Medicine, Via Campi Flegrei 34, 80078, Pozzuoli, Italy.ORCID http://orcid.org/0000-0002-1911-7407
Erika ComascoDepartment of Women's and Children's Health, Science for Life Laboratory, Uppsala University, BMC, POB 593, 75124, Uppsala, Sweden. Erika.comasco@neuro.uu.se.ORCID http://orcid.org/0000-0002-2174-2068
Alkistis SkalkidouDepartment of Women's and Children's Health, Uppsala University, 751 85, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-4935-7532

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripartum depression can have severe impact on the mother's and the infant's health. Yet, its biological underpinnings are largely unknown. The present study sought to identify transcriptomic signatures of depressive symptoms during pregnancy and postpartum. Blood samples were collected during late pregnancy or early postpartum for mRNA isolation and sequencing, while depressive symptoms were assessed using the Edinburgh Postnatal Depression Scale (EPDS). Based on the timepoint when the samples were collected, differentially expressed genes (DEGs) were identified by (1) comparing mRNA levels between the depression symptom trajectory groups, and (2) correlating with EPDS scores. DEGs for samples collected during late pregnancy, but not postpartum, were associated with depressive symptoms occurring only during pregnancy or persisting postpartum, compared with controls. There were 16 upregulated and 109 downregulated DEGs significantly associated with EPDS score at week 32 among samples collected during late pregnancy. Gene Set Enrichment Analysis identified immune response and cell motility as processes linked to these DEGs. Hypothesis-based analysis on previously identified postpartum depressive symptoms-related DEGs replicated a positive association between expression of immune-related genes ISG15 and RSAD2 with postpartum-onset depressive symptoms, both in samples taken during late pregnancy and postpartum. The present findings point to transcriptomic signatures associated with peripartum depressive symptoms, mostly related to immune system dysregulation.

Indexed as

DepressionDepression, PostpartumAdultFemaleGene Expression ProfilingHumansPostpartum PeriodPregnancyPregnancy ComplicationsPsychiatric Status Rating ScalesRNA, MessengerTranscriptomeRNA, Messenger

Identifiers

PMID40473930
PMCPMC12436180

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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.