Evidence map›Paper›PMID 40013652›Full record

ArticleThe Journal of physiology2025

MicroRNA profiling in umbilical cord plasma: links to maternal metabolism and neonatal metabolic and inflammatory traits.

Jasmin Zaunschirm-Strutz, Anna Rieder, Carolina Tocantins, Mariana S Diniz, Elisa Weiss, Ursula Hiden

Abstract read
In one paragraph

Article in The Journal of physiology, 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. Article
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

6 authors.

Jasmin Zaunschirm-StrutzDepartment of Obstetrics and Gynecology, Research Unit Early Life Determinants (ELiD), Medical University of Graz, Graz, Austria.ORCID 0000-0002-6138-7566
Anna RiederInstitute of Biomedical Sciences, Carinthian University of Applied Science, Klagenfurt, Austria.
Carolina TocantinsDepartment of Obstetrics and Gynecology, Research Unit Early Life Determinants (ELiD), Medical University of Graz, Graz, Austria.ORCID 0000-0002-3758-0454
Mariana S DinizDepartment of Obstetrics and Gynecology, Research Unit Early Life Determinants (ELiD), Medical University of Graz, Graz, Austria.ORCID 0000-0002-2161-9676
Elisa WeissDepartment of Obstetrics and Gynecology, Research Unit Early Life Determinants (ELiD), Medical University of Graz, Graz, Austria.ORCID 0000-0002-0958-8280
Ursula HidenDepartment of Obstetrics and Gynecology, Research Unit Early Life Determinants (ELiD), Medical University of Graz, Graz, Austria.ORCID 0000-0001-8009-020X

Funding

Austrian Science Fund (FWF) 10.55776/KLI1023Carinthia University of Applied Sciences (CUAS) PJ02
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are regulators of mRNA translation and play crucial roles in various physiological and pathological processes. In this study, we profiled miRNAs in umbilical cord plasma (UCP) to explore the association of neonatal circulating miRNAs with maternal metabolic parameters and neonatal anthropometric, metabolic and inflammatory characteristics in healthy pregnancies. Data and UCP samples were collected from 16 pregnancies, equally divided between normal-weight and overweight mothers and between male and female newborns. Using next-generation sequencing, we identified and quantified miRNAs in UCP, alongside the analysis of metabolic and inflammatory parameters. Our results revealed that the majority of UCP miRNAs are sensitive to maternal and neonatal characteristics, particularly maternal body mass index, gestational weight gain, placental weight, UCP leptin, UCP C-reactive protein and UCP insulin levels. Notably, we identified a strong association between the placenta-derived chromosome 19 microRNA cluster (C19MC) and placental weight, gestational weight gain, UCP insulin and neonatal weight. Likewise, the pregnancy-specific chromosome 14 microRNA cluster (C14MC) was associated with maternal body mass index and UCP leptin. Our study highlights the sensitivity of UCP miRNAs to maternal metabolic conditions, demonstrates their association with neonatal metabolic and inflammatory traits, and underscores the potential role of circulating cord blood miRNAs in fetal metabolism and development. KEY POINTS: MicroRNAs (miRNAs) are regulatory RNA molecules that modulate protein expression. They are present in all body fluids and umbilical cord plasma and are affected by metabolic changes. Pregnancy is a state of metabolic change in the mother, and maternal metabolism affects fetal development. We found that the composition of umbilical cord blood miRNAs is associated with maternal and neonatal metabolism. Pregnancy-specific groups of miRNAs showed particular patterns, with miRNAs encoded by a region of chromosome 14 associated with maternal body mass index and with miRNAs encoded by a specific region of chromosome 19 associated with umbilical cord plasma insulin. MicroRNAs represent a separate dimension through which maternal metabolism can influence fetal development.

Indexed as

Circulating MicroRNAMaternal HealthPregnancyAdultBody Mass IndexCluster AnalysisFemaleFetal BloodGene Expression ProfilingGestational Weight GainHumansInfant, NewbornInflammationMaleMetabolismPlacentaCirculating MicroRNAcirculating microRNAsmaternal body mass indexneonatal homeostatic model assessment of insulin resistanceplacental weightumbilical cord plasma

Identifiers

PMID40013652
PMCPMC11908477

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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.