Evidence map›Paper›PMID 40918935›Full record

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Differential Expression of Micro-RNA in Maternal Blood of Pregnancies Affected with Late-Onset Fetal Growth Restriction.

José Morales-Roselló, Ana Isabel Martínez-Hernández, Julia Scheel, Gabriela Loscalzo, Eva María García-López, Colin Murdoch

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Article in Biomedicine hub. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited 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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

José Morales-RosellóDepartment of Obstetrics and Gynecology, University and Polytechnical Hospital La Fe, Valencia, Spain.
Ana Isabel Martínez-HernándezDepartment of Obstetrics and Gynecology, Hospital of Manises, Valencia, Spain.
Julia ScheelInstitute for Medical Informatics and Biometry, Faculty of Medicine Carl Gustav Carus, Technique University, Dresden, Germany.
Gabriela LoscalzoDepartment of Obstetrics and Gynecology, University and Polytechnical Hospital La Fe, Valencia, Spain.
Eva María García-LópezEpiDisease SL, and Consortium Center for Biomedical Network Research on Rare Diseases (CIBERER), Institute of Health Carlos III, Valencia, Spain.
Colin MurdochDivision of Cardiovascular Research, School of Medicine, University of Dundee, Dundee, UK.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Micro-RNAs (miRNAs) participate in different biological processes, including fetal hypoxia. In this work, we aimed to evaluate the existence of a miRNA differential expression profile in maternal blood of pregnancies affected with late-onset fetal growth restriction (LO-FGR). Methods: In a prospective study, a group of 35 fetuses were evaluated with Doppler ultrasound after 36 weeks. These included 15 fetuses with LO-FGR defined as fetal birth weight <10th centile plus a cerebroplacental ratio (CPR) <0.6765 MoM and 20 normal fetuses (normal BW plus a normal CPR). Afterward, for every pregnancy, maternal blood plasma was collected at birth, miRNAs were extracted, and full miRNA sequencing was performed using 20 of the indicated samples (12 with LO-FGR and 8 normal), determining the existence of differentially expressed miRNAs. Finally, this differential expression was validated in a wider population of 35 fetuses by means of quantitative reverse transcription polymerase chain reaction. Results: Full mRNA sequencing showed that FGR mothers expressed differential expression of several miRNA. The highest differences were seen for miR-486-5p/3p, miR-516a/b-5p, miR-19a/b-3p, miR-296-5p, miR-10b-5p, miR-205-5p, and Let-7g-5p. However, PCR validation only confirmed significant differences in miR-486-5p/3p. Conclusion: Mothers delivering FGR fetuses express a miRNA profile, which includes differential expression of miR-486-5p/3p. This information might improve our understanding of the pathophysiological processes involved in late-onset FGR. Future validation and feasibility studies will be required to propose maternal blood miRNAs as a valid tool in the diagnosis and management of FGR.

Indexed as

Cardiac modelingDoppler ultrasoundLate-onset fetal growth restrictionLet-7g-5pmiR-486-5p/3p

Identifiers

PMID40918935
PMCPMC12410966

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