MicroRNA-148b-3p and MicroRNA-25-3p are overexpressed in fetuses with late-onset fetal growth restriction
Creators
- 1. Servicio de Obstetricia, Hospital Universitario y Politécnico La Fe, Valencia, Spain / Departamento de Pediatría, Obstetricia y Ginecología, Universidad de Valencia, Valencia, Spain
- 2. EpiDisease SL, and Consortium Center for Biomedical Network Research on Rare Diseases (CIBERER). Institute of Health Carlos III. Valencia, Spain / Departamento de Fisiología, Universidad de Valencia, Valencia, Spain
- 3. Servicio de Secuenciación, Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunidad valenciana (FISABIO), Valencia, Spain
- 4. EpiDisease SL, and Consortium Center for Biomedical Network Research on Rare Diseases (CIBERER). Institute of Health Carlos III. Valencia, Spain
- 5. Departamento de Química, Universidad Politécnica de Valencia, Valencia, Spain
- 6. Servicio de Obstetricia, Hospital Universitario y Politécnico La Fe, Valencia, Spain
- 7. Unidad de Bioestadística, Instituto de Investigación Sanitaria La Fe
Description
Objective: to describe a miRNA profile characteristic of late-onset growth restriction (FGR) and to investigate those pathways involved in their biochemical action.
Material and methods: In a prospective study, 25 fetuses: 16 normal and 9 with FGR (estimated fetal weight <10th centile plus cerebroplacental ratio <0,6765 MoM) were evaluated with Doppler ultrasound after 36 weeks. Afterwards, for every fetus, plasma from umbilical vein blood was collected at birth, miRNA was extracted, and full miRNA sequencing was performed. Subsequently, comparisons were done in order to obtain those miRNA that were differentially expressed.
Result: FGR fetuses expressed upregulation of two miRNA: miR-25-3p and especially miR-148b-3p, a miRNA directly involved in Schwann cell migration, neuronal plasticity and energy metabolism (p=0.0072, p=0.0013).
Conclusions: FGR fetuses express a different miRNA profile, which includes overexpression of miR-miR-25-3p and miR-148b-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 miRNAs as a valid tool in the diagnosis and management of FGR.
Notes
Files
Preprint Morales-Rosello Fetal Diagn Ther 2020.pdf
Files
(2.2 MB)
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