Акушерство, гинекология и репродукция (Jul 2023)

Expression profile of plasma microRNAs and target genes in patients with complicated pregnancy

  • M. D. Umerova,
  • S. S. Alyadinova,
  • M. J. Khonjonova,
  • R. A. Balakadasheva,
  • E. E. Menadzhiev,
  • D. I. Kharchuk,
  • D. O. Leus,
  • G. I. Islyamova,
  • M. I. Islyamova,
  • S. L. Abkarimova,
  • D. S. Kasabyan,
  • L. E. Sorokina

DOI
https://doi.org/10.17749/2313-7347/ob.gyn.rep.2023.420
Journal volume & issue
Vol. 17, no. 3
pp. 309 – 320

Abstract

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Aim: to assess features of placental transcriptome in patients with complicated pregnancy course and outcome.Materials and Methods. A prospective observational comparative study in parallel groups was carried out by examining 44 patients divided into three groups: group 1 included 13 pregnant women with moderate and severe preeclampsia (PE), group 2 consisted of 12 patients with fetal growth retardation (FGR), control group included 19 clinically healthy women with uncomplicated pregnancy and delivery. All women enrolled to the study underwent a comprehensive examination, including history collection, general and obstetric-gynecological examination, laboratory and instrumental studies. Special research methods were used during the study, which included placental tissue sampling followed by analyzed expression profile of 12 microRNAs using real-time polymerase chain reaction (PCR).Results. The PCR data indicated about lack of expression for analyzed miR-210-3p, miR-320-3p, miR-1304-5p and miR-375-5p in placental tissue samples in FGR patients. No significant differences in placental miRNA levels were observed in FGR vs. PE and control group. Analysis of placenta-specific microRNAs in women with PE vs. control group showed a significantly down modulated expression level for miR-517a-3p (p = 0.025), miR-517c-3p (p = 0.036), miR-574-5p (p = 0.015) along with upregulated expression of miR-20a-5p (p = 0.046).Conclusion. The data obtained evidence that pregnancy-related complications are characterized by specific molecular changes at placental transcriptome level.

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