Expression analysis of microRNAs and cytokine mRNAs in pregnancies complicated by gestational hypertension

Eur J Obstet Gynecol Reprod Biol. 2024 Oct:301:64-69. doi: 10.1016/j.ejogrb.2024.07.069. Epub 2024 Aug 2.

Abstract

Objectives: Gestational hypertension (GH1) is one of the most common pregnancy-related complications, however, there is still insufficient knowledge about its development and molecular changes. The aim of our study was to examine the expression of miR-17, miR-29a and miR-181a, as well as TNF-α, IL-1β, IL-6 and IL-17 in women with GH and to investigate possible correlations between these parameters.

Study design: The study included 64 pregnant women, placed either in the control or the GH group. Quantitative real-time PCR (qPCR2) was used to determine expression levels of microRNAs and cytokines' mRNAs.

Main outcome measures: Expression levels of miRNAs (miR-17, miR-29a and miR-181a) and proinflammatory cytokines mRNAs (TNF-α, IL-1β, IL-6 and IL-17) in women with gestational hypertension were compared to the control group (healthy pregnant women).

Results: No significant changes in microRNAs expression level were found between compared groups. TNF-α was significantly upregulated in the GH group compared to controls. Expression levels of other investigated cytokines did not differ between examined groups. ROC curve analysis indicated that TNF-α does not show sufficient ability to discriminate between CG and GH patients. TNF-α was significantly positively correlated with IL-1β and IL-17 and negatively correlated with miR-181a.

Conclusions: Our results point to the involvement of proinflamatory cytokines in gestational hypertension. Although increased expression of TNF-α was found in the GH group, this cytokine did not show sufficient ability to discriminate between GH and healthy pregnancies.

Keywords: Biomarker; Gestational hypertension; Proinflamatory cytokine; TNF-α; microRNA.

MeSH terms

  • Adult
  • Case-Control Studies
  • Cytokines* / genetics
  • Female
  • Humans
  • Hypertension, Pregnancy-Induced* / genetics
  • Interleukin-1beta / genetics
  • Interleukin-6 / genetics
  • MicroRNAs* / genetics
  • Pregnancy
  • RNA, Messenger* / metabolism
  • Tumor Necrosis Factor-alpha

Substances

  • MicroRNAs
  • Cytokines
  • RNA, Messenger
  • Tumor Necrosis Factor-alpha
  • Interleukin-1beta
  • MIRN29a microRNA, human
  • MIrn181 microRNA, human
  • Interleukin-6