Abstract

This paper presents molecular genetic research of the TNF- gene polymorphism in pregnant women with fetal loss syndrome. Analysis of molecular genetic research showed that allele A and heterozygous genotypes of the rs1800629 polymorphism in the TNF- gene may be markers of a tendency for an increased risk of developing fetal loss syndrome in Uzbekistan. There is a tendency towards an increase in the frequency of the unfavorable allele A of the TNF- gene in female patients with a severe form of Fetal Loss Syndrome (FLS) as compared with its mild case [1,2].

Highlights

  • The research priority in pathologies in obstetrics and gynecology is studying the state of formation of the ‘mother-placenta-fetus’ functional system, which is the birth of a healthy infant [3,4,5]

  • Among 51 pregnant women, Fetal Loss Syndrome (FLS) was diagnosed in 41 ones, which accounted for 80.4% of cases

  • To assess the clinical course of fetal loss syndrome, we used the working classification used in Fetal Growth Restriction Syndrome (FGRS)

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Summary

Introduction

The research priority in pathologies in obstetrics and gynecology is studying the state of formation of the ‘mother-placenta-fetus’ functional system, which is the birth of a healthy infant [3,4,5]. Studies have demonstrated the role of the proinflammatory cytokine TNF-α in the regulation of apoptosis in the early stages of gestation, its participation in the regulation of the invasion of trophoblast cells is known [7,16,17,18]. This factor enhances the proliferation of T and B cells, the formation of adhesive molecules, acute phase proteins, and activates fibroblasts. TGF-β, isolated from homogenates of placental tissue, is recognized as a topical factor regulating the proliferation and invasion of cytotrophoblast in the placental-uterine region. The study of the distribution of rs1800629 polymorphism in the TNF- gene in fetal loss syndrome is an urgent problem in obstetrics and gynecology

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