GENETIC ASPECTS OF THE IDIOPATHIC RECURRENT MISCARRIAGE.LITERATURE REVIEW
DOI:
https://doi.org/10.34689/bw7v0t48Keywords:
recurrent miscarriage , single nucleotide polymorphism , genotypeAbstract
Introduction. Recurrent miscarriage (hereinafter RM) defined as 2 or more pregnancy losses before the 22nd week of
pregnancy, is a heterogeneous disorder affecting up to 3% of couples in the reproductive period. Despite numerous scientific
studies of the possible causes of RM, their etiology remains uncertain in about 50% of cases and are considered idiopathic
RM (hereinafter iRM), which do not have an explainable etiology. The choice of iRM is the preferred object for genetic
research because of the relevance, clinical and genetic heterogeneity of recurrent miscarriage, the absence of common
diagnostic criteria, the variety of etiological factors determined.
Aim. Conduct a literature review to identify significant genetic variants of the development of iRM.
Research strategy. Search for scientific publications was carried out in search engines: Medline, Web of Science,
PubMed, Cochrane Library Google Academy, elibrary.ru. The depth of the search was not limited. Criteria for inclusion of
publications in the literature review are defined as publications with the full text, in Russian and English, with statistically
verified conclusions. Exclusion criteria are defined as abstracts, newspaper articles. 56 scientific publications were selected
for the study and analysis.
Results. The evidence for the genetic multifactor theory of iRM is growing by eliminating known clinical, ecological and
external environmental risk factors. This review discusses the choice of these particular single nucleotide polymorphisms,
based on a modern understanding of the physiology of implantation processes, which is a long and complex interaction
between the mother and the fetus mediated through the placenta. Violations of this process can lead to abortion at all stages,
which determined our choice of specific polymorphisms of the maternal genome, responsible for impaired endometrial
decidualization and angiogenesis, apoptosis, as well as pro-inflammatory processes.
Conclusions. It's significant contribution to reproduction and fertility indicators due to the high incidence of iRM, it is
necessary to search for possible prognostic clinical biomarkers of iRM for early diagnosis and treatment of the disease.
References
Святова Г.C., Березина Г.М., Салимбаева Д.Н., Кирикбаева М.С., Муртазалиева А.В., Садуакасова К.З.
Генетические аспекты идиопатической формы привычного невынашивания беременности. Обзор литературы //
Наука и здравоохранение. 2019. 4 (Т.21). С. 37-49.
Svyatova G., Berezina G., Salimbayeva D., Kirikbayeva M., Murtazaliyeva A., Saduakasova K. Genetic aspects of the
idiopathic recurrent miscarriage. Literature review. Nauka i Zdravookhranenie [Science & Healthcare]. 2019, (Vol.21) 4, pp. 37-
49.
Святова Г.C., Березина Г.М., Салимбаева Д.Н., Кирикбаева М.С., Муртазалиева А.В., Садуакасова К.З.
Үйреншікті үктілікті көтермеудің идиопатиялық түрінің генетикалы қаспектілері. Әдебиетке шолу // Ғылым және
Денсаулық сақтау. 2019. 4 (Т.21). Б. 37-49.
Downloads
Published
License
Copyright (c) 2026 Гульнара Святова, Галина Березина, Дамиля Салимбаева, Меруерт Кирикбаева, Александра Муртазалиева, Корлан Садуакасова (Автор)

This work is licensed under a Creative Commons Attribution 4.0 International License.