Journal of obstetrics and women's diseases
Peer-review bimonthly medical journal
Editor-in-Chief
Eduard K. Ailamazyan, MD, PhD, Academician of the Russian Academy of Sciences
Publisher
- Eco-Vector
WEB: https://eco-vector.com/
About
The Journal has been issued since 1887. It is the first scientific journal in Russia for obstetricians and gynecologists. For over a century, the Journal regularly covers the latest achievements of Russian science.
Journal of Obstetrics and Women's Diseases, a Gold Open Access journal, publishes six volumes per year. Additionally, the Journal will publish occasional special issues featuring selected papers from major conferences.
Journal Topics
Journal of Obstetrics and Women's Diseases is a scientific and practical peer-reviewed medical journal, which discusses the most pressing health issues:
- reproductive health;
- results of clinical and sociological research;
- current problems in perinatal obstetrics;
- issues of gynecological endocrinology, pregravid preparation, and family planning;
- actual problems in operative gynecology;
- diagnostics and therapy of reproductive tract infections;
- advances in clinical genetics and prenatal diagnosis of hereditary and congenital diseases, immunology, and pathology;
- new and important information and recommendations for the practical physicians (introduction of modern diagnostic and therapeutic technologies, the use of effective drugs, etc.);
- impact of harmful environmental and production factors on the female reproductive system.
Journal Mission
The main mission of the Journal is to provide new scientific and technical information, to promote scientific knowledge, to help obstetricians and gynecologists to choose the best methods of diagnosis and treatment, and to help improve their skills.
The publications of the Journal are of interest to a wide range of scholars in the field of obstetrics, gynecology, reproduction, genetics, pathology, and immunology of reproduction, as well as for medicine and biology tutors and students.
Abstracting and Indexing
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- Google Scholar
- Scilit
- SCOPUS
- EmBase
- Ulrich's Periodicals Directory
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Announcements More Announcements...
III Congress with international participation “Aesthetic Gynecology and Anti-Aging Medicine”, 2026 March 4-6, MoscowPosted: 20.02.2026
Dear colleagues and readers! |
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Current Issue
Vol 74, No 6 (2025)
- Year: 2025
- Published: 04.03.2026
- Articles: 13
- URL: https://journals.eco-vector.com/jowd/issue/view/14077
- DOI: https://doi.org/10.17816/JOWD.746
Original study articles
Assessment of fetal fractional limb volume for predicting neonatal body composition and hypoglycemia: a cohort study
Abstract
BACKGROUND: Neonates with excessive body fat deposition are at increased risk of adverse short- and long-term outcomes. The potential of fractional fetal thigh (TVol) and arm (AVol) volume assessment to predict fetal body composition at birth, including but not limited to neonates of mothers with diabetes mellitus, is to be investigated.
AIM: The aim of this study was to investigate the association between the extended fetal biometry measurements, based on the calculation of fetal fractional limb volumes, the neonatal body composition, and the development of neonatal hypoglycemia.
METHODS: This single-center cohort study included patients with singleton pregnancies divided into the study groups: pregestational diabetes mellitus, gestational diabetes mellitus, and no carbohydrate metabolism disorders. Routine fetal biometry and TVol and AVol assessment were performed within 7 days before delivery. Body fat mass at birth was calculated using the Catalano et al. (1995) equation.
RESULTS: The study included 46 patients with diabetes mellitus (pregestational, n = 32; gestational, n = 14) and 18 healthy control individuals, as well as their children. In newborns with diabetic fetopathy, the percentage of body fat was the highest — 25.0 [22.1; 26.1]% (p < 0.001). Neonates in the pregestational diabetes mellitus group had a higher weight-for-length Z-score (INTERGROWTH-21st) — 1.253 [0.663; 2.058] (p = 0.001), in the gestational diabetes mellitus group — 0.247 [0.014; 0.411] (p = 0.001), and in the control group — 0.485 [0.059; 0.887] (p = 0.004). The percentage of body fat mass was strongly associated (p < 0.001) with neonatal weight (r = 0.706) and its Z-score (r = 0.840), the weight-for-length ratio and its Z-score (r = 0.843), TVol (r = 0.639), and AVol (r = 0.532). The percentage of body fat mass did not correlate with the estimated fetal weight (r = 0.135, p = 0.288). A linear regression model including TVol and gestational age at birth had r2 = 0.64 (p < 0.001) for body fat mass prediction. Generalized linear models identified pregestational diabetes mellitus as independent risk factor (p < 0.001) for higher body fat mass percentage with comparable TVol. For neonatal hypoglycemia prediction, the birth weight Z-score (sensitivity 66.7%, specificity 70.0%) and the weight-for-length Z-score (sensitivity 66.7%, specificity 75.0%) were unreliable estimates, whereas the percentage of body fat mass had better performance (sensitivity 70.8%, specificity 80.0% at a percentage of greater than or equal to 20.2%).
CONCLUSION: The accuracy of fetal adiposity detection and assessing the risk of neonatal hypoglycemia can be improved by using fetal fractional limb volume measurements. TVol is a sonographic predictor for excessive fat deposition, which can be used for body fat mass calculation, while parameters measured during routine fetometry poorly reflect the distribution of fat tissue in the fetus.
5-18
The role of the AGER gene in different phenotypes of polycystic ovary syndrome
Abstract
BACKGROUND: Polycystic ovary syndrome is the most common endocrine disorder in women of reproductive age. It increases the risk of infertility, metabolic disorders (including type 2 diabetes mellitus), cardiovascular diseases, endometrial hyperplasia, and psychological disorders. Hyperglycemia is a leading metabolic factor that results in the development of vascular complications of diabetes mellitus. The pathogenesis of the damaging effect of hyperglycemia is associated with the accumulation of early and advanced glycation end products in tissues, which are non-enzymatic glycation and protein oxidation products. The receptor for advanced glycation end products (RAGE) is a transmembrane multiligand cell surface receptor encoded by the AGER gene, which produces multiple transcripts. It is expressed primarily in the lungs and is involved in initiating and sustaining an adverse proinflammatory state. Due to its diverse functions, AGER is implicated in the development of many diseases, particularly diabetes mellitus and cardiovascular diseases. However, there is no literature on the association between AGER gene polymorphisms and polycystic ovary syndrome.
AIM: The aim of this study was to assess the frequency of rs2070600 and rs2071288 single-nucleotide variants in the AGER gene in different polycystic ovary syndrome phenotypes, and to determine the presence of an association between the gene polymorphism and lipoprotein levels in the blood serum.
METHODS: This single-center cohort study involved patients with polycystic ovary syndrome representing various phenotypes. The patients were divided into two large groups based on the presence or absence of carbohydrate metabolism disorders. Blood samples were collected for genotyping, which was performed using polymerase chain reaction followed by restriction fragment length polymorphism analysis. Statistical data processing was used to calculate the frequency of single nucleotide variants in the AGER gene.
RESULTS: 93 patients were included: 42 (45.2%) women with the classical phenotype (A), 20 (21.5%) with the anovulatory phenotype (B), 17 (18.3%) with the ovulatory phenotype (C), and 14 (15.0%) with the non-androgenic phenotype (D). The main group comprised patients without carbohydrate metabolism disorders (n = 19), while the comparison group consisted of patients with various types of such disorders (n = 74). The heterozygous G/A genotype of the AGER gene rs2070600 variant was found in patients with different polycystic ovary syndrome phenotypes in combination with carbohydrate metabolism disorders. In contrast, this genotype was not detected in patients with polycystic ovary syndrome without carbohydrate metabolism disorders. The heterozygous G/A genotype of the AGER gene rs2070600 variant was most frequently identified in patients with polycystic ovary syndrome phenotype D (non-androgenic, 14% of cases) and phenotype A (classical, 9.5% of cases). Patients with heterozygous G/A genotype had a higher serum level of low-density lipoproteins compared to those with the homozygous G/G genotype (3.2 ± 0.83 vs. 2.73 ± 0.76 mmol/L; p < 0.001).
CONCLUSION: The data obtained suggest that the heterozygous G/A genotype of the AGER gene rs2070600 variant may be associated with various carbohydrate metabolism disorders in patients with polycystic ovary syndrome and may contribute negatively to the development of cardiovascular diseases, taking into account the relationship of the genotype with low-density lipoprotein cholesterol level.
19-29
The efficiency of complex endothelioprotective therapy in women with chronic salpingo-oophoritis and diminished ovarian reserve
Abstract
BACKGROUND: The relevance of studying the pathological mechanisms that lead to reduction of ovarian reserve is due to the growing problem of female infertility. This is largely related to the disruption of ovarian function. Chronic salpingo-oophoritis is a significant factor in this disorder. Oxidative stress and impaired vascular endothelial function, coupled with chronic inflammation, lead to deterioration of microcirculation in ovarian tissue and contribute to a decrease in folliculogenesis. The development of new approaches to the prevention and treatment of ovarian dysfunction can significantly improve the reproductive capacity of women with chronic salpingo-oophoritis.
AIM: The aim of this study was to evaluate the function of the vascular endothelium and blood flow parameters in the ovaries in women with chronic salpingo-oophoritis and diminished ovarian reserve during complex treatment using preformed factors.
METHODS: This non-randomized, controlled clinical trial was conducted to evaluate ovarian reserve, ovarian artery blood flow, and vascular endothelial function markers in women with diminished ovarian reserve and chronic salpingo-oophoritis during their prime reproductive years. These patients were divided into two study groups (a main group and a comparison group). Both groups received dydrogesterone 20 mg/day orally during the second phase of the menstrual cycle. In the main group, vaginal laser and magnetic therapy was additionally performed during the first phase of the menstrual cycle. The parameters studied were evaluated before and after treatment and were compared with those in a control group of otherwise healthy women.
RESULTS: Patients with chronic salpingo-oophoritis and diminished ovarian reserve (n = 70) in the main group (n = 42) and comparison group (n = 28) showed hemodynamic changes in the ovarian arteries, as well as deterioration of ovarian hormonal function and folliculogenesis, which was accompanied by changes in the condition and function of the vascular endothelium. The control group included 22 women. The application of preformed factors in the treatment improved ovarian blood flow, restored vascular endothelial function, and, consequently, enhanced follicle recruitment and increased ovarian reserve in the selected contingent of patients.
CONCLUSION: The use of preformed factors opens up new treatment options for women with chronic salpingo-oophoritis and diminished ovarian reserve. This allows for improving the prognosis for reproductive restoration and increasing the chances of successful conception.
30-37
Differentiated evaluation of intravenous immunoglobulins in patients with recurrent implantation failure in assisted reproductive technology
Abstract
BACKGROUND: Currently, the use of intravenous immunoglobulins in patients with recurrent implantation failure after in vitro fertilization is controversial due to the lack of standard treatment protocols and the heterogeneity of patient selection criteria for this therapy. This study was the first to compare the outcomes of assisted reproductive technology cycles using intravenous immunoglobulin therapy in patients with immunological factors for reproductive failure and chronic endometritis.
AIM: The aim of this study was to develop a differentiated approach to the use of intravenous immunoglobulins in patients with recurrent implantation failure in assisted reproductive technology cycles.
METHODS: This cohort study included patients with various causes of infertility and at least one unsuccessful embryo transfer who were treated between 2024 and 2025. All patients received immunomodulatory therapy using intravenous immunoglobulins at a dose of 15 g per course. Patients were stratified by the presence of antiphospholipid antibodies and chronic endometritis. The final analysis of the effectiveness of the assisted reproductive technology program included patients with optimal quality embryo transfers.
RESULTS: The study included 131 patients. The presence of antiphospholipid antibodies was associated with a higher efficiency of transfer of frozen embryos of optimal quality compared to patients with chronic endometritis (76.0% versus 48.4%, respectively; p = 0.035), which indicates different sensitivity of these clinical phenotypes to intravenous immunoglobulins therapy.
CONCLUSION: Immunotherapy with intravenous immunoglobulins is effective as part of combination therapy for patients with immune-related forms of reproductive disorders, particularly in the presence of antiphospholipid antibodies. In chronic endometritis, the efficacy of intravenous immunoglobulins is limited. Further research is needed to optimize their regimens and conditions. Diagnosis and treatment of chronic endometritis are essential before entering assisted reproductive technology programs.
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Clinical features of endometriosis in patients with type 1 diabetes mellitus
Abstract
BACKGROUND: Endometriosis affects 5–10% of women of reproductive age worldwide. Despite the high prevalence of the disease, its diagnosis is usually delayed for several years and misdiagnosis is common, leading to delay in effective pathogen-based treatment. Early diagnosis and timely treatment of endometriosis are particularly important in patients with type 1 diabetes mellitus, as the longer the disease lasts, the greater the risk of vascular complications and the lower ovarian reserve, thus decreasing the reproductive capacity.
AIM: The aim of this study was to analyze the clinical features of endometriosis in patients with type 1 diabetes mellitus allowing for a timely and accurate diagnosis.
METHODS: This clinical study included women with endometriosis, type 1 diabetes mellitus, and a combination of the two. The control group consisted of healthy women of reproductive age. The diagnosis of endometriosis was confirmed by laparoscopic surgery and verified by histological examination. Serum anti-Müllerian hormone levels were determined using the immunochemiluminescence method from days 2 to 5 of the menstrual cycle. Glycated hemoglobin levels were measured in patients with type 1 diabetes mellitus.
RESULTS: The study included 51 patients with endometriosis, 209 patients with type 1 diabetes mellitus, 79 patients with a combination of these diseases, and 31 conditionally healthy women. In patients with endometriosis combined with type 1 diabetes mellitus, the frequency of abnormal uterine bleeding was 31%, which is higher than in patients with only type 1 diabetes mellitus (11%), but lower than in those with only endometriosis (71%). Dysmenorrhea according to the McGill visual analogue pain scale in patients with endometriosis combined with type 1 diabetes mellitus was 3.9 ± 1.48 points, with endometriosis 7.06 ± 1.27 points, and with type 1 diabetes mellitus 1.2 ± 0.7 points. In patients with endometriosis combined with type 1 diabetes mellitus, there was a decrease in the number of antral follicles (8 ± 3) and anti-Müllerian hormone level (3.12 ± 1.78 ng/ml) compared to patients with type 1 diabetes mellitus (12 ± 4, 3.52 ± 2.0 ng/ml, respectively). The most pronounced decrease in the number of antral follicles (4 ± 2) and anti-Müllerian hormone level (0.94 ± 0.4 ng/ml) was found in patients with endometriosis. The incidence of deep infiltrative endometriosis was higher in patients without diabetes mellitus, occurring in 71% of cases. In patients with endometriosis combined with type 1 diabetes mellitus, it only occurred in 42% of cases. Endometrioid cysts were found in 42% of patients without type 1 diabetes mellitus and in 22% of those with the disease. Repeat surgical interventions were performed in 25% of patients with endometriosis without type 1 diabetes mellitus, compared to only 10% of women with endometriosis combined with type 1 diabetes mellitus.
CONCLUSION: Late diagnosis and delayed treatment of endometriosis, which is often asymptomatic when combined with type 1 diabetes mellitus, can lead to a decrease in ovarian reserve and infertility. In patients with type 1 diabetes mellitus, endometriosis should be suspected in the presence of mild pain, abnormal uterine bleeding, decreased anti-Müllerian hormone levels and antral follicle count, and infertility to ensure timely diagnosis and selection of treatment strategies. Diabetic patients require a long period of pre-pregnancy planning in order to compensate for their disease.
50-60
Oxytocin receptor gene expression in patients with uterine fibroids
Abstract
BACKGROUND: Uterine fibroids are hormone-dependent tumors in which the local microenvironment and the fibroid pseudocapsule play an important role. The oxytocin receptor, encoded by the OTR gene, may contribute to the regulation of contractile activity, vascularization, and tissue remodeling; however, its expression in the pseudocapsule remains insufficiently studied.
AIM: The aim of this study was to assess oxytocin receptor expression in fibroid nodules, the pseudocapsule, and intact myometrium in women with uterine fibroids.
METHODS: This single-center case series included patients of reproductive-age with isolated uterine fibroids who underwent laparoscopic myomectomy. OTR mRNA expression in the dominant fibroid, its pseudocapsule, and the myometrium was determined using real-time polymerase chain reaction. The nodules were typed based on the presence of a somatic MED12 gene mutation and HMGA2 gene overexpression. Statistical analysis was performed using nonparametric tests (p < 0.05).
RESULTS: The study included 27 patients. OTR gene expression was increased in the myometrium and pseudocapsule compared to the fibroid nodules. In all examined nodules, the OTR gene was expressed at a low level or was not detected. No association was found between fibroid size and OTR gene expression in either the myometrium or the pseudocapsule. Comparison of patients with a solitary fibroid versus multiple fibroids revealed no differences in OTR gene expression. Myometrial OTR gene overexpression was characteristic of fibroid nodules harboring a MED12 gene mutation, whereas in the absence of such mutations, OTR gene expression in the myometrium remained low or undetectable. In nodules with HMGA2 gene overexpression, OTR mRNA levels in the myometrium also remained low. No differences in the pseudocapsule OTR gene expression were found between patient subgroups with different driver types. In the pseudocapsule, OTR gene expression levels were higher in the luteal phase than in the follicular phase of the menstrual cycle.
CONCLUSION: The pseudocapsule and adjacent myometrium in patients with uterine fibroids are characterized by overexpression of the OTR gene, while OTR gene expression remains low in the fibroid tissue. The identified associations between OTR gene expression levels and MED12 status confirm a compartment-specific impact of driver genetic events on the oxytocin system. Increased OTR gene expression in the pseudocapsule indicates its specific hormonal sensitivity and supports the concept of the pseudocapsule as an independent structural and functional unit that may contribute to the regulation of growth, vascularization, and repair in uterine fibroids.
61-70
Factors influencing participation of reproductive-age patients in preconceptional screening: analysis of sociological survey data
Abstract
BACKGROUND: Hereditary monogenic diseases are a significant medical and social problem that burdens the healthcare system and affects thousands of families worldwide. Preconception screening is a key element in the primary prevention of these pathologies. Despite its proven clinical significance, public awareness about the benefits of pre-pregnancy training, including preconception screening, remains unsatisfactory. According to the World Health Organization data (2023), only 30–40% of couples planning a pregnancy undergo a comprehensive examination before conception.
AIM: The aim of this study was to assess patients’ knowledge about preconception screening options.
METHODS: This cross-sectional comprehensive study was conducted in the field of sociology of medicine, in which patients from St. Petersburg, Russia participated on a voluntary and anonymous basis. We developed a 24-question survey questionnaire that was administered online using a Google Form.
RESULTS: The study involved 209 respondents of different age groups. The questionnaire was asked to be filled out by both individual female patients at the reception and couples who attended the appointment together. The main factors contributing to the low appeal of women of reproductive age regarding preconception screening are a lack of awareness of the benefits of this type of pre-pregnancy training, the perception of preconception screening as an unnecessarily expensive diagnostic procedure, and organizational barriers, including the lack of specialized programs at the primary healthcare level.
CONCLUSION: To expand preconception screening coverage, it is advisable to raise patient awareness, train specialists in this field, and develop clinical guidelines, examination protocols, and algorithms for managing identified risk factors. The implementation of these measures will reduce the incidence of pregnancy complications, improve newborn health outcomes, and optimize healthcare costs. Further research should be aimed at evaluating the effectiveness of various preconception counseling models, depending on regional characteristics and sociodemographic groups.
71-82
Features of spinal anesthesia for cesarean section in patients with different types of diabetes mellitus: a controlled non-randomized study
Abstract
BACKGROUND: Despite national reports on diabetes mellitus in pregnancy, the impact of different types of the disease on the features of anesthesia and the postoperative period in patients has not been studied well enough.
AIM: The aim of this study was to evaluate the features of anesthesia during abdominal cesarean section and the postoperative period in patients with different types of diabetes mellitus.
METHODS: We conducted a non-randomized controlled clinical study to examine the details of anesthetic management for cesarean section in patients with various types of diabetes mellitus. The patients underwent cesarean section under spinal anesthesia (10–12.5 mg of hyperbaric bupivacaine) using standard techniques. We studied the development and regression of motor block, as measured by the Bromage scale, and the progression of sensory block to the Th4–Th5 level.
RESULTS: The study included 190 patients. Pregestational and gestational metabolic disorders contributed to a slowing of the blockade of sensorimotor fibers of the spinal nerves after spinal anesthesia with 0.5% hyperbaric bupivacaine. In all groups of patients with diabetes mellitus, the development of motor block to Bromage score 3 and sensory block to the Th4–Th5 level differed from the control group (p < 0.001), but did not differ between groups with different types of glycemic disorders. The rate of regression of sensorimotor block in the study groups differed from rate of its development. In patients with type 1 or type 2 diabetes mellitus, regression of both sensory and motor blocks was longer by an average of 20 minutes (134.0–140.0 [128; 140] and 184.0–188.0 [180; 190] minutes, respectively) compared to healthy parturients. In patients with gestational diabetes mellitus, we observed the opposite reaction, namely, regression of sensory and motor blocks occurred on average 10 minutes faster (110.0–112.0 [110; 114] and 155.0 [150; 160] minutes, respectively) than in patients of the control group (121.0 [115; 128] and 165.0 [160; 170] minutes, respectively).
CONCLUSION: Spinal anesthesia, as the preferred anesthetic option for cesarean section, has its own unique challenges for women with pregestational and gestational diabetes. However, the longer time to achieve sensory and motor block in these patients should be taken into account when choosing an anesthesia method based on abdominal delivery urgency.
83-94
Potential applications of vocal three-dimensional angiography in assessing cervical vascularization during pregnancy
Abstract
BACKGROUND: VOCAL (Virtual Organ Computer-aided AnaLysis) software enables quantitative assessment of vascularization in anatomical structures based on three-dimensional reconstruction combined with power Doppler imaging. Available scientific databases, including PubMed and Google Scholar, lack systematized studies focused on the dynamic analysis of regional cervical vascularization throughout gestation using VOCAL technology.
AIM: The aim of this study was to evaluate cervical vascularization using three-dimensional power Doppler angiography using VOCAL at different gestational stages.
METHODS: This single-center cohort study included women with singleton pregnancies at 7+0–41+0 weeks of gestation. The VOCAL analytical subsample included cases with a complete data set. The protocol comprised transvaginal cervicometry, elastography (using E-Cervix parameters such as hardness ratio, elasticity contrast index, internal os strain, external os strain, and cervical length), and three-dimensional power Doppler angiography of the cervix with automatic calculation of the vascularization index, flow index, and vascularization flow index.
RESULTS: We performed 516 ultrasound examinations in 337 pregnant women. The VOCAL analytical subsample included cases with a complete data set (n = 223). Cluster analysis identified three distinct cervical phenotypes: immature, ripening, and mature. The vascular indices (vascularization index, flow index, vascularization flow index) increased progressively from the immature phenotype to the mature phenotype. The association of vascular indices with gestational age was moderately positive (Spearman’s rank correlation coefficient ρ ranged from 0.324 to 0.359; p < 0.001), whereas that with cervical length was weakly negative (ρ ranged from −0.161 to −0.224). In the full-term pregnancy subgroup, the vascularization index showed the highest diagnostic performance for identifying a mature cervix (phenotype 3) with an AUC of 0.729.
CONCLUSION: Three-dimensional power Doppler angiography using VOCAL is a method for assessing cervical vascularization during pregnancy. Increased cervical vascularization is associated with elastographic signs of cervical maturation and increased gestational age, but is weakly related to cervical shortening, which limits the prognostic value of isolated cervicometry. A comprehensive ultrasound assessment using elastography and vascular indices may serve as a useful tool for identifying physiological and premature cervical remodeling.
95-104
Local synthesis of neuropeptides in female reproductive tissues and synergism of kisspeptin and oxytocin in endometriosis development
Abstract
BACKGROUND: Previous studies leave no doubt as to the involvement of kisspeptin and oxytocin in the pathogenesis of endometriosis. Oxytocin and kisspeptin levels in the peripheral blood of patients with endometriosis were shown to be higher than in the comparison group, and these proteins were detected in the eutopic endometrium of patients with endometriosis. Local synthesis of these neuropeptides in female reproductive tissues may presumably play a significant role in the development of the disease.
AIM: The aim of this study was to evaluate KISS1 and OXT gene expressions in the peritoneum, ectopic and eutopic endometrium of patients with endometriosis and women in the comparison group.
METHODS: This single-center cohort study analyzed a collection of tissues (eutopic endometrium, peritoneum, peritoneal endometrioid heterotopias, endometrioid ovarian cysts, endometrioid infiltrates) obtained from patients with endometriosis and a comparison group of women undergoing examination and treatment at the Research Institute of Obstetrics, Gynecology and Reproductology named after D.O. Ott. Total RNA was isolated from the samples, and the relative expression levels of the KISS1 and OXT genes were determined using real-time reverse transcription-polymerase chain reaction.
RESULTS: The main group included 106 patients, and the comparison group included 104 individuals. The following gene expression patterns were found in patients with endometriosis. KISS1 gene overexpression was detected in the peritoneum and, to a lesser extent, in the eutopic endometrium. OXT gene expression was elevated in the eutopic endometrium and, in some cases, in the peritoneum. OXT gene overexpression was observed in endometriotic infiltrates, but not in peritoneal lesions or endometriotic cysts.
CONCLUSION: In endometriosis, the KISS1 and OXT genes are expressed at high levels in peripheral tissues (endometrium, peritoneum). These expression patterns are tissue-specific and are observed not only in endometriotic lesions (endometrioid infiltrates) but also in morphologically normal tissues. Possible mechanisms by which kisspeptin and oxytocin influence the development of the symptom complex of endometriosis are discussed.
105-114
Reviews
Modern concepts of pathogenesis, predictors of development and prevention of preeclampsia
Abstract
Preeclampsia is one of the most common complications of the second half of pregnancy, which poses a threat to the life and health of both the mother and the fetus. The problem remains relevant to this day, due to the lack of a clear understanding of the pathogenesis of the disease, because of which there is no unified classification, early diagnostic methods, or effective treatment. According to the World Health Organization, conditions associated with hypertension are among the leaders in the structure of maternal mortality worldwide. According to Rosstat, this pregnancy complication ranks fourth. Preeclampsia not only affects the health of the woman, but also leads to disorders in the fetus such as an increased risk of perinatal mortality, growth retardation, and chronic hypoxia. Children from mothers with hypertensive disorders are susceptible to delayed development of nervous, cardiovascular, and endocrine diseases.
According to the clinical guidelines from the Russian Society of Obstetricians and Gynecologists and the American Society of Obstetricians and Gynecologists, this complication is a hypertensive disorder combined with proteinuria and signs of other failing organs or systems and developing from 20 weeks of pregnancy. Currently, preeclampsia is classified depending on the gestational age at diagnosis or at delivery: early (up to 34 weeks) and late (after 34 weeks). This distinction is based on different pathogenesis, severity of symptoms, and different perinatal outcomes.
To effectively reduce the incidence of preeclampsia and associated complications, it is necessary to base the work algorithm on early detection and risk stratification, taking into account the presence of aspirin resistance in a certain proportion of pregnant women.
115-121
Hormonal regulation of labor: a review of physiological mechanisms and diagnostic capabilities
Abstract
Labor is a complex biological process triggered by the coordinated interaction of multiple hormonal signals that regulate the transition of the myometrium from a resting state to an active contractile phase. The purpose of this review article was to systematize current data on the roles of progesterone, oxytocin, cortisol, and prostaglandins in initiating labor, as well as to analyze their levels in various biological media such as blood, urine, amniotic fluid, and cervical mucus.
The article details the mechanisms of action of each hormone at the level of receptor interactions, second messengers, and tissue specificity. The discussion covers the concepts of functional progesterone withdrawal, isoform regulation of progesterone receptors, oxytocin receptor expression in the myometrium and amnion, the role of glucocorticoids in inducing steroid switching, as well as paracrine and autocrine effects of prostaglandins.
Special attention is given to the potential use of changes in the levels of these hormones in bodily fluids as biomarkers for predicting the onset of labor and assessing the risk of uterine contraction abnormalities. The presented data emphasize the promise of comprehensive hormonal monitoring as a tool for personalized obstetric care.
Current research demonstrates that hormonal dynamics are strictly individual and depend on multiple factors such as gestational age, the mother’s somatic status, the presence of comorbidities, and even genetic characteristics. In particular, women with preeclampsia or fetal growth restriction show marked deviations in progesterone and cortisol profiles. This opens up prospects for developing prognostic algorithms that take into account not only absolute hormone values but also their ratios in various biological fluids.
Furthermore, the introduction of highly sensitive analytical methods (such as mass spectrometry and enzyme-linked immunosorbent assay) enables the detection of subtle concentration fluctuations even among low-abundance metabolites. Such data could serve as the foundation for developing diagnostic panels capable of providing early warning signs of the risk of preterm labor or uterine inertia. In the long term, this will enable a shift from reactive to preventive pregnancy management, significantly reducing the incidence of obstetric complications.
122-134
Case reports
Fertility preservation in a patient with stage 1 multiple primary endometrial and ovarian cancer during hormonal therapy using a levonorgestrel-releasing intrauterine system
Abstract
Preserving the fertility of patients with multiple primary gynecological malignancies is a pressing issue in reproductive medicine. Organ-preserving treatment, combined with assisted reproductive technology, enables these patients to achieve their reproductive plans.
From August 2022 to May 2025, assisted reproductive technology programs were conducted to preserve fertility in a cancer patient with synchronous malignant neoplasm of the endometrium stage TIA1 and ovary stage T1a without signs of stromal invasion in a borderline endometrial tumor.
The patient underwent successful primary organ-preserving treatment in 2018 and repeat treatment in 2020 for recurrent endometrial cancer. Given the absence of disease progression over two years, the patient entered a program of assisted reproductive technology to preserve fertility. From August 2022 to May 2025, she underwent 14 transvaginal follicle punctures in a natural cycle, followed by vitrification of 13 stage MII oocytes using a levonorgestrel-releasing intrauterine system. In 3 cases, oocytes were retrieved from the right ovary, in 10 cases from the left ovary, and in 1 case, no oocyte was retrieved from the left ovary.
The patient was observed and examined every 3 months, while using a levonorgestrel-releasing intrauterine system. No signs of recurrence of ovarian cancer or endometrial cancer were detected.
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