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DOI 10.34763/jmotherandchild.20252901.d-25-00019

Медицинская библиотека · Journal of mother and child · 2025

Immune Response and Lipid Metabolism Genes Associated with Acute Cerebral Circulatory Failure in Pre-Eclampsia in a Central Asian Population.

Mirzakhmetova Dinara, Svyatova Gulnara, Berezina Galina, Murtazaliyeva Alexandra

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Аннотация

BACKGROUND

The aim of this study was to determine the association of immune response and lipid metabolism genes with the development of pre-eclampsia and related acute cerebral circulatory disorders in Kazakh women.

MATERIALS AND

METHODS

Minor allele frequencies of immune response and lipid metabolism genes were determined in 1,800 healthy participants stored in the Miras Biobank of the Scientific Centre of Obstetrics, Gynaecology, and Perinatology Joint Stock Company.

RESULTS

The main results of the study showed that TLR4 (rs4986790), PLEKHA1 (rs2281673), PLEKHG1 (rs9478812), APOE (rs7412), FTO (rs1421085) and LPL (rs285) genes were in genetic equilibrium (p > 0.05), indicating that the sample was representative and there were no significant evolutionary pressures on the studied genes. The frequencies of minor alleles in the studied sample of Kazakhs were: TLR4 - 3.3%, PLEKHA1 - 5.9%, PLEKHG1 - 27.0%, APOE - 7.8%, FTO - 28.3% and LPL - 36.0%.

CONCLUSION

The obtained data can be used for further genetic studies, as well as for the development of individualised strategies for the prevention and treatment of pre-eclampsia and related complications. The identified genetic markers may help in early detection of women at increased risk of developing these conditions, which will contribute to improving clinical outcomes and reducing maternal and perinatal mortality.

Для цитирования: Mirzakhmetova Dinara, Svyatova Gulnara, Berezina Galina, Murtazaliyeva Alexandra. Immune Response and Lipid Metabolism Genes Associated with Acute Cerebral Circulatory Failure in Pre-Eclampsia in a Central Asian Population.. Journal of mother and child. 2025. DOI: 10.34763/jmotherandchild.20252901.d-25-00019.

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