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

**Authors:** Dinara Mirzakhmetova, Gulnara Svyatova, Galina Berezina, Alexandra Murtazaliyeva

PMC · DOI: 10.34763/jmotherandchild.20252901.d-25-00019 · Journal of Mother and Child · 2025-11-14

## TL;DR

This study identifies genetic markers linked to pre-eclampsia and cerebral complications in Kazakh women, which could help in early detection and treatment.

## Contribution

The study reports novel associations between immune and lipid metabolism genes and pre-eclampsia in a Central Asian population.

## Key findings

- Genes TLR4, PLEKHA1, PLEKHG1, APOE, FTO, and LPL were found to be in genetic equilibrium in the Kazakh sample.
- Minor allele frequencies for these genes suggest potential roles in pre-eclampsia and cerebral complications.
- The findings may aid in developing personalized prevention and treatment strategies for pre-eclampsia.

## Abstract

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.

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.

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%.

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.

## Linked entities

- **Genes:** TLR4 (toll like receptor 4) [NCBI Gene 7099], PLEKHA1 (pleckstrin homology domain containing A1) [NCBI Gene 59338], PLEKHG1 (pleckstrin homology and RhoGEF domain containing G1) [NCBI Gene 57480], APOE (apolipoprotein E) [NCBI Gene 348], FTO (FTO alpha-ketoglutarate dependent dioxygenase) [NCBI Gene 79068], LPL (lipoprotein lipase) [NCBI Gene 4023]
- **Diseases:** pre-eclampsia (MONDO:0005081)

## Full-text entities

- **Genes:** FTO (FTO alpha-ketoglutarate dependent dioxygenase) [NCBI Gene 79068] {aka ALKBH9, BMIQ14, GDFD, IFEX9}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, PLEKHG1 (pleckstrin homology and RhoGEF domain containing G1) [NCBI Gene 57480] {aka ARHGEF41}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, PLEKHA1 (pleckstrin homology domain containing A1) [NCBI Gene 59338] {aka TAPP1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}
- **Diseases:** Pre-Eclampsia (MESH:D011225), Acute Cerebral Circulatory Failure (MESH:D012769)
- **Chemicals:** Lipid (MESH:D008055)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** rs9478812, rs4986790, rs285, rs1421085, rs2281673, rs7412

## Full text

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## References

35 references — full list in the complete paper: https://tomesphere.com/paper/PMC12626190/full.md

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Source: https://tomesphere.com/paper/PMC12626190