STOX1 promotor region -922 T>C polymorphism is associated with Early-Onset preeclampsia

Seyda Akin1, Ergun Pinarbasi1, Aslihan Esra Bildirici1,2

  • 1Faculty of Medicine, Department of Medical Biology, Sivas Cumhuriyet University, Sivas, Türkiye.

Insights

Genetic variants in the STOX1 gene promoter are linked to preeclampsia (PE), particularly early-onset PE. This finding highlights STOX1

Area of Science:

  • Genetics
  • Obstetrics
  • Molecular Biology

Background:

  • Preeclampsia (PE) affects 5-8% of pregnancies, posing risks to mother and fetus.
  • The STOX1 gene has known variants associated with PE and HELLP syndrome.
  • Previous research linked STOX1 polymorphisms to early-onset PE.

Purpose of the Study:

  • To investigate the role of STOX1 gene promoter region variants in preeclampsia.
  • To analyze the maternal genotype's effect on STOX1 expression in PE.

Main Methods:

  • Sanger sequencing was used to analyze blood samples from 118 PE patients and 96 healthy pregnant women.
  • Sequence analysis focused on the promoter region of the STOX1 gene.

Main Results:

  • A specific polymorphism, -922 T>C (rs884181), was identified in the STOX1 promoter region.
  • This polymorphism showed a statistically significant association with early-onset PE (p=0.02) and overall PE (p=0.014).

Conclusions:

  • STOX1 promoter variations are significantly associated with preeclampsia, especially early-onset cases.
  • These findings emphasize the importance of STOX1 in PE pathogenesis and disease risk.
  • Further research into STOX1 variations could inform PE prevention and treatment strategies.

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