An insertion-deletion polymorphism in interleukin-1α gene associated with susceptibility to preeclampsia

Hypertens Pregnancy. 2014 Nov;33(4):395-401. doi: 10.3109/10641955.2014.915034. Epub 2014 May 19.

Abstract

Objective: To determine whether preeclampsia is associated with polymorphisms in the IL-1α.

Methods: We genotyped a Chinese population (212 women with preeclampsia and 203 controls) for the polymorphism of the interleukin-1α gene (3'-untranslated region). Clinical data were collected from medical records.

Results: Significantly reduced preeclampsia risk was found to be associated with both I allele (p < 0.001, OR = 0.487, CI = 0.360-0.658) and I/I genotype (p < 0.01, OR = 0.26, CI = 0.13-0.55) of the rs3783553 polymorphisms.

Conclusion: The "TTCA" insertion allele of rs3783553 contributes to reduce the individual's susceptibility for preeclampsia, which implies that the insertion allele is a protective factor for the preeclampsia development.

Keywords: IL-α; Polymorphism; Preeclampsia; Susceptibility..

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Asian People / genetics
  • Case-Control Studies
  • China
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • INDEL Mutation
  • Interleukin-1alpha / genetics*
  • Middle Aged
  • Pre-Eclampsia / genetics*
  • Pregnancy
  • Young Adult

Substances

  • Interleukin-1alpha