Relation of locus 1p13 rs646776 polymorphism with the risk of preeclampsia

Hypertens Pregnancy. 2018 May;37(2):81-86. doi: 10.1080/10641955.2018.1454462. Epub 2018 Mar 25.

Abstract

Objective: This study aimed to assess the relation of locus 1p13 rs646776 (T/C) polymorphism with preeclampsia in Egyptian women.

Methods: The study included 100 healthy pregnant female subjects and 100 preeclampsia patients. The genotypes of the polymorphisms were assessed. Endothelin-1 level was determined in plasma.

Results: The major T allele of the 1p13.3 genomic region rs646776 polymorphism had a higher frequency in preeclampsia patients. Carriers of C allele had significantly lower endothelin-1 levels, lower systolic and diastolic blood pressure, decreased proteinuria, and increased HDL-C in the patients.

Conclusion: The rare C allele of rs646776 polymorphism in chromosomal locus 1p13.3 is associated with decreased risk of preeclampsia.

Keywords: Endothelin-1; preeclampsia; rs646776.

MeSH terms

  • Adult
  • Alleles*
  • Chromosomes, Human, Pair 1*
  • Female
  • Gene Frequency
  • Genetic Loci*
  • Genetic Predisposition to Disease*
  • Genotype
  • Humans
  • Polymorphism, Genetic
  • Pre-Eclampsia / genetics*
  • Pregnancy
  • Young Adult