Paraoxonase 1 gene and glutathione S-transferase μ 1 gene interaction with preterm delivery in Korean women

Am J Obstet Gynecol. 2010 Dec;203(6):569.e1-7. doi: 10.1016/j.ajog.2010.07.029.

Abstract

Objective: This study was undertaken to identify the paraoxonase 1 gene and glutathione S-transferase μ 1 gene interaction for the risk of preterm delivery and to determine the serum paraoxonase activity according to paraoxonase 1 genotypes.

Study design: This case-control study was performed on 162 gravida women with preterm delivery and 306 controls. Serum paraoxonase activity was measured by a ultraviolet spectrophotometer. Logistic regression, 2-way analysis of variance, and multifactor dimensionality reduction analysis were used.

Results: Gravida women with the QQ and QR genotype of paraoxonase 1 with high body mass index had 6.19- and 4.41-fold increased risks of preterm delivery. The glutathione S-transferase μ 1 null genotype and the interaction between the paraoxonase 1 genotype and glutathione S-transferase μ 1 null type conferred a risk for preterm delivery. Serum paraoxonase activity was significantly different according to paraoxonase 1 genotypes (P < .0001).

Conclusion: The glutathione S-transferase μ 1 null genotype confers a risk for preterm delivery in Korean gravida women independent of and interactive with the paraoxonase 1 genotype.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aryldialkylphosphatase / genetics*
  • Asian People / genetics*
  • Case-Control Studies
  • Confidence Intervals
  • Female
  • Gene Expression Regulation, Developmental
  • Genetic Predisposition to Disease / ethnology
  • Genotype
  • Gestational Age
  • Glutathione Transferase / genetics*
  • Humans
  • Korea
  • Logistic Models
  • Multivariate Analysis
  • Odds Ratio
  • Polymorphism, Genetic
  • Pregnancy
  • Premature Birth / genetics*
  • Reference Values
  • Risk Assessment
  • Sensitivity and Specificity

Substances

  • Glutathione Transferase
  • Aryldialkylphosphatase