The paraoxonase polymorphism in a Saudi Arabian population

Pharmacogenetics. 1993 Jun;3(3):144-9. doi: 10.1097/00008571-199306000-00004.

Abstract

The paraoxonase polymorphism was analysed in the serum of 248 individuals from Saudi Arabia. The phenotyping method used was one based on the ratio of paraoxonase/arylesterase, described in earlier studies. The distribution of this ratio in the sample was trimodal and it provided a good resolution for the identification of three phenotypes: A-homozygotes with low activity; B-homozygotes with high activity; AB-the corresponding heterozygotes, with intermediate activity. Gene frequencies were 0.7296 for the allele A with low activity and 0.2704 for the allele B with high activity. These frequencies are close to those observed in Caucasian samples from North America and Europe. Phenotypic frequencies in the sample fit the Hardy-Weinberg equilibrium.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aryldialkylphosphatase
  • Carboxylic Ester Hydrolases / blood
  • Female
  • Gene Frequency
  • Homozygote
  • Humans
  • Male
  • Middle Aged
  • Phenotype
  • Phosphoric Monoester Hydrolases / blood
  • Phosphoric Monoester Hydrolases / genetics*
  • Polymorphism, Genetic*
  • Saudi-Arabien

Substances

  • Carboxylic Ester Hydrolases
  • arylesterase
  • Phosphoric Monoester Hydrolases
  • Aryldialkylphosphatase