A simplified assay for the arylamine N-acetyltransferase 2 polymorphism validated by phenotyping with isoniazid

J Med Genet. 1997 Sep;34(9):758-60. doi: 10.1136/jmg.34.9.758.

Abstract

Human arylamine N-acetyltransferase (NAT) activity is determined by two distinct genes, NAT1 and NAT2, and the classical acetylation polymorphism in NAT2 has been associated with a variety of disorders, including lupus erythematosus and arylamine induced cancers. Over 50% of the white population exhibit a slow acetylator phenotype. The genetic basis of the defect has been identified and several DNA based assays are available for genotyping studies. We present here a simplified, rapid PCR based assay for the identification of the major slow acetylator genotypes and validate it using isoniazid as probe drug. This assay was 100% predictive of phenotype. The three genotypes (homozygous mutated, heterozygous, and homozygous rapid) corresponded to a trimodal distribution of Ac-INH/INH metabolic ratios (slow, intermediate, and rapid) without overlapping.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arylamine N-Acetyltransferase / genetics*
  • Humans
  • Isoniazid / therapeutic use*
  • Phenotype
  • Polymerase Chain Reaction / methods*
  • Polymorphism, Genetic*
  • Scotland
  • Sweden

Substances

  • Arylamine N-Acetyltransferase
  • Isoniazid