Demonstration of slow acetylator genotype of N-acetyltransferase in isoniazid neuropathy using an archival hematoxylin and eosin section of a sural nerve biopsy specimen

J Neurol Sci. 1996 Jan;135(1):51-4. doi: 10.1016/0022-510x(95)00254-y.

Abstract

The genotype for N-acetyltransferase was analyzed in five Japanese patients with isoniazid neuropathy by using the allele specific polymerase chain reaction for a single slice of the 30-year-old paraffin-embedded and hematoxylin-eosin stained sural nerve biopsy specimens. We found slow acetylator genotypes for N-acetyltransferase in all isoniazid neuropathy patients. This result confirmed that patients with the slow acetylator genotype tend to develop neuropathy after administration of isoniazid.

MeSH terms

  • Acetylation / drug effects
  • Alleles
  • Antitubercular Agents / adverse effects*
  • Arylamine N-Acetyltransferase / genetics
  • Arylamine N-Acetyltransferase / metabolism*
  • Base Sequence
  • Biopsy
  • DNA Primers / genetics
  • Eosine Yellowish-(YS)
  • Genotype
  • Hematoxylin
  • Humans
  • Isoniazid / adverse effects*
  • Mutation / physiology
  • Paraffin Embedding
  • Peripheral Nervous System Diseases / chemically induced
  • Peripheral Nervous System Diseases / enzymology
  • Peripheral Nervous System Diseases / genetics*
  • Polymerase Chain Reaction
  • Sural Nerve / enzymology*
  • Sural Nerve / physiopathology
  • Time Factors

Substances

  • Antitubercular Agents
  • DNA Primers
  • Arylamine N-Acetyltransferase
  • Eosine Yellowish-(YS)
  • Isoniazid
  • Hematoxylin