Azathioprine myelosuppression in multiple sclerosis: characterizing thiopurine methyltransferase polymorphisms

Mult Scler. 2006 Feb;12(1):108-11. doi: 10.1191/135248506ms1249cr.

Abstract

We describe two multiple sclerosis patients who developed pancytopenia following treatment with azathioprine. They were found to have the homozygous polymorphism for thiopurine methyltransferase deficiency and recovered after cessation of drug therapy. We review the literature concerning this molecular derangement and underscore the importance of performing surveillance testing for allelic characterization prior to treatment intervention with this agent for immune-mediated disorders.

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Azathioprine / adverse effects*
  • Female
  • Genetic Variation
  • Homozygote
  • Humans
  • Immunosuppressive Agents / adverse effects
  • Methyltransferases / genetics*
  • Middle Aged
  • Multiple Sclerosis / blood
  • Multiple Sclerosis / drug therapy*
  • Multiple Sclerosis / enzymology
  • Multiple Sclerosis / genetics*
  • Pancytopenia / chemically induced*
  • Polymorphism, Genetic*

Substances

  • Immunosuppressive Agents
  • Methyltransferases
  • thiopurine methyltransferase
  • Azathioprine