[Genetic polymorphism and treatment of chronic bowel inflammatory diseases: the example of azathioprine]

Therapie. 2004 Jan-Feb;59(1):71-5. doi: 10.2515/therapie:2004015.
[Article in French]

Abstract

Azathioprine is an immunosuppressive drug used in the treatment of inflammatory bowel disease. It is a prodrug that is hydrolysed to 6-mercaptopurine, which represents the active form. Azathioprine is also used in the treatment of leukaemia in children and in organ transplantation. Azathioprine treatment is associated with adverse effects such as leukopenia and aplasia. These adverse effects are related to a single nucleotide polymorphism, including the inability of cells to synthesize thiopurine methyltransferase (TPMT). TPMT is a detoxification enzyme that limits 6-thioguanine nucleotide production and thereby interferes with normal DNA and RNA synthesis. This review presents the different approaches used for azathioprine therapeutic monitoring in IBD treatment and discusses the discrepancies in recent clinical trials.

Publication types

  • English Abstract
  • Review

MeSH terms

  • Azathioprine / pharmacokinetics*
  • Azathioprine / therapeutic use*
  • Biotransformation
  • Humans
  • Immunosuppressive Agents / pharmacokinetics*
  • Immunosuppressive Agents / therapeutic use*
  • Inflammatory Bowel Diseases / drug therapy*
  • Inflammatory Bowel Diseases / genetics*
  • Methyltransferases / genetics
  • Methyltransferases / metabolism
  • Polymorphism, Genetic / physiology*

Substances

  • Immunosuppressive Agents
  • Methyltransferases
  • thiopurine methyltransferase
  • Azathioprine