D-Penicillamine induced toxicity in rheumatoid arthritis: the role of sulphoxidation status and HLA-DR3

J Rheumatol. 1984 Oct;11(5):626-32.

Abstract

Sulphoxidation of carbocysteine, a drug structurally similar to D-penicillamine, displays a skewed distribution within a population. In 66 patients with rheumatoid arthritis (RA) a significant association between impaired sulphoxidation and toxicity (p less than 0.001) was found; HLA-DR3, although associated with toxicity (p less than 0.05), appeared to be an independent risk factor of most importance in the group with extensive sulphoxidation. The relative risk of toxicity in a patient possessing either DR3 or impaired sulphoxidation was 25. The prevalence of poor sulphoxidizers within this group of RA patients was increased compared to that in a previous population study and requires further investigation. Our findings explain a number of the toxic phenomena associated with D-penicillamine administration in RA.

MeSH terms

  • Adult
  • Aged
  • Arthritis, Rheumatoid / drug therapy*
  • Arthritis, Rheumatoid / genetics
  • Arthritis, Rheumatoid / metabolism
  • Biotransformation
  • Carbocysteine / metabolism*
  • Cysteine / analogs & derivatives*
  • Female
  • HLA-DR3 Antigen
  • HLA-DR4 Antigen
  • Histocompatibility Antigens Class II / genetics*
  • Humans
  • Male
  • Middle Aged
  • Penicillamine / adverse effects*
  • Penicillamine / metabolism
  • Penicillamine / therapeutic use
  • Risk

Substances

  • HLA-DR3 Antigen
  • HLA-DR4 Antigen
  • Histocompatibility Antigens Class II
  • Carbocysteine
  • Penicillamine
  • Cysteine