Abnormal sulphur oxidation in systemic lupus erythematosus

Lancet. 1992 Jan 4;339(8784):25-6. doi: 10.1016/0140-6736(92)90144-r.

Abstract

S-carboxy-L-methylcysteine was used to assess the activity of the S-oxidation pathway of sulphur metabolism in 35 patients with systemic lupus erythematosus (SLE); 25 (71%) showed impaired sulphoxidation and 21 (60%) produced virtually no sulphoxides, compared with 17 (36%) and 2 (4%), respectively, of 47 healthy controls. The substrate/product ratio of cysteine oxygenase (plasma cysteine/sulphate) was significantly higher in SLE patients than in controls (median [interquartile range] 362 [224-588] vs 65 [44-111]; p less than 0.00001). The alternative pathway of sulphur metabolism, S-methylation, catalysed by thiolmethyltransferase, was not impaired in the SLE patients. There is a biochemical difference in sulphur metabolism between SLE and rheumatoid arthritis, since both pathways are impaired in the latter disorder.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Aged
  • Carbocysteine / metabolism*
  • Cysteine Dioxygenase
  • Dioxygenases*
  • Humans
  • Lupus Erythematosus, Systemic / enzymology
  • Lupus Erythematosus, Systemic / metabolism*
  • Methyltransferases / metabolism*
  • Middle Aged
  • Oxidation-Reduction
  • Oxygenases / blood
  • Sulfates / blood
  • Sulfur / metabolism*

Substances

  • Sulfates
  • Sulfur
  • Carbocysteine
  • Oxygenases
  • Dioxygenases
  • Cysteine Dioxygenase
  • Methyltransferases
  • thiol S-methyltransferase