Homocysteine levels in patients with rheumatoid arthritis treated with low‐dose methotrexate

Academic Article

Abstract

  • Plasma homocysteine levels were determined in patients who participated in a randomized, double‐blind placebo‐controlled trial of folate supplementation (1 mg/day) during methotrexate therapy for rheumatoid arthritis. Plasma and red blood cell folate levels before methotrexate therapy were significantly negatively correlated with homocysteine levels. Homocysteine levels were not significantly correlated with the initial C1 index (an assay that measures the folate status of blood mononuclear cells) or the C1 index during methotrexate therapy. There was no significant difference in homocysteine levels between pre‐treatment and levels drawn at 3 or 6 months. Initial homocysteine levels were predictive of toxicities, such as gastrointestinal intolerance and elevations of liver enzymes in the placebo group. There was no significant correlation between occurrence of toxicity and initial homocysteine levels in the folic acid‐supplemented group. Homocysteine levels were not predictive of the efficacy of methotrexate therapy. We conclude that plasma homocysteine levels are correlated with plasma and red blood cell folate levels before methotrexate therapy but is not correlated with folate status in blood mononuclear cells. Clinical Pharmacology and Therapeutics (1991) 50, 547–556; doi: © 1991 American Society for Clinical Pharmacology and Therapeutics
  • Authors

    Digital Object Identifier (doi)

    Author List

  • Morgan SL; Baggott JE; Refsum H; Ueland PM
  • Start Page

  • 547
  • End Page

  • 556
  • Volume

  • 50
  • Issue

  • 5–1