The effect of folic acid and folinic acid supplements on purine metabolism in methotrexate‐treated rheumatoid arthritis
Open Access
- 8 October 2004
- journal article
- clinical trial
- Published by Wiley in Arthritis & Rheumatism
- Vol. 50 (10) , 3104-3111
- https://doi.org/10.1002/art.20516
Abstract
Objective To determine if folinic acid supplementation during methotrexate (MTX) therapy for rheumatoid arthritis (RA) reduces both urinary 5‐aminoimidazole‐4‐carboxamide (AICA) and urinary adenosine excretion more than does folic acid supplementation. AICA and adenosine are markers for MTX interference with purine metabolism. Methods Forty patients with RA who received MTX for 6 weeks were randomized to receive either daily folic acid or folinic acid supplements during an additional week of MTX therapy. Colorimetric and radioimmunocompetition assays were used to measure 24‐hour urinary AICA and adenosine excretion levels, respectively. Results At the end of 6 weeks, 24‐hour urinary levels of AICA, but not adenosine, were elevated as compared with baseline levels (i.e., prior to MTX therapy). Folinic acid, but not folic acid, supplementation normalized urinary AICA levels during MTX therapy. Relatively high urinary levels of AICA were correlated with reduced disease activity. No similar correlations were seen with urinary adenosine levels. Conclusion The blockade of purine nucleotide biosynthesis by MTX at the AICA ribonucleotide transformylase–catalyzed step may be related to the efficacy of MTX, and this blockade is effectively relieved by folinic acid, but not by folic acid, supplementation.Keywords
Funding Information
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (P60-AR-40895)
- Office of Dietary Supplements (1R29-AR-42674)
- Department of Research Resources Clinical Research Center (M01-RR-00032)
- NIH
This publication has 33 references indexed in Scilit:
- Anti-inflammatory mechanisms of methotrexate in rheumatoid arthritisAnnals of the Rheumatic Diseases, 2001
- Anti-arthritic effect of methotrexate: is it really mediated by adenosine?European Journal of Pharmaceutical Sciences, 2000
- THE MECHANISM OF ACTION OF METHOTREXATERheumatic Disease Clinics of North America, 1997
- Molecular therapeutics. Methotrexate and its mechanism of actionArthritis & Rheumatism, 1996
- Adenosine, an endogenous anti-inflammatory agentJournal of Applied Physiology, 1994
- The antiinflammatory mechanism of methotrexate. Increased adenosine release at inflamed sites diminishes leukocyte accumulation in an in vivo model of inflammation.Journal of Clinical Investigation, 1993
- Methotrexate inhibits neutrophil function by stimulating adenosine release from connective tissue cells.Proceedings of the National Academy of Sciences, 1991
- The american rheumatism association 1987 revised criteria for the classification of rheumatoid arthritisArthritis & Rheumatism, 1988
- Inhibition of 5-aminoimidazole-4-carboxamide ribotide transformylase, adenosine deaminase and 5′-adenylate deaminase by polyglutamates of methotrexate and oxidized folates and by 5-aminoimidazole-4-carboxamide riboside and ribotideBiochemical Journal, 1986
- Assessment of patient satisfaction in activities of daily living using a modified stanford health assessment questionnaireArthritis & Rheumatism, 1983