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Low-dose methotrexate compared with auranofin in adult rheumatoid arthritis: a thirty-six-week, double-blind trial

Authors :
Weinblatt, Michael E.
Kaplan, Herbert
Germain, Bernard F.
Merriman, Richard C.
Solomon, Sheldon D.
Wall, Bruce
Anderson, Larry
Block, Sidney
Irby, Robert
Wolfe, Frederick
Gall, Eric
Torretti, Dennis
Biundo, Joseph
Small, Ralph
Coblyn, Jon
Polisson, Richard
Source :
Arthritis and Rheumatism. March, 1990, Vol. 33 Issue 3, p330, 9 p.
Publication Year :
1990

Abstract

Several studies have shown that the drug methotrexate is effective in treating rheumatoid arthritis, an inflammatory joint disease, particularly in patients who are not responsive to conventional therapy. Methotrexate treatment is associated with sustained effectiveness, a decrease in the dose of corticosteroids needed to counteract inflammation, tolerable levels of toxicity, and improved measures of disease severity, such as the erythrocyte sedimentation rate. Studies have shown that methotrexate is more effective and causes more rapid improvement than another agent, azathioprine, used to treat rheumatoid arthritis. The effectiveness of methotrexate was compared with that of the drug auranofin in 281 patients with active rheumatoid arthritis over a 36-week period. Both drugs were effective in treating rheumatoid arthritis, although the effect of methotrexate was greater and occurred earlier than that of auranofin. Methotrexate caused significantly greater improvement in terms of alleviating pain and swelling of joints and reducing disease activity, as assessed by patients and physicians. Auranofin caused more adverse effects and a greater frequency of patients withdrawing from the study due to toxicity of the drug. The findings suggest that methotrexate is more effective and better tolerated than auranofin. (Consumer Summary produced by Reliance Medical Information, Inc.)

Details

ISSN :
00043591
Volume :
33
Issue :
3
Database :
Gale General OneFile
Journal :
Arthritis and Rheumatism
Publication Type :
Periodical
Accession number :
edsgcl.10459736