Effect of urate‐lowering therapy on the velocity of size reduction of tophi in chronic gout

Objective The optimal serum urate levels necessary for elimination of tissue deposits of monosodium urate in patients with chronic gout is controversial. This observational, prospective study evaluates the relationship between serum urate levels during therapy and the velocity of reduction of tophi...

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Veröffentlicht in:Arthritis and rheumatism 2002-08, Vol.47 (4), p.356-360
Hauptverfasser: Perez‐Ruiz, Fernando, Calabozo, Marcelo, Pijoan, Jose I., Herrero‐Beites, Ana M., Ruibal, Ana
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Sprache:eng
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Zusammenfassung:Objective The optimal serum urate levels necessary for elimination of tissue deposits of monosodium urate in patients with chronic gout is controversial. This observational, prospective study evaluates the relationship between serum urate levels during therapy and the velocity of reduction of tophi in patients with chronic tophaceous gout. Method Sixty‐three patients with crystal‐confirmed tophaceous gout were treated with allopurinol, benzbromarone, or combined therapy to achieve serum uric acid levels less than the threshold for saturation of urate in tissues. The tophi targeted for evaluation during followup were the largest in diameter found during physical examination. Results Patients taking benzbromarone alone or combined allopurinol and benzbromarone therapy achieved faster velocity of reduction of tophi than patients taking allopurinol alone. The velocity of tophi reduction was linearly related to the mean serum urate level during therapy. The lower the serum urate levels, the faster the velocity of tophi reduction. Conclusion Serum urate levels should be lowered enough to promote dissolution of urate deposits in patients with tophaceous gout. Allopurinol and benzbromarone are equally effective when optimal serum urate levels are achieved during therapy. Combined therapy may be useful in patients who do not show enough reduction in serum urate levels with single‐drug therapy.
ISSN:0004-3591
0893-7524
1529-0131
1529-0123
DOI:10.1002/art.10511