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DOI 10.1001/jamainternmed.2025.8237

Медицинская библиотека · JAMA internal medicine · 2026

Diacerein for Knee Osteoarthritis: A Randomized Clinical Trial.

Aitken Dawn, Cai Guoqi, Hill Catherine L, Cicuttini Flavia M, Wluka Anita E, Wang Yuanyuan, Keen Helen I, Thompson Michael J W, Asthana Chhavi, Antony Benny E, Wang Xia, Winzenberg Tania, de Graaff Barbara, Buttigieg Kathy, Otahal Petr, Jones Graeme

СтатьяРандомизированное исследованиеМногоцентровое исследованиеПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

IMPORTANCE

Knee osteoarthritis (OA) is disabling, with few effective treatments. Anti-inflammatory treatments may be effective for patients with an inflammatory phenotype.

OBJECTIVES

To evaluate the efficacy of the interleukin-1β blocker diacerein, compared with placebo, on knee pain in people with knee OA who have substantial knee pain and inflammation (effusion-synovitis on magnetic resonance imaging).

DESIGN, SETTING, AND

PARTICIPANTS

This multicenter, randomized, double-blind, placebo-controlled clinical trial was conducted in 4 Australian centers. Participants with clinical knee OA, substantial knee pain, and effusion-synovitis on magnetic resonance imaging were enrolled from June 2019 to September 2022. Final follow-up occurred on February 6, 2023. Data analysis began on July 7, 2023.

INTERVENTIONS: Participants were randomized (1:1) to diacerein, 50 mg, once daily or identical placebo for the first 2 weeks, which increased to 50 mg, twice daily until 24 weeks if adverse effects were tolerable.

MAIN OUTCOMES AND MEASURES: The primary outcome was change in knee pain as assessed by the visual analogue scale (range, 0-100 mm; minimal clinically important improvement, 15) over 24 weeks.

RESULTS

Of 262 participants randomized (mean [SD] age, 54.9 [6.1] years; 147 [56.1%] female and 115 [43.9%] male), 231 (88.2%) completed the trial. Compared with placebo, diacerein did not improve knee pain over 24 weeks (-19.9 mm [diacerein] vs -18.6 mm [placebo]; between-group mean difference, -1.3 mm; 95% CI, -9.8 to 7.3). The most common adverse events were gastrointestinal symptoms, which occurred in 55 participants (41.7%) in the diacerein group and 33 (25.4%) in the placebo group, most commonly diarrhea (51 [38.6%] in the diacerein group vs 29 [22.3%] in the placebo group). Change in urine color was observed among 13 participants (9.8%) who received diacerein.

CONCLUSIONS AND RELEVANCE: This randomized clinical trial found that, in patients with symptomatic knee OA and effusion-synovitis, diacerein (50 mg, twice daily) over 24 weeks resulted in no greater improvement in knee pain compared with placebo. These findings do not support diacerein for treating knee pain in this population.

TRIAL REGISTRATION: Australian New Zealand Clinical Trials Registry: ACTRN12618001656224.

Для цитирования: Aitken Dawn, Cai Guoqi, Hill Catherine L, Cicuttini Flavia M, Wluka Anita E, Wang Yuanyuan, Keen Helen I, Thompson Michael J W, Asthana Chhavi, Antony Benny E, Wang Xia, Winzenberg Tania, de Graaff Barbara, Buttigieg Kathy, Otahal Petr, Jones Graeme. Diacerein for Knee Osteoarthritis: A Randomized Clinical Trial.. JAMA internal medicine. 2026. DOI: 10.1001/jamainternmed.2025.8237.

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