Effects of intensive urate lowering therapy with febuxostat in comparison with allopurinol on pulse wave velocity in patients with gout and increased cardiovascular risk: the FORWARD study

Author:

Desideri Giovambattista1,Rajzer Marek2,Gerritsen Martijn3,Nurmohamed Michael T4,Giannattasio Cristina5,Tausche Anne-Kathrin6,Borghi Claudio7ORCID

Affiliation:

1. Department of Life, Health and Environmental Sciences, University of l’Aquila, L’Aquila, Italy

2. I-st Department of Cardiology Interventional Electrocardiology and Arterial Hypertension, Jagiellonian University Medical College, Cracow, Poland

3. Department of Rheumatology, Reade, Amsterdam, The Netherlands

4. Department of Rheumatology, Amsterdam Rheumatology & immunology Center | Reade, Amsterdam, The Netherlands

5. School of Medicine and Surgery, Milano Bicocca University and Cardio Center de Gasperis ASST Niguarda, Milano, Italy

6. Department of Rheumatology, University Clinic Carl Gustav Carus at the TU Dresden, Dresden, Germany

7. Department of Medical and Surgical Sciences, Ospedale Malpighi, University of Bologna, Via Albertoni 15, 40138 Bologna, Italy

Abstract

Abstract Aims Hyperuricaemia and gout are strongly related with traditional cardiovascular risk factors and vascular damage. This study aimed to assess whether febuxostat and allopurinol could differently influence carotid-femoral pulse wave velocity (cfPWV) in patients with gout and elevated serum uric acid (SUA) levels. Methods and results A multi-centre, multinational, phase IV, randomized, parallel-group, active-controlled, open-label trial with blind endpoints evaluation. One hundred and ninety-seven adults with gout and SUA levels ≥8 mg/dL were randomized to febuxostat or allopurinol in a 1:1 ratio for 36 weeks. The primary outcome was the comparison of the effects of febuxostat and allopurinol on changes in cfPWV. The mean cfPWV values at randomization and Week 36 were 8.69 and 9.00 m/s, respectively for subjects randomized to febuxostat and 9.02 and 9.05 m/s for subjects randomized to allopurinol. No statistically significant changes in cfPWV by treatment assignment were observed at any time point for any of the assessed parameters. More subjects who received febuxostat had serum urate concentrations ≤6 mg/dL following treatment (78.3% vs. 61.1% at Week 36, P = 0.0137). Treatment-emergent adverse events were reported by 51 (52.0%) patients randomized to febuxostat and 63 (62.5%) patients randomized to allopurinol. The majority of events were mild in both treatment groups and included gout flares and arthralgia. Conclusion In patients with gout and elevated SUA levels the arterial stiffness remained stable both with febuxostat and allopurinol. Febuxostat was more effective and faster than allopurinol in achieving the SUA target. Both treatments were safe and well tolerated.

Funder

Menarini International Operations Luxembourg

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Cardiology and Cardiovascular Medicine

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