Literature DB >> 32607660

Efficacy of febuxostat versus allopurinol and the predictors of achieving target serum urate in a cohort of Thai people with gout.

Ratchaya Lertnawapan1, Kanon Jatuworapruk2.   

Abstract

OBJECTIVE: The objectives of our study were to compare the efficacy of febuxostat with allopurinol in Thai subjects with gout, as well as to determine the predictive factors of responsiveness to urate-lowering agents and to evaluate the safety of febuxostat in a real-world setting.
METHODS: The study was a retrospective cohort study; a total of 354 gout patients were recruited from February 2015 to November 2018. The patients were categorized according to prescription of allopurinol or febuxostat. Demographic data, comorbidities, concomitant medications, gout-related clinical parameters, and the laboratory results were collected. The serial serum urate (sUA) levels were recorded at the beginning of the treatment (baseline), and after treatment at 12 weeks, 18 weeks, and 27 weeks. The primary efficacy endpoint was the achievement of target urate of < 6 mg/dl in people taking febuxostat, compared with those taking allopurinol. The secondary endpoints were the predictive factors of achieving target urate level and adverse drug reactions in patients taking febuxostat. Multivariable regression analysis was used to determine factors associated with achieving target serum urate.
RESULTS: After the treatment, the febuxostat groups had significantly lower mean sUA compared with the allopurinol groups across all follow-up periods. The proportion of people who achieved target serum urate was also higher in the febuxostat groups compared with the allopurinol groups throughout the follow-up periods. The multivariable regression analysis showed that febuxostat 40 mg (OR = 10.96 (95% CI 4.32-27.80); p value < 0.001), febuxostat 80 mg (OR = 9.54 (95% CI 3.91-23.28), smoking (OR = 2.35 (95% CI 1.13-4.91); p value = 0.023), and low baseline serum urate (OR = 0.62 (95% CI 0.52-0.74); p value < 0.001) were associated with the achievement of target serum urate. No adverse drug reaction from febuxostat was observed even among people with renal insufficiency.
CONCLUSION: In a Thai cohort, people receiving febuxostat are more likely to achieve target serum urate level, compared with people receiving allopurinol. Febuxostat (40 or 80 mg), smoking, and low baseline serum urate were associated with the achievement of target serum urate. KEY POINTS: • Febuxostat showed superior urate-lowering efficacy compared with allopurinol in an Asian population. • In addition to febuxostat, lower baseline serum urate level and history of smoking were associated with achieving target serum urate in gout patients.

Entities:  

Keywords:  Allopurinol; Febuxostat; Gout; Urate-lowering therapy; Uric acid

Mesh:

Substances:

Year:  2020        PMID: 32607660     DOI: 10.1007/s10067-020-05262-6

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  29 in total

1.  Febuxostat Therapy for Patients With Stage 3 CKD and Asymptomatic Hyperuricemia: A Randomized Trial.

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Journal:  Am J Kidney Dis       Date:  2018-09-01       Impact factor: 8.860

2.  Changes in the Presentation of Incident Gout and the Risk of Subsequent Flares: A Population-based Study over 20 Years.

Authors:  Mohanad M Elfishawi; Nour Zleik; Zoran Kvrgic; Clement J Michet; Cynthia S Crowson; Eric L Matteson; Tim Bongartz
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3.  The urate-lowering efficacy and safety of febuxostat in the treatment of the hyperuricemia of gout: the CONFIRMS trial.

Authors:  Michael A Becker; H Ralph Schumacher; Luis R Espinoza; Alvin F Wells; Patricia MacDonald; Eric Lloyd; Christopher Lademacher
Journal:  Arthritis Res Ther       Date:  2010-04-06       Impact factor: 5.156

4.  Major Cardiovascular Events in Patients with Gout and Associated Cardiovascular Disease or Heart Failure and Chronic Kidney Disease Initiating a Xanthine Oxidase Inhibitor.

Authors:  JoAnne Foody; Robin S Turpin; Beni A Tidwell; Debra Lawrence; Kathy L Schulman
Journal:  Am Health Drug Benefits       Date:  2017-11

Review 5.  Current Perspectives on Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis.

Authors:  Marianne Lerch; Carlo Mainetti; Benedetta Terziroli Beretta-Piccoli; Thomas Harr
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6.  Comparative effectiveness of urate lowering with febuxostat versus allopurinol in gout: analyses from large U.S. managed care cohort.

Authors:  Jasvinder A Singh; Kasem S Akhras; Aki Shiozawa
Journal:  Arthritis Res Ther       Date:  2015-05-12       Impact factor: 5.156

7.  Gout is associated with a higher risk of chronic renal disease in older adults: a retrospective cohort study of U.S. Medicare population.

Authors:  Jasvinder A Singh; John D Cleveland
Journal:  BMC Nephrol       Date:  2019-03-15       Impact factor: 2.388

8.  The anatomical pathology of gout: a systematic literature review.

Authors:  Patapong Towiwat; Ashika Chhana; Nicola Dalbeth
Journal:  BMC Musculoskelet Disord       Date:  2019-04-01       Impact factor: 2.362

9.  Febuxostat does not delay progression of carotid atherosclerosis in patients with asymptomatic hyperuricemia: A randomized, controlled trial.

Authors:  Atsushi Tanaka; Isao Taguchi; Hiroki Teragawa; Nobukazu Ishizaka; Yumiko Kanzaki; Hirofumi Tomiyama; Masataka Sata; Akira Sezai; Kazuo Eguchi; Toru Kato; Shigeru Toyoda; Ryoichi Ishibashi; Kazuomi Kario; Tomoko Ishizu; Shinichiro Ueda; Koji Maemura; Yukihito Higashi; Hirotsugu Yamada; Mitsuru Ohishi; Kotaro Yokote; Toyoaki Murohara; Jun-Ichi Oyama; Koichi Node
Journal:  PLoS Med       Date:  2020-04-22       Impact factor: 11.069

Review 10.  2016 updated EULAR evidence-based recommendations for the management of gout.

Authors:  P Richette; M Doherty; E Pascual; V Barskova; F Becce; J Castañeda-Sanabria; M Coyfish; S Guillo; T L Jansen; H Janssens; F Lioté; C Mallen; G Nuki; F Perez-Ruiz; J Pimentao; L Punzi; T Pywell; A So; A K Tausche; T Uhlig; J Zavada; W Zhang; F Tubach; T Bardin
Journal:  Ann Rheum Dis       Date:  2016-07-25       Impact factor: 19.103

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