Benzbromarone in the treatment of gout

被引:151
作者
Azevedo, Valderilio Feijo [1 ,2 ]
Kos, Igor Age [2 ]
Vargas-Santos, Ana Beatriz [3 ]
Castelar Pinheiro, Geraldo da Rocha [3 ]
Paiva, Eduardo dos Santos [1 ]
机构
[1] Univ Fed Parana, Rua Gen Carneiro 181, Curitiba, Parana, Brazil
[2] Edumed Educ Saude, Rua Bispo Dom Jose 2495, Curitiba, Parana, Brazil
[3] Univ Estado Rio De Janeiro, Rio De Janeiro, Brazil
关键词
EPOXIDE-DERIVED METABOLITE(S); URATE-LOWERING THERAPY; CHRONIC KIDNEY-DISEASE; PEROXISOME PROLIFERATION; URIC-ACID; EFFICACY; HYPERURICEMIA; FAILURE; SAFETY; ALLOPURINOL;
D O I
10.1186/s42358-019-0080-x
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Background Benzbromarone is a uricosuric drug that has been used in the treatment of gout over the last 30 years. Due to its potent inhibition of the dominant apical (luminal) urate exchanger in the human proximal tubule URAT1, it reduces the urate reabsorption, diminishing serum urate levels and therefore preventing gout flares. Main body of the abstract Through several clinical trials, Benzbromarone has been proved effective and safe, inclusive in patients with chronic kidney disease and as combination therapy with allopurinol. Due to hepatotoxicity reports, it was withdrawn from the European market by the manufacturer, however many authors have questioned the product's withdrawal due to a lack of clinical evidence in order to support its hepatotoxicity. Benzbromarone is still available in several European countries, New Zealand, Brazil and several other countries. Despite the product's marketing over more than 20 years after the first hepatotoxicity reports, we have found only five reports in our literature search, and no prospective or retrospective study correlating hepatotoxicity with benzbromarone use. Short conclusion Benzbromarone is a safe and effective molecule for the treatment of gout. However, due to in vitro and in vivo data related to hepatotoxicity, it is prudent to prescribe it with some caution, especially for patients with an already known liver condition.
引用
收藏
页数:5
相关论文
共 53 条
[1]
Fulminant hepatic failure associated with benzbromarone treatment: A case report [J].
Arai, M ;
Yokosuka, O ;
Fujiwara, K ;
Kojima, H ;
Kanda, T ;
Hirasawa, H ;
Saisho, H .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2002, 17 (05) :625-626
[2]
Azevedo VF, 2017, REV BRAS REUMATOL, V57, P346, DOI [10.1016/j.rbr.2016.06.009, 10.1016/j.rbre.2017.03.002]
[3]
Allopurinol, Benzbromarone, or a Combination in Treating Patients with Gout: Analysis of a Series of Outpatients [J].
Azevedo, Valderilio Feijo ;
Buiar, Pedro Grachinski ;
Giovanella, Laura Helena ;
Severo, Carolina Rossetti ;
Carvalho, Mauricio .
INTERNATIONAL JOURNAL OF RHEUMATOLOGY, 2014, 2014
[4]
Impact of comorbidities on gout and hyperuricaemia: an update on prevalence and treatment options [J].
Bardin, Thomas ;
Richette, Pascal .
BMC MEDICINE, 2017, 15
[5]
TOXICOLOGICAL STUDIES ON A BENZOFURAN DERIVATIVE .3. COMPARISON OF PEROXISOME PROLIFERATION IN RAT AND HUMAN HEPATOCYTES IN PRIMARY CULTURE [J].
BICHET, N ;
CAHARD, D ;
FABRE, G ;
REMANDET, B ;
GOUY, D ;
CANO, JP .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 106 (03) :509-517
[6]
Bluestone R, 1980, Adv Exp Med Biol, V122A, P283
[7]
TOXICOLOGICAL STUDIES ON A BENZOFURANE DERIVATIVE .2. DEMONSTRATION OF PEROXISOME PROLIFERATION IN RAT-LIVER [J].
BUTLER, EG ;
ICHIDA, T ;
MARUYAMA, H ;
SCHULTEHERMANN, R ;
WILLIAMS, GM .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 106 (03) :500-508
[8]
Castrejon I, 2015, RHEUMATOL INT, V35, P1127, DOI 10.1007/s00296-014-3189-6
[9]
Comparative effectiveness of allopurinol, febuxostat and benzbromarone on renal function in chronic kidney disease patients with hyperuricemia: a 13-year inception cohort study [J].
Chou, Hsu-Wen ;
Chiu, Hsien-Tsai ;
Tsai, Ching-Wei ;
Ting, I-Wen ;
Yeh, Hung-Chieh ;
Huang, Han-Chun ;
Kuo, Chin-Chi .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2018, 33 (09) :1620-1627
[10]
Mechanistic Aspects of Inflammation and Clinical Management of Inflammation in Acute Gouty Arthritis [J].
Cronstein, Bruce N. ;
Sunkureddi, Prashanth .
JCR-JOURNAL OF CLINICAL RHEUMATOLOGY, 2013, 19 (01) :19-29