39Drug TargeT InsIghTs 2014:8 Open Access: Full open access to this and thousands of other papers at http://www.la-press.com. Drug Target Insights Febuxostat for Hyperuricemia in Patients with Advanced Chronic Kidney Disease Tetsu akimoto1,2, Yoshiyuki Morishita1,3,4, Chiharu Ito1,3,4, Osamu Iimura3, sadao Tsunematsu4, Yuko Watanabe1, eiji Kusano1 and Daisuke nagata1 1Division of Nephrology, Department of Internal Medicine, Jichi Medical University, Tochigi, Japan. 2Green Town Clinic, Tochigi, Japan. 3Kumakura Clinic, Tochigi, Japan. 4Yuki Clinic, Ibaraki, Japan. A BSTR ACT: Febuxostat is a nonpurine xanthine oxidase (XO) inhibitor, which recently received marketing approval. However, information regarding the experience with this agent among advanced chronic kidney disease (CKD) patients is limited. In the current study, we investigated the effects of oral febuxostat in patients with advanced CKD with asymptomatic hyperuricemia. We demonstrated, for the first time, that not only the serum levels of uric acid (UA) but also those of 8-hydroxydeoxyguanosine, an oxidative stress marker, were significantly reduced after six months of febuxostat treatment, with no adverse events. These results encouraged us to pursue further investigations regarding the clinical impact of lowering the serum UA levels with febuxostat in advanced CKD patients in terms of concomitantly reducing oxidative stress via the blockade of XO. More detailed studies with a larger number of subjects and assessments of the effects of multiple factors affecting hyperuricemia, such as age, sex, and dietary habits, would shed light on the therapeutic challenges of treating asymptomatic hyperuricemia in patients with various stages of CKD. K E Y WOR DS: febuxostat, chronic kidney disease, hemodialysis, uric acid, oxidative stress CITATION: akimoto et al. Febuxostat for hyperuricemia in Patients with advanced Chronic Kidney Disease. Drug Target Insights 2014:8 39–43 doi:10.4137/DTI.s16524. RECEIVED: april 28, 2014. RESUBMITTED: June 27, 2014. ACCEPTED FOR PUBLICATION: July 1, 2014. ACADEMIC EDITOR: anuj Chauhan, editor in Chief TYPE: rapid Communication FUNDING: authors disclose no funding sources. COMPETING INTERESTS: Authors disclose no potential conflicts of interest. COPYRIGHT: © the authors, publisher and licensee Libertas academica Limited. This is an open-access article distributed under the terms of the Creative Commons CC-BY-nC 3.0 License. CORRESPONDENCE: tetsu-a@jichi.ac.jp This paper was subject to independent, expert peer review by a minimum of two blind peer reviewers. all editorial decisions were made by the independent academic editor. all authors have provided signed confirmation of their compliance with ethical and legal obligations including (but not limited to) use of any copyrighted material, compliance with ICMJE authorship and competing interests disclosure guidelines and, where applicable, compliance with legal and ethical guidelines on human and animal research participants. Introduction Hyperuricemia, defined as a serum urate level exceeding the limit of solubility, mirrors supersaturation of the extracellu- lar fluid with urate, and predisposes affected subjects to gout, which is characterized by the tissue deposition of monosodium urate crystals, although it is a necessary but not a substantial factor for the development of the disease.1 The current urate- lowering strategies include reducing the urate production with xanthine oxidase (XO) inhibitors and accelerating the urinary excretion of uric acid (UA) with uricosuric agents.2,3 Uricosuric agents, such as probenecid and benzbromarone, may have lim- ited effectiveness in patients with reduced renal function.3,4 The purine analog XO inhibitor, allopurinol, has remained widely prescribed for the treatment of hyperuricemia, but requires dose adjustment in subjects with renal impairment, which may lead to a reduced benefit.2,3,5,6 Febuxostat, a nonpurine XO inhibitor that recently received marketing approval, has been focused on as an alternative option for the treatment of hyperuricemia in patients with chronic kidney disease (CKD) because it undergoes hepatic metabolism and may require less dose adjustment in asso- ciation with the renal function.6,7  Moreover, several lines of evidence have focused on the blockade of XO activity as a potential therapeutic strategy for various other kinds of oxida- tive stress-mediated tissue and vascular injuries.8,9  However, information regarding the experience with this therapeutic agent among patients with advanced CKD is limited.7 In this regard, the current study investigated the effects of febuxostat http://www.la-press.com/drug-target-insights-journal-j23 http://www.la-press.com http://www.la-press.com http://www.la-press.com/drug-target-insights-journal-j23 http://dx.doi.org/10.4137/DTI.S16524 http://creativecommons.org/licenses/by-nc/3.0/ http://creativecommons.org/licenses/by-nc/3.0/ mailto:tetsu-a@jichi.ac.jp Akimoto et al 40 Drug TargeT InsIghTs 2014:8 in patients with advanced CKD with hyperuricemia in terms of the reduction of the serum UA levels and the longitudinal changes in several serum indicators for oxidative stress. Materials and Methods Seventeen patients on chronic hemodialysis (HD) treatment who had serum UA levels above 8.0  mg/dL and who were not receiving anti-hyperuricemic agents participated in the study. All subjects had oliguria or anuria. The subjects had to be in stable condition, and they had no history of active liver diseases or any other significant medical status, no change in diuretics or steroid therapy within one month of study enrollment and were not chronic users of any nonsteroi- dal anti-inflammatory drugs. The usual medications, such as anti-hypertensive agents, erythropoietin, and phosphate bind- ers, were continued during the study period. Sex was not con- sidered. The exclusion criteria were as follows: age 20 years or 90 years, type I diabetes mellitus or type II diabetes mel- litus with poor glucose control (glycosylated hemoglobin 9% at the start of the observation period), treatment with mercap- topurine hydrate or azathiopurine, pregnancy, and any medi- cal or surgical conditions that made patients unsuitable for this study as judged by the attending physician. All patients were assigned to oral febuxostat and entered the six-month treat- ment period from July through August 2012, during which they initially received febuxostat 10 mg orally once daily in the morning. The target serum UA level was 6.0 mg/dL, and the dose of febuxostat was titrated or increased up to a maximum of 40 mg/day. The blood pressure (BP) was measured before all HD sessions, and the data regarding the systolic BP and diastolic BP were the average of each value on the last HD day of the week. The blood samples were obtained from vascular access, including arteriovenous fistulas and arteriovenous grafts, before HD sessions. The hemoglobin (Hb), hematocrit (Hct), platelet count (Plt), serum levels of UA, blood urea nitrogen (BUN), creatinine (Cr), sodium (Na), chloride (Cl), potas- sium (K), calcium (Ca), inorganic phosphate (Pi), aspartate aminotransferase (AST), alanine aminotransferase (ALT), and lactate dehydrogenase (LDH) were measured at baseline (week 0) and every four weeks during the observation period. The serum levels of 8-hydroxydeoxyguanosine (8-OHdG), 3-nitrotyrosine-modified proteins (3-NT), and protein car- bonyls were determined at baseline and at weeks 4, 12, and 24 during the treatment period. The serum levels of 8-OHdG were measured by an enzyme-linked immunosorbent assay (ELISA) as described previously.10  The ELISA method was also used to measure the serum levels of 3-NT (Japan Institute for the Control of Aging, Nikken SEIL Co, Shizuoka, Japan) and protein carbonyls (BioCell Co, Auckland, New Zealand). This study was performed in accordance with the Declaration of Helsinki and was approved by the medical ethics committee of Jichi Medical University, and all patients included in the present study provided their informed consent. The data were expressed either as the number of partici- pants or as the percentage (%) of the study population. The remaining data were expressed as the means ± standard devia- tion (SD), or as medians and interquartile ranges (IR) for vari- ables with a skewed distribution. A repeated measures analysis of variance combined with Fisher’s protected least significant difference test for normal distributions and the Kruskal– Wallis test with Dunn’s method for skewed distributions were used to compare the time course data, when appropriate. Val- ues of P  0.05 were considered to be statistically significant. The statistical analyses were performed using the SigmaPlot 12 software program for Windows (Systat Software, Inc., San Jose, CA) unless otherwise stated. Results and Discussion The demographic profiles of the 17  patients included in the present study are summarized in Table 1. No subjects had a history of gouty attacks. The patients had been treated with chronic HD for a median of four years. The causes of advanced CKD included diabetic nephropathy, chronic glomerulone- phritis, hypertensive nephrosclerosis, and polycystic kidney disease. All subjects were on the optimum tolerated medical management. Febuxostat lowered the serum UA levels (8.9 ± 1.0 at baseline) significantly from one month after the initia- tion of the treatment (Fig. 1), and the target serum UA level (6.0  mg/dL) was achieved in 12  patients (70.5%) after one month of treatment, compared to 13 (76.4%) and 14 (82.3%) patients after three and six months of treatment, respectively. After six months, 16  subjects were still under the treatment with oral febuxostat (10  mg/day), and there was Table 1. Demographic profiles of the patients at the start of the study. DEMOGRAPHIC CHARACTERISTICS Age (years) 64 ± 10 Sex (male/female) 15/2 HD duration (years) 6.4 ± 5.7 UNDERLYING CAUSES OF CKD, N (%) Diabetic nephropathy 9 (53) Chronic glomerulonephritis 3 (18) hypertensive nephrosclerosis 3 (18) Polycystic kidney disease 2 (12) MEDICATIONS, N (%) Calcium channel antagonist(s) 7 (41) angiotensin-converting-enzyme inhibitor 1 (6) Angiotensin receptor blocker(s) 7 (41) renin inhibitor 1 (6) Other anti-hypertensive agent(s) 4 (24) Loop diuretic(s) 3 (18) http://www.la-press.com http://www.la-press.com/drug-target-insights-journal-j23 Febuxostat and advanced chronic kidney disease patients 41Drug TargeT InsIghTs 2014:8 one subject who was being treated with a reduced dose of 5 mg/day. Also, only two patients were treated with the agent at a dose of above 10 mg/day at that point, one with 20 mg/day and one with 40  mg/day. All doses of febuxostat were well tolerated by the patients with no withdrawals because of side effects or allergic reactions. Although there was a sig- nificant increase in the systolic BP values obtained at five and six months compared to those observed at baseline, no sig- nificant changes in diastolic BP, Hb, Hct, Plt, BUN, or the serum levels of Cr, Na, Cl, K, Ca, Pi, AST, ALT, or LDH were noted during the observation period (Table 2). There were similar trends in the serum levels of protein carbonyls and 3-NT, while the serum 8-OHdG levels measured after six months were significantly lower than those at the base- line (Table 3). No patients experienced symptoms of gouty arthritis, including joint pain, swelling, or redness,2 during the observation period. The treatment of patients with asymptomatic hyperuri- cemia (a serum UA level higher than 8  mg/dL) with urate- lowering agents has been recommended and applied in Japan,7,11 while the appropriate dose of febuxostat among sub- jects with advanced CKD has not yet been established. The current observations suggest that even relatively low doses of febuxostat, which is approved at a dose of 40  to 60  mg/day as the standard dose for the treatment of hyperuricemia with or without gouty arthritis in Japan, may also work effectively among chronic HD patients for reducing the serum UA to a level that has been arbitrarily proposed as a therapeutic target for hyperuricemia.7,11,12 The validity of the indications for urate- lowering agents among overall subjects with asymptomatic After the treatment with oral febuxostat (month(s)) Baseline 1 4 6 8 * * * * * * * * * * * * 10 12 2 3 4 5 6 U A (m g/ dl ) Figure 1. The serum ua levels before and after the initiation of the treatment with oral febuxostat. after six months of febuxostat treatment, the serum UA levels were significantly decreased from those at baseline. all patients were entered into the six-month treatment period from July through august 2012. note that the decrease in the serum ua levels was already significant after one month treatment with febuxostat. Notes: N = 17, **P  0.01 versus baseline. Ta b le 2 . C ha ng es in c lin ic al p ar am et er s du rin g th e ob se rv at io n pe rio d. A F T E R T H E IN IT IA T IO N O F O R A L FE B U X O S TA T T R E A T M E N T P V A LU E B A S E L IN E 1 M O N T H 2 M O N T H S 3 M O N T H S 4 M O N T H S 5 M O N T H S 6 M O N T H S S ys to lic B P (m m H g) 14 1 ± 20 13 7 ± 16 14 1 ± 29 14 1 ± 16 14 2 ± 21 14 8 ± 21 * 14 9 ± 19 *  0. 00 1 D ia st ol ic B P (m m H g) 74 ± 1 1 73 ± 9 73 ± 1 0 76 ± 1 0 76 ± 1 2 74 ± 1 1 73 ± 1 1 0. 18 6 H b (g /d L) 10 .7 ± 1 .0 10 .8 ± 1 .0 10 .9 ± 1 .1 10 .8 ± 1 .6 10 .9 ± 1 .3 10 .9 ± 1 .3 10 .6 ± 1 .0 0. 98 9 H ct ( % ) 33 .9 ± 3 .1 33 .9 ± 3 .2 33 .5 ± 3 .4 34 .1 ± 3 .4 34 .0 ± 4 .3 34 .0 ± 3 .6 33 .1 ± 2 .9 0. 97 6 P lt (× 10 4 / μ l) 16 .8 ( IR : 1 4. 2– 22 .7 ) 15 .6 ( IR : 1 3. 6 –2 5. 1) 17 .8 ( IR : 1 4. 2– 24 .6 ) 18 .4 ( IR : 1 4. 9 –2 5. 2) 17 .7 ( IR : 1 2. 8 –2 3. 1) 16 .7 ( IR : 1 2. 8 –2 1. 6) 18 .3 ( IR : 1 1. 7– 21 .8 ) 0. 88 7 B U N (m g/ dL ) 62 .1 ± 1 1. 7 64 .8 ± 1 8. 6 65 .1 ± 1 5. 8 63 .2 ± 1 4. 1 64 .7 ± 1 9. 1 67 .0 ± 2 1. 4 69 .9 ± 1 6. 5 0. 88 6 C r (m g/ dL ) 11 .4 ± 1 .9 11 .8 ± 2 .0 11 .8 ± 1 .9 11 .8 ± 2 .3 11 .9 ± 2 .2 11 .5 ± 2 .2 11 .5 ± 2 .2 0. 99 1 N a (m m ol /l) 13 8 ± 4 13 9 ± 4 14 0 ± 4 13 9 ± 4 13 9 ± 4 13 9 ± 3 13 8 ± 2 0. 80 5 K (m m ol /l) 4. 9 ± 0. 9 4. 9 ± 0. 8 5. 0 ± 1. 0 5. 0 ± 0. 9 4. 9 ± 0. 7 5. 0 ± 0. 8 5. 0 ± 0. 9 0. 99 9 C l ( m m ol /l) 10 2 ± 5 10 3 ± 4 10 3 ± 4 10 3 ± 4 10 3 ± 5 10 2 ± 4 10 3 ± 3 0. 93 C a (m g/ dL ) 8. 8 ± 0. 8 9. 0 ± 0. 9 8. 8 ± 0. 6 8. 8 ± 0. 6 8. 9 ± 0. 7 9. 1 ± 0. 8 9. 0 ± 0. 9 0. 85 2 P i ( m g/ dL ) 4. 5 ± 1. 3 5. 1 ± 1. 2 5. 3 ± 1. 4 5. 0 ± 0. 9 5. 1 ± 1. 5 5. 6 ± 1. 5 4. 9 ± 1. 0 0. 29 6 A S T ( U /l) 16 .5 ± 1 5. 8 18 .0 ± 1 5. 4 15 .0 ± 6 .7 15 .0 ± 6 .4 17 .2 ± 7 .5 18 .4 ± 8 .4 18 .3 ± 1 3. 6 0. 93 8 A LT ( U /l) 17 .9 ± 1 7. 6 18 .8 ± 1 6. 7 15 .2 ± 9 .4 14 .4 ± 8 .3 14 .0 ± 8 .0 17 .5 ± 1 0. 4 19 .4 ± 1 8. 2 0. 85 7 LD H ( U /l) 17 9 ± 40 18 9 ± 39 17 9 ± 28 17 8 ± 26 18 0 ± 30 19 1 ± 45 18 8 ± 48 0. 92 3 N o te : * P  0 .0 5 ve rs us b as el in e. http://www.la-press.com http://www.la-press.com/drug-target-insights-journal-j23 Akimoto et al 42 Drug TargeT InsIghTs 2014:8 Table 3. The serum levels of several oxidative stress markers before and after the initiation of the treatment with oral febuxostat. AFTER THE INITIATION OF ORAL FEBUXOSTAT TREATMENT P VALUE BASELINE 1 MONTH 3 MONTHS 6 MONTHS Protein carbonyls (nmol/mg protein) 0.07 (IR: 0.03–0.12) 0.10 (IR: 0.06–0.14) 0.07 (IR: 0.06–0.15) 0.05 (IR: 0.03–0.11) 0.329 3-NT (nM) 30.4 (IR: 25.2–40.4) 33.2 (IR: 25.5–42.2) 37.3 (IR: 25.3–45.3) 28.7 (IR: 24.7–43.9) 0.928 8-OHdG (ng/ml) 1.64 (IR: 1.24–2.95) 2.51 (IR: 1.24–4.74) 1.05 (IR: 0.84–1.87) 0.54 (IR: 0.204–1.16)* 0.002 Note: *P  0.05 versus baseline. hyperuricemia remains to be delineated, and clinicians should bear in mind that the prevalence of refractory gout and/or gouty tophi is much lower in Japan in comparison to that in the United States and Europe, where negative opinions regarding pharmaceutical interventions predominate.11–14 One may argue that the clinical benefit of using urate-lowering agents requires careful evaluation, especially in subjects on chronic HD treatment, since an incipient gouty attack is quite rare in hyperuricemic long-term HD patients, and the fre- quency of gouty arthritis has been shown to decrease after the initiation of a periodic HD program in advanced CKD subjects.15,16  Moreover, a significant association between higher serum UA levels and lower mortality, which may be dependent on the favorable nutritional status, has been dem- onstrated in the HD population.17  Otherwise, it may be necessary to focus on the fact that some of the reactive oxy- gen species are produced as a by-product of urate formation through a XO- dependent pathway and the pharmacological nature of febuxostat, which is characterized by a higher bio- availability and a more potent blockade of XO activity than the traditional XO inhibitor allopurinol.1,2,8,18  Indeed, the superior potency of febuxostat to allopurinol for the inhibition of reactive oxygen synthesis has been demonstrated in several reports,19,20 and the serum UA levels could be used as a sur- rogate indicator of the XO activity. In the current study, 8-OHdG, 3-NT, and protein car- bonyls, which have been included in the list of the most com- mon oxidative stress biomarkers in various settings,20,21 were used as the indices of the condition of the present patients. Numerous processes other than the XO-mediated path- way have been implicated in the oxidative stress among the subjects with CKD.21,22  In addition, it has been shown that chronic HD treatment also leads to excessive radical produc- tion and impairment of the anti-oxidant capacity.23  Despite the lack of qualitative information regarding the significance of individual oxidative stress markers,24 we feel that it is rea- sonable to consider that 8-OHdG, but not 3-NT and protein carbonyls, may help to detect the inhibitory effects of febuxo- stat on XO-mediated oxidative stress among the chronic HD patients. Although the precise role of febuxostat in reducing the serum levels of 8-OHdG remains to be delineated, our findings suggest that the generation of 8-OHdG may be more dependent on XO than that of 3-NT or protein carbonyls. On the other hand, it has been proposed that the XO inhibitors may be utilized as adjunctive anti-hypertensive agents in some subsets of hyperuricemic and hypertensive subjects associ- ated with or without advanced CKD,25,26 while we found that the systolic BP levels after five and six months of treatment with febuxostat were higher than those at baseline, despite the titration of anti-hypertensive agents corresponding to the context. We have no explanation for this discrepancy; how- ever, a seasonal bias may have been involved. Indeed, it has been reported that the systolic BP shows seasonal changes in chronic HD patients, with peak BP noted in the winter.27 Finally, the number of patients included in the pres- ent series was quite small, thus implying that this study may be statistically underpowered or that the clinical param- eters may have been overestimated. As such, our findings should be interpreted with caution. Nevertheless, our results encourage us to pursue further investigations regarding the clinical impact of lowering the serum UA level with febux- ostat in chronic HD patients in terms of determining the appropriate dose of the agent as well as concomitantly reduc- ing oxidative stress by blocking XO. Indeed, despite the comparable serum levels of low-density lipoprotein (LDL) between baseline and week 24, we found that the serum lev- els of the oxidative form of LDL, another oxidative stress marker,20 at week 24 were significantly decreased compared to those observed at baseline among the 12 subjects who led us to determine the serum levels of these parameters (data not shown). Obviously, more detailed studies with a larger number of subjects and assessments of the effects of multiple factors affecting hyperuricemia, such as age, sex, and dietary habits,2,14 would shed light on the therapeutic challenges of treating asymptomatic hyperuricemia in patients with vari- ous stages of CKD.28 Author Contributions TA drafted the manuscript. YM, CI, OI, ST, and YW made contributions to the acquisition of the clinical data. EK and DN provided a detailed review of the contents and structure of the manuscript, resulting in significant changes to the origi- nal document. 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