Effect of the Xanthine Oxidase Inhibitor, Febuxostat, on WBC Count in Asymptomatic Hyperuricemia: Subanalysis of the Randomized PRIZE Study

Aims: The anti-inflammatory effects of the xanthine oxidase inhibitor, febuxostat, a urate-lowering agent, have been reported in animal studies. However, the anti-inflammatory effects of urate-lowering therapy and its associated cardiovascular protective effects have not been fully determined in act...

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Veröffentlicht in:Journal of Atherosclerosis and Thrombosis 2024/06/01, Vol.31(6), pp.864-875
Hauptverfasser: Takeshita, Mitsuhide, Tanaka, Atsushi, Yoshida, Hisako, Nakamura, Ikuko, Shibata, Yoshisato, Hata, Shiro, Kushiyama, Akifumi, Okutsu, Masaaki, Ishizu, Tomoko, Node, Koichi
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container_issue 6
container_start_page 864
container_title Journal of Atherosclerosis and Thrombosis
container_volume 31
creator Takeshita, Mitsuhide
Tanaka, Atsushi
Yoshida, Hisako
Nakamura, Ikuko
Shibata, Yoshisato
Hata, Shiro
Kushiyama, Akifumi
Okutsu, Masaaki
Ishizu, Tomoko
Node, Koichi
description Aims: The anti-inflammatory effects of the xanthine oxidase inhibitor, febuxostat, a urate-lowering agent, have been reported in animal studies. However, the anti-inflammatory effects of urate-lowering therapy and its associated cardiovascular protective effects have not been fully determined in actual clinical practice. This study aimed to investigate the effect of febuxostat on white blood cell (WBC) count in patients with asymptomatic hyperuricemia and to assess for potential correlations between changes in WBC count and inflammatory biomarkers and atherosclerosis in this patient population.Methods: This was a post hoc subanalysis of the PRIZE study, a multicenter, prospective, randomized, open-label clinical trial. In the PRIZE study, asymptomatic hyperuricemia patients were randomized to febuxostat group or control group with non-pharmacological therapy and evaluated the effect on vascular. The primary endpoints of this study were the assessment of the time course of WBC count over 24 months and its changes from baseline. Correlations of WBC count with high-sensitivity C-reactive protein (hs-CRP) and mean common carotid artery (CCA)-IMT were also exploratorily examined in the febuxostat group.Results: A total of 444 patients (febuxostat group, n=223; control group, n=221) with WBC measurements available at baseline and at least one of the follow-up time points of 12 or 24 months, were enrolled. Febuxostat modestly, but significantly, reduced WBC counts at 12 and 24 months compared with the baseline levels (P=0.002 and P=0.026, respectively). Notably, the WBC count in the febuxostat group at 12 and 24 months was significantly lower than that in the control group (P=0.007 and P=0.023, respectively). The changes in WBC count were associated with those of hs-CRP (P=0.038), but not with CCA-IMT (P=0.727).Conclusions: Febuxostat therapy for 24 months modestly, but significantly, decreased WBC count in patients with asymptomatic hyperuricemia. This might potentially reflect a modest anti-inflammatory action of febuxostat in clinical settings.
doi_str_mv 10.5551/jat.64574
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However, the anti-inflammatory effects of urate-lowering therapy and its associated cardiovascular protective effects have not been fully determined in actual clinical practice. This study aimed to investigate the effect of febuxostat on white blood cell (WBC) count in patients with asymptomatic hyperuricemia and to assess for potential correlations between changes in WBC count and inflammatory biomarkers and atherosclerosis in this patient population.Methods: This was a post hoc subanalysis of the PRIZE study, a multicenter, prospective, randomized, open-label clinical trial. In the PRIZE study, asymptomatic hyperuricemia patients were randomized to febuxostat group or control group with non-pharmacological therapy and evaluated the effect on vascular. The primary endpoints of this study were the assessment of the time course of WBC count over 24 months and its changes from baseline. Correlations of WBC count with high-sensitivity C-reactive protein (hs-CRP) and mean common carotid artery (CCA)-IMT were also exploratorily examined in the febuxostat group.Results: A total of 444 patients (febuxostat group, n=223; control group, n=221) with WBC measurements available at baseline and at least one of the follow-up time points of 12 or 24 months, were enrolled. Febuxostat modestly, but significantly, reduced WBC counts at 12 and 24 months compared with the baseline levels (P=0.002 and P=0.026, respectively). Notably, the WBC count in the febuxostat group at 12 and 24 months was significantly lower than that in the control group (P=0.007 and P=0.023, respectively). The changes in WBC count were associated with those of hs-CRP (P=0.038), but not with CCA-IMT (P=0.727).Conclusions: Febuxostat therapy for 24 months modestly, but significantly, decreased WBC count in patients with asymptomatic hyperuricemia. This might potentially reflect a modest anti-inflammatory action of febuxostat in clinical settings.</description><identifier>ISSN: 1340-3478</identifier><identifier>ISSN: 1880-3873</identifier><identifier>EISSN: 1880-3873</identifier><identifier>DOI: 10.5551/jat.64574</identifier><identifier>PMID: 38220209</identifier><language>eng</language><publisher>Japan: Japan Atherosclerosis Society</publisher><subject>Aged ; Asymptomatic hyperuricemia ; Biomarkers - blood ; C-Reactive Protein - analysis ; C-Reactive Protein - metabolism ; Febuxostat ; Febuxostat - pharmacology ; Febuxostat - therapeutic use ; Female ; Follow-Up Studies ; Gout Suppressants - therapeutic use ; Humans ; Hyperuricemia - blood ; Hyperuricemia - drug therapy ; Inflammation ; Leukocyte Count ; Male ; Middle Aged ; Original ; Prospective Studies ; Uric Acid - blood ; WBC count ; Xanthine Oxidase - antagonists &amp; inhibitors</subject><ispartof>Journal of Atherosclerosis and Thrombosis, 2024/06/01, Vol.31(6), pp.864-875</ispartof><rights>This article is distributed under the terms of the latest version of CC BY-NC-SA defined by the Creative Commons Attribution License.</rights><rights>2024 Japan Atherosclerosis Society 2024</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c619t-39ed798f93219343dbebaeea709091b09f40c432b0d41110a0338fd65c2322113</citedby><cites>FETCH-LOGICAL-c619t-39ed798f93219343dbebaeea709091b09f40c432b0d41110a0338fd65c2322113</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11150717/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11150717/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,1877,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38220209$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Takeshita, Mitsuhide</creatorcontrib><creatorcontrib>Tanaka, Atsushi</creatorcontrib><creatorcontrib>Yoshida, Hisako</creatorcontrib><creatorcontrib>Nakamura, Ikuko</creatorcontrib><creatorcontrib>Shibata, Yoshisato</creatorcontrib><creatorcontrib>Hata, Shiro</creatorcontrib><creatorcontrib>Kushiyama, Akifumi</creatorcontrib><creatorcontrib>Okutsu, Masaaki</creatorcontrib><creatorcontrib>Ishizu, Tomoko</creatorcontrib><creatorcontrib>Node, Koichi</creatorcontrib><creatorcontrib>Faculty of Medicine</creatorcontrib><creatorcontrib>Department of Medical Statistics</creatorcontrib><creatorcontrib>New Tokyo Hospital</creatorcontrib><creatorcontrib>Sasebo City General Hospital</creatorcontrib><creatorcontrib>Department of Pharmacotherapy</creatorcontrib><creatorcontrib>University of Tsukuba</creatorcontrib><creatorcontrib>Department of Cardiovascular Medicine</creatorcontrib><creatorcontrib>Saga University</creatorcontrib><creatorcontrib>Meiji Pharmaceutical University</creatorcontrib><creatorcontrib>Osaka Metropolitan University Graduate School of Medicine</creatorcontrib><creatorcontrib>Department of Cardiology</creatorcontrib><creatorcontrib>Saga-Ken Medical Centre Koseikan</creatorcontrib><creatorcontrib>Miyazaki Medical Association Hospital</creatorcontrib><title>Effect of the Xanthine Oxidase Inhibitor, Febuxostat, on WBC Count in Asymptomatic Hyperuricemia: Subanalysis of the Randomized PRIZE Study</title><title>Journal of Atherosclerosis and Thrombosis</title><addtitle>JAT</addtitle><description>Aims: The anti-inflammatory effects of the xanthine oxidase inhibitor, febuxostat, a urate-lowering agent, have been reported in animal studies. However, the anti-inflammatory effects of urate-lowering therapy and its associated cardiovascular protective effects have not been fully determined in actual clinical practice. This study aimed to investigate the effect of febuxostat on white blood cell (WBC) count in patients with asymptomatic hyperuricemia and to assess for potential correlations between changes in WBC count and inflammatory biomarkers and atherosclerosis in this patient population.Methods: This was a post hoc subanalysis of the PRIZE study, a multicenter, prospective, randomized, open-label clinical trial. In the PRIZE study, asymptomatic hyperuricemia patients were randomized to febuxostat group or control group with non-pharmacological therapy and evaluated the effect on vascular. The primary endpoints of this study were the assessment of the time course of WBC count over 24 months and its changes from baseline. Correlations of WBC count with high-sensitivity C-reactive protein (hs-CRP) and mean common carotid artery (CCA)-IMT were also exploratorily examined in the febuxostat group.Results: A total of 444 patients (febuxostat group, n=223; control group, n=221) with WBC measurements available at baseline and at least one of the follow-up time points of 12 or 24 months, were enrolled. Febuxostat modestly, but significantly, reduced WBC counts at 12 and 24 months compared with the baseline levels (P=0.002 and P=0.026, respectively). Notably, the WBC count in the febuxostat group at 12 and 24 months was significantly lower than that in the control group (P=0.007 and P=0.023, respectively). The changes in WBC count were associated with those of hs-CRP (P=0.038), but not with CCA-IMT (P=0.727).Conclusions: Febuxostat therapy for 24 months modestly, but significantly, decreased WBC count in patients with asymptomatic hyperuricemia. This might potentially reflect a modest anti-inflammatory action of febuxostat in clinical settings.</description><subject>Aged</subject><subject>Asymptomatic hyperuricemia</subject><subject>Biomarkers - blood</subject><subject>C-Reactive Protein - analysis</subject><subject>C-Reactive Protein - metabolism</subject><subject>Febuxostat</subject><subject>Febuxostat - pharmacology</subject><subject>Febuxostat - therapeutic use</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gout Suppressants - therapeutic use</subject><subject>Humans</subject><subject>Hyperuricemia - blood</subject><subject>Hyperuricemia - drug therapy</subject><subject>Inflammation</subject><subject>Leukocyte Count</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Original</subject><subject>Prospective Studies</subject><subject>Uric Acid - blood</subject><subject>WBC count</subject><subject>Xanthine Oxidase - antagonists &amp; inhibitors</subject><issn>1340-3478</issn><issn>1880-3873</issn><issn>1880-3873</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkttuEzEQhlcIREvhghdAvgSpKT7ugZuqRGkbqVJRCwJxY3m9s42jXTvY3irbV-ClcZI2wM3MSPPrn_F8zrK3BJ8IIcjHpYonORcFf5YdkrLEE1YW7HmqGU81L8qD7FUIS4wZE4K-zA5YSSmmuDrMfs_aFnRErkVxAeiHsnFhLKDrtWlUADS3C1Ob6PwxOod6WLsQVTxGzqLvn6do6gYbkbHoLIz9KrpeRaPR5bgCP3ijoTfqE7odamVVNwYTnsbcKNu43jxAg77czH_O0G0cmvF19qJVXYA3j_ko-3Y--zq9nFxdX8ynZ1cTnZMqTlgFTVGVbcUoqRhnTQ21AlAFrnBFaly1HGvOaI0bTgjBKj27bJtcaMooJYQdZac739VQ99BosNGrTq686ZUfpVNG_t-xZiHv3L1MbgIXpEgO7x8dvPs1QIiyN0FD1ykLbgiSVoRTwUglkvTDTqq9C8FDu59DsNzQk4me3NJL2nf_LrZXPuFKgoudIHWNVp2zXYIll27w6cJBwrpIdx2VTHIuE2-C85RSWeabUAi--Rpc_L3BMgG9g_0o5RPBDrZLMSLzbdgst-_ohfISLPsDomPDvw</recordid><startdate>20240601</startdate><enddate>20240601</enddate><creator>Takeshita, Mitsuhide</creator><creator>Tanaka, Atsushi</creator><creator>Yoshida, Hisako</creator><creator>Nakamura, Ikuko</creator><creator>Shibata, Yoshisato</creator><creator>Hata, Shiro</creator><creator>Kushiyama, Akifumi</creator><creator>Okutsu, Masaaki</creator><creator>Ishizu, Tomoko</creator><creator>Node, Koichi</creator><general>Japan Atherosclerosis Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240601</creationdate><title>Effect of the Xanthine Oxidase Inhibitor, Febuxostat, on WBC Count in Asymptomatic Hyperuricemia: Subanalysis of the Randomized PRIZE Study</title><author>Takeshita, Mitsuhide ; Tanaka, Atsushi ; Yoshida, Hisako ; Nakamura, Ikuko ; Shibata, Yoshisato ; Hata, Shiro ; Kushiyama, Akifumi ; Okutsu, Masaaki ; Ishizu, Tomoko ; Node, Koichi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c619t-39ed798f93219343dbebaeea709091b09f40c432b0d41110a0338fd65c2322113</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Aged</topic><topic>Asymptomatic hyperuricemia</topic><topic>Biomarkers - blood</topic><topic>C-Reactive Protein - analysis</topic><topic>C-Reactive Protein - metabolism</topic><topic>Febuxostat</topic><topic>Febuxostat - pharmacology</topic><topic>Febuxostat - therapeutic use</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gout Suppressants - therapeutic use</topic><topic>Humans</topic><topic>Hyperuricemia - blood</topic><topic>Hyperuricemia - drug therapy</topic><topic>Inflammation</topic><topic>Leukocyte Count</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Original</topic><topic>Prospective Studies</topic><topic>Uric Acid - blood</topic><topic>WBC count</topic><topic>Xanthine Oxidase - antagonists &amp; inhibitors</topic><toplevel>online_resources</toplevel><creatorcontrib>Takeshita, Mitsuhide</creatorcontrib><creatorcontrib>Tanaka, Atsushi</creatorcontrib><creatorcontrib>Yoshida, Hisako</creatorcontrib><creatorcontrib>Nakamura, Ikuko</creatorcontrib><creatorcontrib>Shibata, Yoshisato</creatorcontrib><creatorcontrib>Hata, Shiro</creatorcontrib><creatorcontrib>Kushiyama, Akifumi</creatorcontrib><creatorcontrib>Okutsu, Masaaki</creatorcontrib><creatorcontrib>Ishizu, Tomoko</creatorcontrib><creatorcontrib>Node, Koichi</creatorcontrib><creatorcontrib>Faculty of Medicine</creatorcontrib><creatorcontrib>Department of Medical Statistics</creatorcontrib><creatorcontrib>New Tokyo Hospital</creatorcontrib><creatorcontrib>Sasebo City General Hospital</creatorcontrib><creatorcontrib>Department of Pharmacotherapy</creatorcontrib><creatorcontrib>University of Tsukuba</creatorcontrib><creatorcontrib>Department of Cardiovascular Medicine</creatorcontrib><creatorcontrib>Saga University</creatorcontrib><creatorcontrib>Meiji Pharmaceutical University</creatorcontrib><creatorcontrib>Osaka Metropolitan University Graduate School of Medicine</creatorcontrib><creatorcontrib>Department of Cardiology</creatorcontrib><creatorcontrib>Saga-Ken Medical Centre Koseikan</creatorcontrib><creatorcontrib>Miyazaki Medical Association Hospital</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Takeshita, Mitsuhide</au><au>Tanaka, Atsushi</au><au>Yoshida, Hisako</au><au>Nakamura, Ikuko</au><au>Shibata, Yoshisato</au><au>Hata, Shiro</au><au>Kushiyama, Akifumi</au><au>Okutsu, Masaaki</au><au>Ishizu, Tomoko</au><au>Node, Koichi</au><aucorp>Faculty of Medicine</aucorp><aucorp>Department of Medical Statistics</aucorp><aucorp>New Tokyo Hospital</aucorp><aucorp>Sasebo City General Hospital</aucorp><aucorp>Department of Pharmacotherapy</aucorp><aucorp>University of Tsukuba</aucorp><aucorp>Department of Cardiovascular Medicine</aucorp><aucorp>Saga University</aucorp><aucorp>Meiji Pharmaceutical University</aucorp><aucorp>Osaka Metropolitan University Graduate School of Medicine</aucorp><aucorp>Department of Cardiology</aucorp><aucorp>Saga-Ken Medical Centre Koseikan</aucorp><aucorp>Miyazaki Medical Association Hospital</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of the Xanthine Oxidase Inhibitor, Febuxostat, on WBC Count in Asymptomatic Hyperuricemia: Subanalysis of the Randomized PRIZE Study</atitle><jtitle>Journal of Atherosclerosis and Thrombosis</jtitle><addtitle>JAT</addtitle><date>2024-06-01</date><risdate>2024</risdate><volume>31</volume><issue>6</issue><spage>864</spage><epage>875</epage><pages>864-875</pages><artnum>64574</artnum><issn>1340-3478</issn><issn>1880-3873</issn><eissn>1880-3873</eissn><abstract>Aims: The anti-inflammatory effects of the xanthine oxidase inhibitor, febuxostat, a urate-lowering agent, have been reported in animal studies. However, the anti-inflammatory effects of urate-lowering therapy and its associated cardiovascular protective effects have not been fully determined in actual clinical practice. This study aimed to investigate the effect of febuxostat on white blood cell (WBC) count in patients with asymptomatic hyperuricemia and to assess for potential correlations between changes in WBC count and inflammatory biomarkers and atherosclerosis in this patient population.Methods: This was a post hoc subanalysis of the PRIZE study, a multicenter, prospective, randomized, open-label clinical trial. In the PRIZE study, asymptomatic hyperuricemia patients were randomized to febuxostat group or control group with non-pharmacological therapy and evaluated the effect on vascular. The primary endpoints of this study were the assessment of the time course of WBC count over 24 months and its changes from baseline. Correlations of WBC count with high-sensitivity C-reactive protein (hs-CRP) and mean common carotid artery (CCA)-IMT were also exploratorily examined in the febuxostat group.Results: A total of 444 patients (febuxostat group, n=223; control group, n=221) with WBC measurements available at baseline and at least one of the follow-up time points of 12 or 24 months, were enrolled. Febuxostat modestly, but significantly, reduced WBC counts at 12 and 24 months compared with the baseline levels (P=0.002 and P=0.026, respectively). Notably, the WBC count in the febuxostat group at 12 and 24 months was significantly lower than that in the control group (P=0.007 and P=0.023, respectively). The changes in WBC count were associated with those of hs-CRP (P=0.038), but not with CCA-IMT (P=0.727).Conclusions: Febuxostat therapy for 24 months modestly, but significantly, decreased WBC count in patients with asymptomatic hyperuricemia. This might potentially reflect a modest anti-inflammatory action of febuxostat in clinical settings.</abstract><cop>Japan</cop><pub>Japan Atherosclerosis Society</pub><pmid>38220209</pmid><doi>10.5551/jat.64574</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record>
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subjects Aged
Asymptomatic hyperuricemia
Biomarkers - blood
C-Reactive Protein - analysis
C-Reactive Protein - metabolism
Febuxostat
Febuxostat - pharmacology
Febuxostat - therapeutic use
Female
Follow-Up Studies
Gout Suppressants - therapeutic use
Humans
Hyperuricemia - blood
Hyperuricemia - drug therapy
Inflammation
Leukocyte Count
Male
Middle Aged
Original
Prospective Studies
Uric Acid - blood
WBC count
Xanthine Oxidase - antagonists & inhibitors
title Effect of the Xanthine Oxidase Inhibitor, Febuxostat, on WBC Count in Asymptomatic Hyperuricemia: Subanalysis of the Randomized PRIZE Study
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