Evidence map›Paper›PMID 38220209›Full record

Trial reportJournal of atherosclerosis and thrombosis2024

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

Mitsuhide Takeshita, Atsushi Tanaka, Hisako Yoshida, Ikuko Nakamura, Yoshisato Shibata, Shiro Hata, Akifumi Kushiyama, Masaaki Okutsu, Tomoko Ishizu, Koichi Node

Abstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Journal of atherosclerosis and thrombosis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Gout, Uric Acid, and Coronary Artery Disease.Journal of atherosclerosis and thrombosis · 2025
    Review
  2. Leucocyte Count: Inflammatory and ROS Biomarkers of ASCVD.Journal of atherosclerosis and thrombosis · 2024
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Mitsuhide TakeshitaDepartment of Cardiovascular Medicine, Saga University.
Atsushi TanakaDepartment of Cardiovascular Medicine, Saga University.
Hisako YoshidaDepartment of Medical Statistics, Osaka Metropolitan University Graduate School of Medicine.
Ikuko NakamuraDepartment of Cardiovascular Medicine, Saga-Ken Medical Centre Koseikan.
Yoshisato ShibataDepartment of Cardiology, Miyazaki Medical Association Hospital.
Shiro HataDepartment of Cardiology, Sasebo City General Hospital.
Akifumi KushiyamaDepartment of Pharmacotherapy, Meiji Pharmaceutical University.
Masaaki OkutsuDepartment of Cardiovascular Medicine, New Tokyo Hospital.
Tomoko IshizuDepartment of Cardiology, Faculty of Medicine, University of Tsukuba.
Koichi NodeDepartment of Cardiovascular Medicine, Saga University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsThe 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.

methodsThis 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.

resultsA 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).

conclusionsFebuxostat 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.

Indexed as

FebuxostatHyperuricemiaXanthine OxidaseAgedBiomarkersC-Reactive ProteinFemaleFollow-Up StudiesGout SuppressantsHumansLeukocyte CountMaleMiddle AgedProspective StudiesUric AcidBiomarkersC-Reactive ProteinFebuxostatGout SuppressantsUric AcidXanthine OxidaseAsymptomatic hyperuricemiaFebuxostatInflammationWBC count

Identifiers

PMID38220209
PMCPMC11150717

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.