Evidence map›Paper›PMID 35260678›Full record

Trial reportScientific reports2022

Urate-lowering therapy for CKD patients with asymptomatic hyperuricemia without proteinuria elucidated by attribute-based research in the FEATHER Study.

Hiroshi Kataoka, Toshio Mochizuki, Mamiko Ohara, Yuki Tsuruta, Naomi Iwasa, Rie Yoshida, Ken Tsuchiya, Kosaku Nitta, Kenjiro Kimura, Tatsuo Hosoya and 1 more

Open access · goldAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.2field-weighted citation impact, top 2% of its field
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

26 citing papers in PubMed, 44 citations in OpenAlex.

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  18. Efficacy of dotinurad in patients with severe renal dysfunction.Clinical and experimental nephrology · 2024
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  20. Observational
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

11 authors at 20 institutions in 1 country.

Hiroshi KataokaDepartment of Nephrology, Tokyo Women's Medical University, Tokyo, 162-8666, Japan. kataoka@twmu.ac.jp.
Toshio MochizukiDepartment of Nephrology, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
Mamiko OharaDepartment of Nephrology, Kameda Medical Center, Chiba, 296-8602, Japan.
Yuki TsurutaDepartment of Nephrology, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
Naomi IwasaDepartment of Nephrology, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
Rie YoshidaDepartment of Nephrology, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
Ken TsuchiyaDepartment of Blood Purification, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
Kosaku NittaDepartment of Nephrology, Tokyo Women's Medical University, Tokyo, 162-8666, Japan.
Kenjiro KimuraTokyo Takanawa Hospital, Tokyo, 108-8606, Japan.
Tatsuo HosoyaDivision of Chronic Kidney Disease Therapeutics, The Jikei University, Tokyo, Japan.
FEATHER Investigators
Tokyo Women's Medical University · JPJikei University School of Medicine · JPSt. Marianna University School of Medicine · JPHyogo Medical University · JPTeikyo University Hospital · JPChiba East Hospital · JPChugoku Central Hospital · JPEhime Prefectural Central Hospital · JPFujisawa City Hospital · JPHyogo Prefectural Amagasaki General Medical Center · JPJichi Medical University · JPKagawa University Hospital · JPKanazawa University · JPKatsushika Medical Center · JPKawamura Hospital · JPKonan Kosei Hospital · JPNagoya University Hospital · JPNTT Medical Center · JPOkayama University · JPOsaka City University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Attribute-based medicine is essential for patient-centered medicine. To date, the groups of patients with chronic kidney disease (CKD) requiring urate-lowering therapy are clinically unknown. Herein, we evaluated the efficacy of febuxostat using a cross-classification, attribute-based research approach. We performed post hoc analysis of multicenter, randomized, double-blind, placebo-controlled trial data for 395 patients with stage 3 CKD and asymptomatic hyperuricemia. Participants were divided into febuxostat or placebo groups and subcohorts stratified and cross-classified by proteinuria and serum creatinine concentrations. In patients stratified based on proteinuria, the mean eGFR slopes were significantly higher in the febuxostat group than in the placebo group (P = 0.007) in the subcohort without proteinuria. The interaction between febuxostat treatment and presence of proteinuria in terms of eGFR slope was significant (P for interaction = 0.019). When cross-classified by the presence of proteinuria and serum creatinine level, the mean eGFR slopes significantly differed between the febuxostat and placebo groups (P = 0.040) in cross-classified subcohorts without proteinuria and with serum creatinine level ≥ median, but not in the cross-classified subcohorts with proteinuria and serum creatinine level < median. Febuxostat mitigated the decline in kidney function among stage 3 CKD patients with asymptomatic hyperuricemia without proteinuria.

Indexed as

HyperuricemiaRenal Insufficiency, ChronicCreatinineFebuxostatFemaleGout SuppressantsHumansMaleProteinuriaTreatment OutcomeUric AcidCreatinineFebuxostatGout SuppressantsUric Acid

Identifiers

PMID35260678
PMCPMC8904814
OpenAlexW4221123541

What OpenQuestion holds

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LicenceCC BY
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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.