Evidence map›Paper›PMID 36534221›Full record

Trial reportInternational urology and nephrology2023

Effects of febuxostat on delaying chronic kidney disease progression: a randomized trial in China.

Hongtao Yang, Rong Li, Qing Li, Tiekun Yan, Yuefeng Li, Qun Huang, Shunya Uchida, Wenxiu Chang

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in International urology and nephrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 6 pooled it
4.3field-weighted citation impact, top 4% 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

8 citing papers in PubMed, 6 syntheses or guidelines pooled it, 24 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Guideline
  4. Pooled it
  5. Pooled it
  6. Pooled it
  7. Article
  8. Review
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

8 authors at 8 institutions in 2 countries.

Hongtao Yang *Department of Nephrology, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Rong LiDepartment of Nephrology, Second Hospital of Tianjin Medical University, Tianjin, China.
Qing LiDepartment of Nephrology, Taida International Cardiovascular Hospital, Tianjin, China.
Tiekun YanDepartment of Nephrology, Tianjin Medical University General Hospital, Tianjin, China.
Yuefeng LiDepartment of Nephrology, Tianjin Haihe Hospital, Tianjin, China.
Qun HuangDepartment of Nephrology, Tianjin Haibin People's Hospital, Tianjin, China.
Shunya UchidaDepartment of Medicine, Teikyo University School of Medicine, Tokyo, Japan.
Wenxiu Chang *Department of Nephrology, Tianjin First Center Hospital, No. 24 Fukang Road, Nankai District, Tianjin, 300192, China. changwx@sina.com.ORCID http://orcid.org/0000-0001-6269-5694
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine · CNSecond Hospital of Tianjin Medical University · CNTEDA International Cardiovascular Hospital · CNTeikyo Heisei University · JPTianjin First Center Hospital · CNTianjin haihe hospital · CNTianjin Medical University General Hospital · CNTianjin People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA few studies have tested febuxostat for its usefulness in delaying chronic kidney disease (CKD) progression by treating hyperuricemia and results were controversial. Thus, we attempted to conduct a randomized controlled study using the Chinese population with advanced grade of CKD.

methodsOne hundred CKD patients in stages 3 and 4 with asymptomatic hyperuricemia from seven medical centers were included in this prospective randomized controlled study and assigned to the control and febuxostat group, the latter of which received febuxostat to titrate to achieve serum uric acid (SUA) < 6 mg/dL. The observation period was 12 months. The primary outcomes included the event of estimated glomerular filtration rate (eGFR) decline ≥ 30% or 50% from baseline at 12 months, dialysis and death from CKD; secondary outcome was the change in eGFR. Safety analysis was also performed.

resultsForty-seven patients and 45 patients in the febuxostat and control groups, respectively completed the study. Seven of 47 (14.9%) participants reached 30% decline in eGFR in the febuxostat group, while 1 (2.1%) and 2 (4.3%) patients reached 50% decline in eGFR or dialysis. Thirteen (28.9%), 10 (22.2%) and 3 (6.7%) of 45 patients reached primary kidney outcomes separately in the control group. The change in eGFR after 12 months from baseline in the febuxostat group was 0.50 mL/min/1.73 m

conclusionsFebuxostat effectively slowed eGFR decline in patients with CKD stages 3 and 4 and asymptomatic hyperuricemia.

Indexed as

HyperuricemiaRenal Insufficiency, ChronicDisease ProgressionFebuxostatGout SuppressantsHumansProspective StudiesTreatment OutcomeUric AcidFebuxostatGout SuppressantsUric AcidChronic kidney diseaseEstimated glomerular filtration rateFebuxostatHyperuricemia

Identifiers

PMID36534221
OpenAlexW4311931244

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.