Evidence map›Paper›PMID 38530491›Full record

Trial reportClinical and experimental nephrology2024

Multicenter randomized controlled trial of intensive uric acid lowering therapy for CKD patients with hyperuricemia: TARGET-UA.

Tetsuya Yamamoto, Masato Kasahara, Kenji Ueshima, Shiro Uemura, Naoki Kashihara, Kenjiro Kimura, Tsuneo Konta, Tetsuo Shoji, Akira Mima, Masashi Mukoyama and 1 more

Abstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Clinical and experimental nephrology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. SGLT2 Inhibitors and Uric Acid Homeostasis.Gout, urate, and crystal deposition disease · 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

11 authors.

Tetsuya YamamotoGyoumeikan Hospital, Osaka, Japan.
Masato KasaharaNara Medical University, Kashihara, Japan. kasa@naramed-u.ac.jp.ORCID http://orcid.org/0000-0002-1833-9075
Kenji UeshimaUjitakeda Hospital, Uji, Japan.
Shiro UemuraKawasaki Medical School, Okayama, Japan.
Naoki KashiharaKawasaki Medical School, Okayama, Japan.
Kenjiro KimuraJCHO Tokyo Takanawa Hospital, Tokyo, Japan.
Tsuneo KontaYamagata University, Yamagata, Japan.
Tetsuo ShojiOsaka Metropolitan University, Osaka, Japan.
Akira MimaOsaka Medical and Pharmaceutical University, Osaka, Japan.
Masashi MukoyamaKumamoto University, Kumamoto, Japan.
Yoshihiko SaitoNara Medical University, Kashihara, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe investigate whether Intensive uric acid (UA)-lowering therapy (ULT) provides increased renal protection compared with standard therapy in chronic kidney disease (CKD) patients.

methodsThis was a multicenter randomized controlled trial. Only CKD patients with hyperuricemia were included in this study. The participants were randomly assigned to either the Intensive therapy group (target serum UA level ≥ 4.0 mg/dL and < 5.0 mg/dL) or the standard therapy group (serum UA level ≥ 6.0 mg/dL and < 7.0 mg/dL). ULT was performed using topiroxostat, a non-purine-type selective xanthine oxidase inhibitor. The primary endpoint was change in the logarithmic value of urine albumin to the creatinine ratio (ACR) between baseline and week 52 of the treatment.

resultsThree hundred fifty-two patients were included in the full analysis set. In the Standard therapy group, mean serum UA was 8.23 mg/dL at baseline and 6.13 mg/dL at 52 weeks. In the Intensive therapy group, mean serum UA was 8.15 mg/dL at baseline and 5.25 mg/dL at 52 weeks. There was no significant difference in changes in log ACR at 52 weeks between the Intensive therapy and the Standard therapy groups.

conclusionThis study did not reveal the benefit of Intensive ULT to improve albuminuria levels. (UMIN000026741 and jRCTs051180146).

Indexed as

AlbuminuriaHyperuricemiaRenal Insufficiency, ChronicUric AcidAgedBiomarkersCreatinineFemaleHumansMaleMiddle AgedNitrilesPyridinesTreatment OutcomeXanthine OxidaseBiomarkersCreatinineFYX-051NitrilesPyridinesUric AcidXanthine OxidaseChronic kidney disease (CKD)Renal functionTopiroxostatUric acid-lowering therapyUrine albumin to the creatinine ratio

Identifiers

PMID38530491
PMCPMC11266370

What Socratic 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 Socratic graph.