Evidence map›Paper›PMID 39932882›Full record

Trial reportRheumatology (Oxford, England)2025

Impact of adding urine alkalization therapy to xanthine oxidase inhibitor in gout management: a prospective cohort study.

Can Wang, Kai Guo, Nicola Dalbeth, Mingshu Sun, Jie Lu, Ying Chen, Hui Zhang, Xuefeng Wang, Xiaopeng Ji, Xinde Li and 8 more

Abstract readClinical Trial
In one paragraph

Trial report in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

18 authors.

Can WangShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.ORCID 0000-0003-0719-3952
Kai GuoShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Nicola DalbethDepartment of Medicine, University of Auckland, Auckland, New Zealand.ORCID 0000-0003-4632-4476
Mingshu SunDepartment of Rheumatology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Jie LuShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.ORCID 0000-0003-2886-8285
Ying ChenDepartment of Endocrinology, The Affiliated Hospital of Qingdao University, Qingdao, China.
Hui ZhangInstitute of Metabolic Diseases, Qingdao University, Qingdao, China.
Xuefeng WangShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Xiaopeng JiShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Xinde LiShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Wenyan SunShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Lin HanShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Lingling CuiShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Zhen LiuShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Aichang JiShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Yuwei HeShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.
Robert TerkeltaubDivision of Rheumatology, Autoimmunity and Inflammation, Department of Medicine, University of California San Diego, La Jolla, CA, USA.
Changgui LiShandong Provincial Key Laboratory of Metabolic Diseases and Qingdao Key Laboratory of Gout, The Affiliated Hospital of Qingdao University, Qingdao, China.ORCID 0000-0002-4622-3731

Funding

National Key Research and Development Program of China 2022YFC2503300National Key Research and Development Program of China 2022YFE0107600National Natural Science Foundation of China 82301003NSFC 82220108015Projects of International Cooperation and ExchangesShandong Provincial Key Research and Development Plan Major Scientific and Technological Innovation 2021CXGC011103
6 · The paper itself

Abstract

objectivesGout patients frequently have decreased urine pH, related to metabolic syndrome (MetS) and chronic kidney disease. Here, we aimed to investigate whether the addition of urine alkalization to urate-lowering therapy (ULT) is associated with improvements in albuminuria, gout flares or MetS outcomes in men with gout and low urinary pH (pH < 6.2).

methodsA prospective cohort study enrolled 385 participants starting ULT with febuxostat (initially 20 mg daily, escalated to 40 mg daily if serum urate ≥360 µmol/l), with or without alkalization based on patient preference using a 3.5 g bid citrate mixture. Participants were followed every 4 weeks to week 12. The primary outcome was urine albumin-to-creatinine ratio (UACR) at week 12.

resultsIn total, 343 participants completed the week 12 visit (137 alkalization, 206 controls). At week 12, compared with controls, participants receiving alkalization required a significantly lower febuxostat dose (by ∼20%) but had no significant difference in serum urate at target <360 µmol/l. Urine pH increased significantly in the alkalization group from week 4 (P < 0.001). At week 12, the alkalization group had a significantly lower UACR compared with control (P < 0.001), without significantly different eGFR. Participants in the alkalization group experienced fewer gout flares and had lower pain visual analogue scale scores (P < 0.001). There were lower serum triglyceride levels (P < 0.01) and higher HDL-C levels (P < 0.001) in the alkalization group. No other differences in metabolic outcomes were observed.

conclusionUrine alkalization was associated with lower UACR, fewer gout flares, and improved serum lipid profile in febuxostat-treated men with gout and low urine pH.

trial registrationChiCTR, http://www.chictr.org.cn, ChiCTR2100043573.

Indexed as

Enzyme InhibitorsFebuxostatGoutGout SuppressantsXanthine OxidaseAgedAlbuminuriaFemaleHumansHydrogen-Ion ConcentrationMaleMetabolic SyndromeMiddle AgedProspective StudiesTreatment OutcomeUric AcidEnzyme InhibitorsFebuxostatGout SuppressantsUric AcidXanthine Oxidasegoutgout flareslipid profiletophiUACRurine alkalization

Identifiers

PMID39932882
PMCPMC12107057

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.