Evidence map›Paper›PMID 42277723›Full record

SynthesisBMC nephrology2026

Efficacy and safety of low-dose combination urate-lowering agent therapy versus standard-dose monotherapy in patients with hyperuricemia and/or gout: a systematic review and meta-analysis of randomized controlled trials.

Takashi Sakaguchi, Hisatomi Arima, Makoto Okada, Taichi Maruyama, Ayako Goto, Kazutoshi Ito, Reimi Tsurusawa, Tamami Ueno, Kazumi Kawano, Makiko Abe and 5 more

Abstract readSystematic ReviewMeta-AnalysisComparative Study
In one paragraph

Synthesis in BMC nephrology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Takashi SakaguchiDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan. tsakaguchi@fukuoka-u.ac.jp.
Hisatomi ArimaDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Makoto OkadaDepartment of Pediatrics, Fukuoka University Chikushi Hospital, Fukuoka, Japan.
Taichi MaruyamaTsunagaru Family Clinic, Fukuoka, Japan.
Ayako GotoDepartment of Pediatrics, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, Japan.
Kazutoshi ItoDepartment of Pediatrics, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, Japan.
Reimi TsurusawaDepartment of Pediatrics, The Kouhou-kai Takagi Hospital, Okawa, Japan.
Tamami UenoDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Kazumi KawanoDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Makiko AbeDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Toshiki MaedaDepartment of Preventive Medicine and Public Health, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Kosuke MasutaniDivision of Nephrology and Rheumatology, Department of Internal Medicine, Faculty of Medicine, Fukuoka University, Fukuoka, Japan.
Chikara YoshimuraCenter of Sleep Medicine, Fukuoka University Hospital, Fukuoka, Japan.
Shunsuke FunakoshiDepartment of Medical Laboratory Science, Faculty of Health Science, Junshin Gakuen University, Fukuoka, Japan.
Shinichiro NagamitsuDepartment of Pediatrics, Faculty of Medicine, Fukuoka University, 7-45-1 Nanakuma, Jonan-ku, Fukuoka, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTreatment to lower uric acid levels is usually administered using monotherapy. However, this may be insufficiently effective for all patients. We hypothesized that a low-dose combination of drugs with different mechanisms of action might be more effective than standard-dose monotherapy. To test this theory, we conducted a systematic review and meta-analysis.

methodWe searched MEDLINE and the Cochrane Library to identify randomized controlled trials that compared combination therapy involving low-dose urate-lowering drugs with standard-dose monotherapy. The primary outcome was serum uric acid levels at the end of treatment, and the data were analyzed using a random-effects model. Adverse events were assessed qualitatively.

resultsThis review included four trials involving 342 participants. Statistically significant reductions in serum uric acid levels were observed with low-dose combination therapy compared to monotherapy (mean difference: -0.47 mg/dL; 95% confidence interval: -0.68 to -0.26). No statistically significant heterogeneity was observed (I² = 0.0%). No serious adverse events were reported in either group.

conclusionsThe results suggest that low-dose combination therapy with urate production inhibitors and urate excretion promoters may be more effective at lowering serum uric acid levels compared with standard-dose monotherapy. However, as the assessment of adverse events was qualitative and the certainty of the safety evidence was extremely low, it remains unclear whether there are differences in the safety profiles between treatment strategies. Further randomized controlled trials are needed to confirm these findings.

Indexed as

GoutGout SuppressantsHyperuricemiaUric AcidDose-Response Relationship, DrugDrug Therapy, CombinationHumansRandomized Controlled Trials as TopicTreatment OutcomeGout SuppressantsUric AcidLow-dose combination therapyMeta-analysisRandomized controlled trialsSystematic reviewUrate-lowering therapy

Identifiers

PMID42277723
PMCPMC13488130

What OpenQuestion holds

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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.