Evidence map›Paper›PMID 40596361›Full record

ArticleScientific reports2025

Assessment of drug induced hyperuricemia and gout risk using the FDA adverse event reporting system.

Guihao Zheng, Meifeng Lu, Yulong Ouyang, Shuilin Chen, Bei Hu, Shuai Xu, Guicai Sun

Abstract read
In one paragraph

Article in Scientific reports, 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. Trial
  2. Article
  3. Review
  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

7 authors.

Guihao Zheng *Department of Sports Medicine, Orthopaedic Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwai Zhengjie, Donghu District, Nanchang City, Jiangxi Province, China.
Meifeng Lu *Department of Sports Medicine, Orthopaedic Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwai Zhengjie, Donghu District, Nanchang City, Jiangxi Province, China.
Yulong OuyangDepartment of Sports Medicine, Orthopaedic Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwai Zhengjie, Donghu District, Nanchang City, Jiangxi Province, China.
Shuilin ChenDepartment of Sports Medicine, Orthopaedic Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwai Zhengjie, Donghu District, Nanchang City, Jiangxi Province, China.
Bei HuDepartment of Sports Medicine, Orthopaedic Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwai Zhengjie, Donghu District, Nanchang City, Jiangxi Province, China.
Shuai XuDepartment of Sports Medicine, Orthopaedic Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwai Zhengjie, Donghu District, Nanchang City, Jiangxi Province, China.
Guicai SunDepartment of Sports Medicine, Orthopaedic Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, 17 Yongwai Zhengjie, Donghu District, Nanchang City, Jiangxi Province, China. ndsfy0740@ncu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hyperuricemia, the key pathological basis of gout, is increasingly prevalent worldwide. While lifestyle factors contribute, various medications also play a role. However, their specific risks and mechanisms remain inadequately studied. Disproportionality analysis (ROR, PRR, BCPNN) was used to assess drug-induced hyperuricemia and gout reports (Q1 2004-Q3 2023). Univariate analysis, LASSO, XGBoost, and multivariate regression identified independent risk factors. Time-to-onset analysis evaluated the occurrence timing post-drug initiation. A total of 18,531 reports related to hyperuricemia and gout were identified. Reports involving male patients were significantly more frequent than those involving female patients for both hyperuricemia and gout. The mean ages of patients were relatively high, at 58.7 years (standard deviation [SD] 18.6 years) for hyperuricemia and 64.6 years (SD 13.5 years) for gout. Signal detection identified 131 drugs associated with hyperuricemia and 177 drugs associated with gout. Among the hyperuricemia-related reports, telaprevir was the most frequently implicated drug, whereas lenalidomide ranked highest in the gout-related reports. Subsequent multivariate analysis following machine learning-based screening identified male sex and older age as independent risk factors for drug-induced hyperuricemia and gout. Specifically, peginterferon alfa-2b was found to be an independent risk factor for drug-induced hyperuricemia, while 20 drugs-including pegloticase, febuxostat, allopurinol, rofecoxib, and furosemide-were identified as independent risk factors for drug-induced gout. Furthermore, the median time to onset (TTO) of drug-induced hyperuricemia and gout was 11 days (interquartile range [IQR]: 2-63 days) and 31 days (IQR: 1-269 days), respectively. Notably, over 50% of cases occurred within the first 30 days after initiation of the implicated drug. By leveraging FAERS-based signal detection, this study systematically elucidated significant associations between various drugs and the risks of hyperuricemia and gout. Furthermore, key independent risk factors-including sex, age, and specific drugs-were identified through machine learning and multivariate analysis. These findings provide valuable insights for pharmacovigilance and clinical medication management.

Indexed as

Adverse Drug Reaction Reporting SystemsGoutHyperuricemiaAdultAgedFemaleHumansMaleMiddle AgedRisk FactorsUnited StatesUnited States Food and Drug AdministrationDrug-InducedFAERS databaseGoutHyperuricemiaMultivariate analysisRisk assessmentTime-to-Onset

Identifiers

PMID40596361
PMCPMC12218991

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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.