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使用美国食品药品监督管理局不良事件报告系统评估药物性高尿酸血症和痛风风险。

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

作者信息

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

机构信息

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.

Graduate School of Jiangxi Medical College, Nanchang University, Nanchang city, Jiangxi Province, China.

出版信息

Sci Rep. 2025 Jul 2;15(1):22856. doi: 10.1038/s41598-025-06114-6.

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.

摘要

高尿酸血症是痛风的关键病理基础,在全球范围内日益普遍。虽然生活方式因素有影响,但各种药物也起作用。然而,它们的具体风险和机制仍研究不足。采用不成比例分析(风险比、报告比值比、贝叶斯置信度神经网络)评估药物性高尿酸血症和痛风报告(2004年第一季度至2023年第三季度)。单因素分析、套索回归、极端梯度提升和多因素回归确定了独立危险因素。发病时间分析评估了用药后发病的时间。共识别出18531份与高尿酸血症和痛风相关的报告。高尿酸血症和痛风的报告中,涉及男性患者的明显多于涉及女性患者的。患者的平均年龄相对较高,高尿酸血症患者为58.7岁(标准差[SD]18.6岁),痛风患者为64.6岁(SD 13.5岁)。信号检测识别出131种与高尿酸血症相关的药物和177种与痛风相关的药物。在与高尿酸血症相关的报告中,特拉匹韦是最常涉及的药物,而来那度胺在与痛风相关的报告中排名最高。基于机器学习筛选后的后续多因素分析确定男性和老年是药物性高尿酸血症和痛风的独立危险因素。具体而言,聚乙二醇干扰素α-2b被发现是药物性高尿酸血症的独立危险因素,而包括聚乙二醇尿酸酶、非布司他、别嘌醇、罗非昔布和呋塞米在内的20种药物被确定为药物性痛风的独立危险因素。此外,药物性高尿酸血症和痛风的中位发病时间(TTO)分别为11天(四分位间距[IQR]:2-63天)和31天(IQR:1-269天)。值得注意的是,超过50%的病例发生在使用相关药物后的前30天内。通过利用基于美国食品药品监督管理局不良事件报告系统的信号检测,本研究系统地阐明了各种药物与高尿酸血症和痛风风险之间的显著关联。此外,通过机器学习和多因素分析确定了关键的独立危险因素,包括性别、年龄和特定药物。这些发现为药物警戒和临床用药管理提供了有价值的见解。

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