Xu Min, Xu Shanggang, Yi Xueliang
Department of Respiratory, Clinical Medical College & Affliated Hospital of Chengdu University, Chengdu University, Chengdu, 610036, China.
Department of Emergency, Clinical Medical College & Affliated Hospital of Chengdu University, Chengdu University, Chengdu, 610036, China.
BMC Immunol. 2025 May 2;26(1):35. doi: 10.1186/s12865-025-00714-7.
This study utilizes the FDA Adverse Event Reporting System (FAERS) database to compare the adverse reaction signals of cyclosporine and tacrolimus, two widely used immunosuppressants, in relation to drug-induced kidney injury. The findings aim to inform clinical decision-making.
The study retrospectively analyzed data from January 2004 to September 2024, employing both frequency analysis and Bayesian methods. We assessed and compared the mortality rates, hospitalization rates, and the association of cyclosporine and tacrolimus with kidney injury to elucidate the renal toxicity of these two drugs.
After data processing, we identified a total of 3,449 cyclosporine-related kidney injury reports and 5,538 tacrolimus-related kidney injury reports. The results revealed a stronger association between tacrolimus and kidney injury. Additionally, kidney injuries associated with both cyclosporine and tacrolimus predominantly affected males. Furthermore, the hospitalization rate for cyclosporine-related kidney injury was 34.40%, compared to 44.50% for tacrolimus. The mortality rate associated with cyclosporine-induced kidney injury was higher than that of tacrolimus.
This study utilized the FDA Adverse Event Reporting System (FAERS) database from January 2004 to September 2024 to perform a comprehensive analysis of adverse drug-related kidney injury reactions to cyclosporine and tacrolimus. The results suggest that both cyclosporine and tacrolimus are associated with renal injury, but tacrolimus appears to reduce mortality while increasing hospitalization rates. This serves as a critical warning for planning future treatment regimens, drug monitoring, and reducing adverse effects.
本研究利用美国食品药品监督管理局不良事件报告系统(FAERS)数据库,比较两种广泛使用的免疫抑制剂环孢素和他克莫司与药物性肾损伤相关的不良反应信号。研究结果旨在为临床决策提供依据。
本研究回顾性分析了2004年1月至2024年9月的数据,采用频率分析和贝叶斯方法。我们评估并比较了死亡率、住院率以及环孢素和他克莫司与肾损伤的关联,以阐明这两种药物的肾毒性。
经过数据处理,我们共识别出3449例与环孢素相关的肾损伤报告和5538例与他克莫司相关的肾损伤报告。结果显示他克莫司与肾损伤之间的关联更强。此外,与环孢素和他克莫司相关的肾损伤主要影响男性。此外,环孢素相关肾损伤的住院率为34.40%,而他克莫司为44.50%。环孢素所致肾损伤的死亡率高于他克莫司。
本研究利用2004年1月至2024年9月的FDA不良事件报告系统(FAERS)数据库,对环孢素和他克莫司与药物相关的肾损伤不良反应进行了全面分析。结果表明,环孢素和他克莫司均与肾损伤有关,但他克莫司似乎在降低死亡率的同时增加了住院率。这为规划未来治疗方案、药物监测和减少不良反应提供了重要警示。