Zhang Sha, Yan Ming-Ming, Zhao Hui, Qiu Xiao-Yan, Zhu Deqiu
Department of Pharmacy, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Department of Pharmacy, Huashan Hospital, Fudan University, Shanghai, China.
Front Pharmacol. 2024 Sep 16;15:1445324. doi: 10.3389/fphar.2024.1445324. eCollection 2024.
Currently, there remains substantial controversy in research regarding whether the concomitant use of colchicine and statins increases the occurrence of rhabdomyolysis, warranting further substantiation.
This study aimed to identify the likelihood drug-drug interactions (DDIs) for the co-administration of colchicine and statins resulting in rhabdomyolysis.
A disproportionality analysis was conducted by using data sourced from the US Food and Drug Administration Adverse Event Reporting System (FAERS) to detect rhabdomyolysis signals associated with the combined use of colchicine and statins. The association between (colchicine/statins/colchicine and statins) and rhabdomyolysis were evaluated using information component (IC). DDI signals were calculated based on the Ω shrinkage measure and Bayesian confidence propagation neural network (BCPNN) method. Furthermore, stratification was performed based on colchicine and individual statins agents.
In total, 11,119 reports of rhabdomyolysis were identified in the FAERS database, 255 (2.29%) involved both colchicine and statins. Our analysis showed potential DDI signals of rhabdomyolysis (Ω = 1.17) among individuals concurrent use of colchicine and statins. Moreover, further drug-specific analysis suggests DDI signals in the colchicine-atorvastatin pair (Ω = 1.12), and colchicine-rosuvastatin pair (Ω = 1.05), along with a higher proportion of rhabdomyolysis (IC = 5.20) and (IC = 4.26), respectively.
The findings suggest that concomitant use of colchicine and statins may increase the risk of rhabdomyolysis, particularly when combined with atorvastatin or rosuvastatin. Therefore, healthcare professionals should pay special attention to life-threatening AE such as rhabdomyolysis, when co-prescribing colchicine statins.
目前,关于秋水仙碱与他汀类药物联合使用是否会增加横纹肌溶解症的发生率,在研究中仍存在大量争议,需要进一步证实。
本研究旨在确定秋水仙碱与他汀类药物联合使用导致横纹肌溶解症的药物相互作用(DDI)可能性。
通过使用来源于美国食品药品监督管理局不良事件报告系统(FAERS)的数据进行不成比例分析,以检测与秋水仙碱和他汀类药物联合使用相关的横纹肌溶解症信号。使用信息成分(IC)评估(秋水仙碱/他汀类药物/秋水仙碱和他汀类药物)与横纹肌溶解症之间的关联。基于Ω收缩测量和贝叶斯置信传播神经网络(BCPNN)方法计算DDI信号。此外,根据秋水仙碱和个别他汀类药物进行分层。
在FAERS数据库中总共识别出11119例横纹肌溶解症报告,其中255例(2.29%)同时涉及秋水仙碱和他汀类药物。我们的分析显示,在同时使用秋水仙碱和他汀类药物的个体中存在横纹肌溶解症的潜在DDI信号(Ω = 1.17)。此外,进一步的药物特异性分析表明,秋水仙碱与阿托伐他汀组合(Ω = 1.12)以及秋水仙碱与瑞舒伐他汀组合(Ω = 1.05)存在DDI信号,且横纹肌溶解症的比例分别更高(IC = 5.20)和(IC = 4.26)。
研究结果表明,秋水仙碱与他汀类药物联合使用可能会增加横纹肌溶解症的风险,特别是与阿托伐他汀或瑞舒伐他汀联合使用时。因此,医疗保健专业人员在联合开具秋水仙碱和他汀类药物时,应特别注意如横纹肌溶解症等危及生命的不良事件。