A systematic review of the drug-drug interaction between Statins and Quinolones

Jifang Zhou, Lixia Yu, Huimin Xu
{"title":"A systematic review of the drug-drug interaction between Statins and Quinolones","authors":"Jifang Zhou, Lixia Yu, Huimin Xu","doi":"10.1186/s40360-024-00760-8","DOIUrl":null,"url":null,"abstract":"Statins are widely used in cardiovascular disease (CVD) as a common lipid-lowering drug, while quinolones are widely used for the treatment of infectious diseases. It is common to see CVD in combination with infectious diseases, therefore it is often the case that statins and quinolones are used in combination. Data suggest combinations of statin and quinolone may be associated with potentially life-threatening myopathy, rhabdomyolysis and acute hepatitis. This systematic review aims to characterize data regarding patients affected by the statin-quinolone interaction. The purpose of this systematic review was to collect and evaluate the evidence surrounding statin-quinolone drug interactions and to discuss related risk mitigation strategies. The following databases were searched: PubMed (Medline), Embase, Scopus, and Cochrane Library. The systematic electronic literature search was conducted with the following search terms. In this study, three types of search terms were used: statins-related terms, quinolones-related terms, and drug interactions-related terms. There were 16 case reports that met the criteria for qualitative analysis. Patients were involved in the following adverse reactions: rhabdomyolysis (n = 12), acute hepatitis (n = 1), muscle weakness (n = 1), hip tendinopathy (n = 1), or myopathy (n = 1). In the included literature, patients vary in the dose and type of statins they take, including simvastatin (n = 10) at a dose range of 20–80 mg/d and atorvastatin (n = 4) at a dose of 80 mg/d. There were 2 patients with unspecified statin doses, separately using simvastatin and atorvastatin. The quinolones in combination were ciprofloxacin (n = 9) at a dose range of 800–1500 mg/d, levofloxacin (n = 6) at a dose range of 250–1000 mg/d, and norfloxacin (n = 1) in an unspecified dose range. 81% of the case patients were over 60 years of age, and about 1/3 had kidney-related diseases such as diabetic nephropathy, post-transplantation, and severe glomerulonephritis. Nearly two-third of the patients were on concomitant cytochrome P450 3A4 (CYP3A4) inhibitors, P-glycoprotein (P-gp) inhibitors, or organic anion transporting polypeptide 1B1 (OATP1B1) inhibitors. Patients treated with statin-quinolone combination should be monitored more closely for changes in aspartate aminotransferase or creatine kinase (CK) levels, and muscle symptoms, especially in patients with ciprofloxacin or levofloxacin, with simvastatin and high-dose atorvastatin, over 60 years of age, with kidney-related diseases, and on concomitant CYP3A4 inhibitors.","PeriodicalId":501597,"journal":{"name":"BMC Pharmacology and Toxicology","volume":"24 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"BMC Pharmacology and Toxicology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s40360-024-00760-8","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Statins are widely used in cardiovascular disease (CVD) as a common lipid-lowering drug, while quinolones are widely used for the treatment of infectious diseases. It is common to see CVD in combination with infectious diseases, therefore it is often the case that statins and quinolones are used in combination. Data suggest combinations of statin and quinolone may be associated with potentially life-threatening myopathy, rhabdomyolysis and acute hepatitis. This systematic review aims to characterize data regarding patients affected by the statin-quinolone interaction. The purpose of this systematic review was to collect and evaluate the evidence surrounding statin-quinolone drug interactions and to discuss related risk mitigation strategies. The following databases were searched: PubMed (Medline), Embase, Scopus, and Cochrane Library. The systematic electronic literature search was conducted with the following search terms. In this study, three types of search terms were used: statins-related terms, quinolones-related terms, and drug interactions-related terms. There were 16 case reports that met the criteria for qualitative analysis. Patients were involved in the following adverse reactions: rhabdomyolysis (n = 12), acute hepatitis (n = 1), muscle weakness (n = 1), hip tendinopathy (n = 1), or myopathy (n = 1). In the included literature, patients vary in the dose and type of statins they take, including simvastatin (n = 10) at a dose range of 20–80 mg/d and atorvastatin (n = 4) at a dose of 80 mg/d. There were 2 patients with unspecified statin doses, separately using simvastatin and atorvastatin. The quinolones in combination were ciprofloxacin (n = 9) at a dose range of 800–1500 mg/d, levofloxacin (n = 6) at a dose range of 250–1000 mg/d, and norfloxacin (n = 1) in an unspecified dose range. 81% of the case patients were over 60 years of age, and about 1/3 had kidney-related diseases such as diabetic nephropathy, post-transplantation, and severe glomerulonephritis. Nearly two-third of the patients were on concomitant cytochrome P450 3A4 (CYP3A4) inhibitors, P-glycoprotein (P-gp) inhibitors, or organic anion transporting polypeptide 1B1 (OATP1B1) inhibitors. Patients treated with statin-quinolone combination should be monitored more closely for changes in aspartate aminotransferase or creatine kinase (CK) levels, and muscle symptoms, especially in patients with ciprofloxacin or levofloxacin, with simvastatin and high-dose atorvastatin, over 60 years of age, with kidney-related diseases, and on concomitant CYP3A4 inhibitors.
他汀类药物与喹诺酮类药物相互作用的系统回顾
他汀类药物作为一种常见的降脂药物被广泛用于心血管疾病(CVD),而喹诺酮类药物则被广泛用于治疗感染性疾病。心血管疾病合并感染性疾病的情况很常见,因此他汀类药物和喹诺酮类药物经常被联合使用。有数据表明,他汀类药物和喹诺酮类药物合用可能会导致肌病、横纹肌溶解症和急性肝炎等潜在的生命危险。本系统综述旨在描述受他汀类药物与喹诺酮类药物相互作用影响的患者的相关数据。本系统综述旨在收集和评估他汀类药物与喹诺酮类药物相互作用的相关证据,并讨论相关的风险缓解策略。检索了以下数据库:PubMed(Medline)、Embase、Scopus 和 Cochrane 图书馆。系统性电子文献检索使用了以下检索词。本研究使用了三种检索词:他汀类药物相关词、喹诺酮类药物相关词和药物相互作用相关词。有 16 份病例报告符合定性分析的标准。患者涉及以下不良反应:横纹肌溶解(12 例)、急性肝炎(1 例)、肌无力(1 例)、髋关节肌腱病(1 例)或肌病(1 例)。在收录的文献中,患者服用他汀类药物的剂量和类型各不相同,其中辛伐他汀(10 例)的剂量范围为 20-80 毫克/天,阿托伐他汀(4 例)的剂量为 80 毫克/天。有 2 名患者的他汀类药物剂量不详,分别使用辛伐他汀和阿托伐他汀。联合使用的喹诺酮类药物有环丙沙星(9 例),剂量范围为 800-1500 毫克/天;左氧氟沙星(6 例),剂量范围为 250-1000 毫克/天;诺氟沙星(1 例),剂量范围不详。81%的病例患者年龄超过60岁,约1/3的患者患有与肾脏相关的疾病,如糖尿病肾病、移植后肾病和严重肾小球肾炎。近三分之二的患者同时服用细胞色素 P450 3A4 (CYP3A4) 抑制剂、P-糖蛋白 (P-gp) 抑制剂或有机阴离子转运多肽 1B1 (OATP1B1) 抑制剂。使用他汀-喹诺酮类复方制剂治疗的患者应更密切地监测天冬氨酸氨基转移酶或肌酸激酶(CK)水平的变化以及肌肉症状,尤其是使用环丙沙星或左氧氟沙星、辛伐他汀和大剂量阿托伐他汀、60 岁以上、患有肾脏相关疾病以及同时服用 CYP3A4 抑制剂的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信