Dexamethasone is a dose-dependent perpetrator of drug-drug interactions: implications for use in people living with HIV

被引:8
|
作者
Jacobs, Tom G. [1 ]
Marzolini, Catia [2 ,3 ,4 ,5 ,6 ,7 ]
Back, David J. [7 ]
Burger, David M. [1 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Radboud Inst Hlth Sci, Dept Pharm, Nijmegen, Netherlands
[2] Univ Hosp Basel, Dept Med, Div Infect Dis, Basel, Switzerland
[3] Univ Hosp Basel, Dept Med, Hosp Epidemiol, Basel, Switzerland
[4] Univ Hosp Basel, Dept Clin Res, Div Infect Dis, Basel, Switzerland
[5] Univ Hosp Basel, Dept Clin Res, Hosp Epidemiol, Basel, Switzerland
[6] Univ Basel, Basel, Switzerland
[7] Univ Liverpool, Dept Mol & Clin Pharmacol, Liverpool, Merseyside, England
关键词
GLUCOCORTICOID-RECEPTOR; HUMAN HEPATOCYTES; GENE-EXPRESSION; X-RECEPTOR; PHARMACOKINETICS; INDUCTION; RIFAPENTINE; INCREASE; THERAPY;
D O I
10.1093/jac/dkab412
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Global use of dexamethasone in COVID-19 patients has revealed a poor understanding of the drug-drug interaction (DDI) potential of dexamethasone, particularly with antiretroviral agents (ARVs). Dexamethasone is both a substrate and a dose-dependent inducer of cytochrome P450 3A4 (CYP3A4). As many ARVs are substrates and/or inhibitors or inducers of CYP3A4, there is concern about DDIs with dexamethasone either as a perpetrator or a victim. Assessment of DDIs that involve dexamethasone is complex as dexamethasone is used at a range of daily doses (generally 0.5 up to 40 mg) and a treatment course can be short, long, or intermittent. Moreover, DDIs with dexamethasone have been evaluated only for a limited number of drugs. Here, we summarize the available in vitro and in vivo data on the interaction potential of dexamethasone and provide recommendations for the management of DDIs with ARVs, considering various dexamethasone dosages and treatment durations.
引用
收藏
页码:568 / 573
页数:6
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