包括抗精神病药物和抗高血压药物的药物相互作用

IF 3.9 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
C. A. Buzea, L. Dima, C. Correll, P. Manu
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引用次数: 3

摘要

摘要引言抗精神病药物是治疗被诊断为主要精神障碍患者的主要药物。在代谢综合征的其他组成部分中,高血压是这些患者的常见症状。由于他们的精神和身体发病率,许多患者接受多种药物治疗,使他们面临临床相关药物相互作用的风险。涵盖的领域本综述总结了抗精神病药物和用于治疗高血压的主要药物类别之间已知或潜在的药物-药物相互作用的知识。我们的目的是让临床医生深入了解这些药物之间的药代动力学和药效学相互作用,以便更好地选择药物组合来治疗精神疾病和心血管风险因素。为此,我们在PubMed和Scopus数据库中进行了文献检索,截至2021年7月31日。专家意见抗精神病药物和抗高血压药物之间的主要药代动力学相互作用主要涉及细胞色素P450系统。药效相互作用是由多种机制产生的,导致同时与同一受体结合。关于药物相互作用的现有数据主要基于病例报告和小型研究,因此应谨慎解读。目前的知识足够强大,可以指导临床医生选择更安全的药物组合,如下所述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Drug–drug interactions involving antipsychotics and antihypertensives
ABSTRACT Introduction Antipsychotics represent the mainstay in the treatment of patients diagnosed with major psychiatric disorders. Hypertension, among other components of metabolic syndrome, is a common finding in these patients. For their psychiatric and physical morbidity, many patients receive polypharmacy, exposing them to the risk of clinically relevant drug–drug interactions. Areas covered This review summarizes the knowledge regarding the known or potential drug–drug interactions between antipsychotics and the main drug classes used in the treatment of hypertension. We aimed to provide the clinician an insight into the pharmacokinetic and pharmacodynamic interactions between these drugs for a better choice of combinations of drugs to treat both the mental illness and cardiovascular risk factors. For this, we performed a literature search in PubMed and Scopus databases, up to 31 July 2021. Expert opinion The main pharmacokinetic interactions between antipsychotics and antihypertensive drugs involve mainly the cytochrome P450 system. The pharmacodynamic interactions are produced by multiple mechanisms, leading to concurrent binding to the same receptors. The data available regarding drug–drug interactions is mostly based on case reports and small studies and therefore should be interpreted with caution. The current knowledge is sufficiently strong to guide clinicians in selecting safer drug combinations as summarized here.
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来源期刊
Expert Opinion on Drug Metabolism & Toxicology
Expert Opinion on Drug Metabolism & Toxicology 医学-生化与分子生物学
CiteScore
7.90
自引率
2.30%
发文量
62
审稿时长
4-8 weeks
期刊介绍: Expert Opinion on Drug Metabolism & Toxicology (ISSN 1742-5255 [print], 1744-7607 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles on all aspects of ADME-Tox. Each article is structured to incorporate the author’s own expert opinion on the scope for future development. The Editors welcome: Reviews covering metabolic, pharmacokinetic and toxicological issues relating to specific drugs, drug-drug interactions, drug classes or their use in specific populations; issues relating to enzymes involved in the metabolism, disposition and excretion of drugs; techniques involved in the study of drug metabolism and toxicology; novel technologies for obtaining ADME-Tox data. Drug Evaluations reviewing the clinical, toxicological and pharmacokinetic data on a particular drug. The audience consists of scientists and managers in the pharmaceutical industry, pharmacologists, clinical toxicologists and related professionals.
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