药物-药物相互作用包括抗精神病药物与降糖药、降脂药和减肥药的联合作用。

IF 3.9 3区 医学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Expert Opinion on Drug Metabolism & Toxicology Pub Date : 2022-11-01 DOI:10.1080/17425255.2022.2147425
Catalin Adrian Buzea, Peter Manu, Lorena Dima, Christoph U Correll
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引用次数: 1

摘要

重度精神疾病(SMI)患者患糖尿病、血脂异常和其他代谢综合征的风险很高。患有这些代谢合并症和心脏危险因素的患者不仅应该接受抗精神病药物治疗,还应该接受旨在降低心血管风险的药物治疗。因此,许多患者可能暴露于临床相关的药物-药物相互作用。涵盖领域:本叙述性综述总结了抗精神病药物和治疗代谢综合征成分的药物之间已知或潜在的药物-药物相互作用的数据,但高血压除外,高血压已在其他地方总结。在PubMed和Scopus中检索截至2021年7月31日的有关抗精神病药物与用于治疗代谢综合征成分的药物之间相互作用的文献,旨在告知临床医生对需要药物干预的重度精神障碍患者和心脏代谢危险因素的药物选择。专家意见:细胞色素P450系统和p糖蛋白转运体(在较小程度上)参与抗精神病药物与某些他汀类药物或沙格列汀之间的药代动力学相互作用。关于药效学相互作用,现有信息主要基于小型研究,对于较新的药物类别,如PCSK9抑制剂或SGLT2抑制剂,数据仍然缺乏。然而,有足够的信息来指导临床医生选择更安全的抗精神病-心脏代谢风险降低药物组合。
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Drug-drug interactions involving combinations of antipsychotic agents with antidiabetic, lipid-lowering, and weight loss drugs.

Introduction: Patients with severe mental illness (SMI) have a high risk for diabetes, dyslipidemia, and other components of metabolic syndrome. Patients with these metabolic comorbidities and cardiac risk factors should receive not only antipsychotics but also medications aiming to reduce cardiovascular risk. Therefore, many patients may be exposed to clinically relevant drug-drug interactions.

Areas covered: This narrative review summarizes data regarding the known or potential drug-drug interactions between antipsychotics and medications treating metabolic syndrome components, except for hypertension, which has been summarized elsewhere. A literature search in PubMed and Scopus up to 7/31/2021 was performed regarding interactions between antipsychotics and drugs used to treat metabolic syndrome components, aiming to inform clinicians' choice of medication for patients with SMI and cardiometabolic risk factors in need of pharmacologic interventions.

Expert opinion: The cytochrome P450 system and, to a lesser extent, the P-glycoprotein transporter is involved in the pharmacokinetic interactions between antipsychotics and some statins or saxagliptin. Regarding pharmacodynamic interactions, the available information is based mostly on small studies, and for newer classes, like PCSK9 inhibitors or SGLT2 inhibitors, data are still lacking. However, there is sufficient information to guide clinicians in the process of selecting safer antipsychotic-cardiometabolic risk reduction drug combinations.

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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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