Losartan: A Pharmacotherapy in Cardiovascular Disease

Z. Tolou_Ghamari
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Abstract

A recently published article confirmed that in 2019, around 523 million people suffered from cardiovascular disease (including 18.6 million deaths) worldwide. Losartan, a drug, was patented 35 years ago and approved for medical use in the United States in 1995 (28 years ago). As an effective treatment for hypertension, losartan blocks the interaction of angiotensin II with its receptor by inhibiting the renin-angiotensin system. This article aims to review the available literature and recent studies demonstrating the efficacy, safety, mechanism of action and drug-drug interactions of losartan in cardiovascular disease. This is a focused literature review with the keywords relevant to the terms performed in PubMed, Scopus and Web of Science through May 28, 2023, according to the PRISMA guidelines. Based on the PICO standard format, fifty-two relevant in-depth consequent guide approaches and evidence-based choices were selected associated with a knowledgeable collection of current, high-quality manuscripts. After oral administration, time to reach maximum concentration is about 1-2 hours. With a 78% binding to protein, it has a bioavailability of 25-35%. Losartan is not removed by hemodialysis. For the full effect to occur, it may take up to 6 weeks. The drug is mainly prescribed for patients with high blood pressure, diabetic nephropathy, hypertension and left ventricular hypertrophy. The publication reported higher drug exposures and adverse reactions in women than men with antihypertensive medications. Losartan could improve changes in gut microbiota that might be associated with hypertension. In the high-risk group of renal transplant recipients with arterial hypertension, research reported well-controlled blood pressure with losartan monotherapy. In addition to the major losartan interactions with captopril, enalapril, lisinopril, and lithium, there are moderate interactions with aspirin, pregabalin, alprazolam, amitriptyline, baclofen, betamethasone, buspirone. Muscle cramps, respiratory infection, cough, hyperkalemia, anemia and stuffy nose are the main reported side effects. As polypharmacy could hide pharmacokinetics interaction due to cytochrome P450, therefore, the combination of losartan with drugs such as phenobarbital, rifampin or fluconazole needs vigilant attention regarding therapeutic drug monitoring.
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氯沙坦:心血管疾病的药物治疗
最近发表的一篇文章证实,2019年,全球约有5.23亿人患有心血管疾病(包括1860万人死亡)。氯沙坦是一种药物,35年前获得专利,1995年(28年前)在美国获准用于医疗用途。氯沙坦通过抑制肾素-血管紧张素系统阻断血管紧张素II与其受体的相互作用,是治疗高血压的有效药物。本文旨在综述氯沙坦治疗心血管疾病的有效性、安全性、作用机制和药物-药物相互作用的现有文献和最新研究。根据PRISMA指南,这是一篇重点文献综述,其中的关键词与PubMed、Scopus和Web of Science中截止到2023年5月28日的相关术语相关。基于PICO标准格式,选择了52个相关的深入后续指导方法和基于证据的选择,并与当前高质量手稿的知识集合相关联。口服后,达到最大浓度的时间约为1-2小时。与蛋白质的结合率为78%,生物利用度为25-35%。氯沙坦不能通过血液透析去除。要达到完全效果,可能需要长达6周的时间。该药主要用于高血压、糖尿病肾病、高血压、左室肥厚患者。该出版物报道了服用降压药的女性比男性有更高的药物暴露和不良反应。氯沙坦可以改善可能与高血压有关的肠道微生物群的变化。在动脉性高血压肾移植受者的高危人群中,研究报告氯沙坦单药治疗血压控制良好。氯沙坦除了与卡托普利、依那普利、赖诺普利和锂的主要相互作用外,还与阿司匹林、普瑞巴林、阿普唑仑、阿米替林、巴氯芬、倍他米松、丁螺环酮有中度相互作用。肌肉痉挛、呼吸道感染、咳嗽、高钾血症、贫血和鼻塞是报道的主要副作用。多药联用可隐藏细胞色素P450引起的药代动力学相互作用,因此氯沙坦与苯巴比妥、利福平、氟康唑等药物联用治疗药物监测需引起高度重视。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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