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辛伐他汀对健康受试者中达比加群药代动力学及抗凝作用的影响

Effects of Simvastatin on Pharmacokinetics and Anticoagulant Effects of Dabigatran in Healthy Subjects.

作者信息

Chung Hyewon, Kim Jong-Min, Park Jin-Woo, Noh Jihyeon, Kim Kyoung-Ah, Park Ji-Young

机构信息

Department of Clinical Pharmacology and Toxicology, Guro Hospital, Korea University College of Medicine, Seoul 08308, Republic of Korea.

Department of Clinical Pharmacology and Toxicology, Anam Hospital, Korea University College of Medicine, Seoul 02841, Republic of Korea.

出版信息

Pharmaceuticals (Basel). 2023 Feb 27;16(3):364. doi: 10.3390/ph16030364.

Abstract

Higher risk of major hemorrhage associated with concomitant use of dabigatran and simvastatin compared to other statins was previously reported with a suggestion of P-glycoprotein-mediated interaction. The aim of this study was to evaluate the effects of simvastatin on pharmacokinetics and anticoagulant effects of dabigatran, a direct oral anticoagulant. A total of 12 healthy subjects were enrolled in an open-label, two-period, single sequence study. Subjects were given 150 mg of dabigatran etexilate followed by 40 mg of once-daily simvastatin for seven days. Dabigatran etexilate was administered with simvastatin on the seventh day of simvastatin administration. Blood samples for pharmacokinetic and pharmacodynamic analyses were obtained until 24 h post-dose of dabigatran etexilate with or without co-administration of simvastatin. Pharmacokinetic parameters were derived from noncompartmental analysis for dabigatran etexilate, dabigatran, and dabigatran acylglucuronide. When simvastatin was co-administered, geometric mean ratios of area under time-concentration curves for dabigatran etexilate, dabigatran, and dabigatran acylglucuronide were 1.47, 1.21, and 1.57, respectively, compared to when dabigatran etexilate was administered alone. Thrombin generation assay and coagulation assay showed similar profiles between before and after co-administration of simvastatin. This study provides evidence that simvastatin treatment plays a minor role in modulating pharmacokinetics and anticoagulant effects of dabigatran etexilate.

摘要

先前有报道称,与其他他汀类药物相比,达比加群与辛伐他汀联用会增加大出血风险,提示存在P-糖蛋白介导的相互作用。本研究旨在评估辛伐他汀对直接口服抗凝药达比加群的药代动力学和抗凝效果的影响。共有12名健康受试者参加了一项开放标签、两期、单序列研究。受试者先服用150 mg达比加群酯,随后每天服用40 mg辛伐他汀,共7天。在服用辛伐他汀的第7天,达比加群酯与辛伐他汀同时给药。在达比加群酯给药后24小时内,无论是否联用辛伐他汀,均采集血样进行药代动力学和药效学分析。药代动力学参数通过对达比加群酯、达比加群和达比加群酰基葡萄糖醛酸进行非房室分析得出。与单独服用达比加群酯相比,联用辛伐他汀时,达比加群酯、达比加群和达比加群酰基葡萄糖醛酸的时间-浓度曲线下面积的几何平均比值分别为1.47、1.21和1.57。凝血酶生成试验和凝血试验显示,联用辛伐他汀前后的结果相似。本研究提供了证据,表明辛伐他汀治疗在调节达比加群酯的药代动力学和抗凝效果方面作用较小。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5c9/10056008/5d2e593e80b6/pharmaceuticals-16-00364-g001.jpg

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