Weiss-Tessbach Matthias, Dizdarevic Al Medina, Kupis Alexander, Bischof Thorsten, Firbas Christa, Quehenberger Peter, Derhaschnig Ulla, Frimmel Max, Jilma Bernd, Schoergenhofer Christian
Department of Clinical Pharmacology, Medical University of Vienna, Vienna, Vienna, Austria.
Department of Laboratory Medicine, Medical University of Vienna, Vienna, Vienna, Austria.
Front Pharmacol. 2025 May 12;16:1579014. doi: 10.3389/fphar.2025.1579014. eCollection 2025.
Laxatives are among the most commonly used pharmacological agents worldwide. Available data indicate a significant potential for clinically relevant drug-drug interactions. We hypothesized that osmotic laxatives may reduce the oral bioavailability of the direct oral anticoagulant dabigatran and thereby its anticoagulant effects.
In the first part of this single-centre, randomized, double-blind, crossover trial, 24 healthy volunteers received 150 mg dabigatran with placebo (10 g glucose) or 20 g lactulose. In the second, open label part, eight of these 24 healthy volunteers were randomly assigned to receive dabigatran with either 27.6 g macrogol, 30 g flaxseeds, or to receive 20 g lactulose 4-h after dabigatran intake. We measured dabigatran plasma concentrations using an ecarin-based chromogenic assay and calculated the pharmacokinetic parameters. Statistical analysis was performed using a linear mixed-effects model on log-transformed AUC values.
The main pharmacokinetic parameters AUC, C, T, or t did not differ significantly between most treatment periods. A reduction in AUC was observed with flaxseed compared to placebo. Dabigatran's pharmacokinetics remained unaffected by concomitant intake of lactulose or macrogol. There was a high inter- and intra-individual variability in the pharmacokinetics of dabigatran.
In this study osmotic laxatives such as lactulose, macrogol or flaxseeds did not affect the pharmacokinetics of dabigatran in healthy individuals. These findings support the safe concurrent use of dabigatran with osmotic laxatives.
泻药是全球最常用的药物之一。现有数据表明,临床上药物相互作用的可能性很大。我们推测,渗透性泻药可能会降低直接口服抗凝剂达比加群的口服生物利用度,从而降低其抗凝效果。
在这项单中心、随机、双盲、交叉试验的第一部分,24名健康志愿者服用150毫克达比加群,同时服用安慰剂(10克葡萄糖)或20克乳果糖。在第二部分开放标签试验中,这24名健康志愿者中的8人被随机分配,分别在服用达比加群后服用27.6克聚乙二醇、30克亚麻籽,或在服用达比加群4小时后服用20克乳果糖。我们使用基于蛇毒凝血酶的显色测定法测量达比加群的血浆浓度,并计算药代动力学参数。使用线性混合效应模型对对数转换后的AUC值进行统计分析。
大多数治疗期间的主要药代动力学参数AUC、C、T或t差异不显著。与安慰剂相比,亚麻籽组的AUC有所降低。达比加群的药代动力学不受同时服用乳果糖或聚乙二醇的影响。达比加群的药代动力学在个体间和个体内存在很大差异。
在本研究中,乳果糖、聚乙二醇或亚麻籽等渗透性泻药对健康个体的达比加群药代动力学没有影响。这些发现支持达比加群与渗透性泻药同时安全使用。