Antoniou Tony, Macdonald Erin M, Yao Zhan, Hollands Simon, Gomes Tara, Tadrous Mina, Mamdani Muhammad M, Juurlink David N
Department of Family and Community Medicine (Antoniou), St. Michael's Hospital and University of Toronto; Li Ka Shing Knowledge Institute (Gomes) and Li Ka Shing Centre for Healthcare Analytics Research and Training (Mamdani), St. Michael's Hospital; Leslie Dan Faculty of Pharmacy (Gomes, Tadrous, Mamdani) and Department of Medicine (Juurlink), University of Toronto; Institute for Clinical Evaluative Sciences (Antoniou, Macdonald, Yao, Hollands, Gomes, Tadrous, Mamdani, Juurlink); Applied Health Research Centre (Tadrous), St. Michael's Hospital; Sunnybrook Research Institute (Juurlink), Toronto, Ont.
CMAJ. 2017 Jan 9;189(1):E4-E10. doi: 10.1503/cmaj.160303. Epub 2016 Nov 21.
Dabigatran etexilate is a prodrug whose absorption is opposed by intestinal P-glycoprotein and which is converted by carboxylesterase to its active form, dabigatran. Unlike other statins, simvastatin and lovastatin are potent inhibitors of P-glycoprotein and carboxylesterase, and might either increase the risk of hemorrhage with dabigatran etexilate or decrease its effectiveness.
We conducted 2 population-based, nested case-control studies involving Ontario residents 66 years of age and older who started dabigatran etexilate between May 1, 2012, and Mar. 31, 2014. In the first study, cases were patients with ischemic stroke; in the second, cases were patients with major hemorrhage. Each case was matched with up to 4 controls by age and sex. All cases and controls received a single statin in the 60 days preceding the index date. We determined the association between each outcome and the use of simvastatin or lovastatin, relative to other statins.
Among 45 991 patients taking dabigatran etexilate, we identified 397 cases with ischemic stroke and 1117 cases with major hemorrhage. After multivariable adjustment, use of simvastatin or lovastatin was not associated with an increased risk of stroke (adjusted odds ratio [OR] 1.33, 95% confidence interval [CI] 0.88 to 2.01). In contrast, use of simvastatin and lovastatin were associated with a higher risk of major hemorrhage (adjusted OR 1.46, 95% CI 1.17 to 1.82).
In patients receiving dabigatran etexilate, simvastatin and lovastatin were associated with a higher risk of major hemorrhage relative to other statins. Preferential use of the other statins should be considered in these patients.
达比加群酯是一种前体药物,其吸收受到肠道P-糖蛋白的抑制,并通过羧酸酯酶转化为其活性形式达比加群。与其他他汀类药物不同,辛伐他汀和洛伐他汀是P-糖蛋白和羧酸酯酶的强效抑制剂,可能会增加达比加群酯的出血风险或降低其疗效。
我们进行了两项基于人群的巢式病例对照研究,研究对象为2012年5月1日至2014年3月31日期间开始服用达比加群酯的66岁及以上安大略省居民。在第一项研究中,病例为缺血性中风患者;在第二项研究中,病例为大出血患者。每个病例按年龄和性别与最多4名对照进行匹配。所有病例和对照在索引日期前60天内均服用了单一他汀类药物。我们确定了每种结局与辛伐他汀或洛伐他汀使用之间的关联,并与其他他汀类药物进行了比较。
在45991名服用达比加群酯的患者中,我们确定了397例缺血性中风病例和1117例大出血病例。经过多变量调整后,使用辛伐他汀或洛伐他汀与中风风险增加无关(调整后的优势比[OR]为1.33,95%置信区间[CI]为0.88至2.01)。相比之下,使用辛伐他汀和洛伐他汀与大出血风险较高相关(调整后的OR为1.46,95%CI为1.17至1.82)。
在接受达比加群酯治疗的患者中,相对于其他他汀类药物,辛伐他汀和洛伐他汀与大出血风险较高相关。在这些患者中应考虑优先使用其他他汀类药物。