Cressman Alex M, Macdonald Erin M, Fernandes Kimberly A, Gomes Tara, Paterson J Michael, Mamdani Muhammad M, Juurlink David N
The Institute for Clinical Evaluative Sciences, Toronto, Ontario.
Department of Medicine, Faculty of Medicine, University of Toronto, Ontario.
Br J Clin Pharmacol. 2015 Oct;80(4):662-9. doi: 10.1111/bcp.12682. Epub 2015 Jul 2.
Clopidogrel and angiotensin converting enzyme (ACE) inhibitors are commonly co-prescribed drugs. Clopidogrel inhibits carboxylesterase 1 (CES1), the enzyme responsible for converting prodrug ACE inhibitors (such as ramipril and perindopril) to their active metabolites. The clinical implications of this potential drug interaction are unknown. The clinical consequences of the potential drug interaction between clopidogrel and prodrug ACE inhibitors were examined.
We conducted a nested case-control study of Ontarians aged 66 years and older treated with clopidogrel between September 1 2003 and March 31 2013 following acute myocardial infarction. Cases were subjects who died or were hospitalized for reinfarction or heart failure in the subsequent year, and each was matched with up to four controls. The primary outcome was a composite of reinfarction, heart failure or death. The primary analysis examined whether use of the prodrug ACE inhibitors ramipril or perindopril was more common among cases than use of lisinopril, an active ACE inhibitor.
Among 45 918 patients treated with clopidogrel following myocardial infarction, we identified 4203 cases and 14 964 controls. After adjustment, we found no association between the composite outcome and use of perindopril (adjusted odds ratio (aOR) 0.94, 95% confidence interval (CI) 0.76, 1.16) or ramipril (aOR 0.97, 95% CI 0.80, 1.18), relative to lisinopril. Secondary analyses of each element of the composite outcome yielded similar findings.
Following myocardial infarction, use of clopidogrel with ACE inhibitors activated by CES1 is not associated with an increased risk of adverse cardiovascular outcomes relative to lisinopril. These findings suggest that the recently described drug interaction between clopidogrel and prodrug ACE inhibitors is of little clinical relevance.
氯吡格雷和血管紧张素转换酶(ACE)抑制剂是常用的联合处方药物。氯吡格雷可抑制羧酸酯酶1(CES1),该酶负责将前体药物ACE抑制剂(如雷米普利和培哚普利)转化为其活性代谢产物。这种潜在药物相互作用的临床意义尚不清楚。本研究对氯吡格雷与前体药物ACE抑制剂之间潜在药物相互作用的临床后果进行了研究。
我们对2003年9月1日至2013年3月31日期间因急性心肌梗死接受氯吡格雷治疗的66岁及以上安大略省居民进行了一项巢式病例对照研究。病例为随后一年中死亡、因再梗死或心力衰竭住院的患者,每个病例最多匹配4名对照。主要结局是再梗死、心力衰竭或死亡的复合结局。主要分析考察了与活性ACE抑制剂赖诺普利相比,前体药物ACE抑制剂雷米普利或培哚普利在病例中的使用是否更常见。
在45918例心肌梗死后接受氯吡格雷治疗的患者中,我们确定了4203例病例和14964例对照。调整后,我们发现与赖诺普利相比,复合结局与培哚普利的使用(调整后的优势比(aOR)为0.94,95%置信区间(CI)为0.76,1.16)或雷米普利的使用(aOR为0.97,95%CI为0.80,1.18)之间无关联。对复合结局各要素的次要分析得出了类似的结果。
心肌梗死后,与赖诺普利相比,氯吡格雷与由CES1激活的ACE抑制剂联合使用不会增加不良心血管结局的风险。这些发现表明,最近描述的氯吡格雷与前体药物ACE抑制剂之间的药物相互作用几乎没有临床相关性。