Department of Clinical Pharmacology and Toxicology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Am J Hypertens. 2013 Sep;26(9):1070-5. doi: 10.1093/ajh/hpt090. Epub 2013 Jun 8.
Ramipril, an inhibitor of the angiotensin-converting enzyme (ACEI), is a drug commonly used in the therapy of hypertension. ACEI-induced hepatotoxicity is rare, and most of the reported cases are associated with captopril. Here, we present the first case of ramipril-induced liver injury proven by positive rechallenge and a review of the literature including the data from the US Food and Drug Administration adverse event reporting system (FAERS).
Patient data were collected in the Berlin Case-Control Surveillance Study for adverse drug reactions. PubMed research on ACEI-induced hepatotoxicity included all ACEIs except captopril; analysis of the FAERS database focused on ramipril-induced hepatotoxicity in the period 2009-2011.
A 40-year-old male patient presented with acute onset jaundice and highly (>20-fold increase of alanine aminotranferase (ALT)) elevated liver enzymes (LEs). Viral or autoimmune hepatitis and biliary etiology were ruled out. Withdrawal of several medications including ramipril resulted in an immediate decrease in LEs, whereas a subsequent re-exposure with ramipril resulted in a striking increase in LEs (>35-fold increase of ALT). After definitely discontinuing ramipril, a rapid decline in LEs was observed, suggesting a certain causal relationship between drug intake and hepatic damage. Analysis of the FAERS database retrieved 65 cases of ramipril-associated hepatotoxicity, with jaundice being the most frequent hepatic adverse event. PubMed research detected 23 relevant publications, with enalapril being the ACEI most commonly reported as being associated with liver injury.
ACEI-induced hepatotoxicity is rare. Our case confirms a hepatotoxic potential of ramipril, highlighting the need for alertness among physicians regarding this matter.
雷米普利是一种血管紧张素转换酶抑制剂(ACEI),是治疗高血压的常用药物。ACEI 引起的肝毒性很少见,大多数报道的病例与卡托普利有关。在这里,我们报告了首例雷米普利引起的肝损伤,该病例通过阳性再激发试验得到证实,并对包括美国食品和药物管理局不良事件报告系统(FAERS)数据在内的文献进行了回顾。
在柏林药物不良反应病例对照监测研究中收集患者数据。对 ACEI 引起的肝毒性的 PubMed 研究包括除卡托普利以外的所有 ACEI;对 FAERS 数据库的分析侧重于 2009-2011 年期间雷米普利引起的肝毒性。
一名 40 岁男性患者出现急性黄疸和高度升高的肝酶(ALT 升高超过 20 倍)。排除了病毒性或自身免疫性肝炎和胆道病因。停用包括雷米普利在内的几种药物后,肝酶立即下降,而随后再次暴露于雷米普利时,肝酶显著升高(ALT 升高超过 35 倍)。停用雷米普利后,肝酶迅速下降,表明药物摄入与肝损伤之间存在一定的因果关系。对 FAERS 数据库的分析检索到 65 例与雷米普利相关的肝毒性病例,其中黄疸是最常见的肝不良事件。PubMed 研究检测到 23 篇相关出版物,其中依那普利是最常报告与肝损伤相关的 ACEI。
ACEI 引起的肝毒性很少见。我们的病例证实了雷米普利具有肝毒性潜力,这突出表明医生对此类问题应保持警惕。