Brown Nancy J, Byiers Stuart, Carr David, Maldonado Mario, Warner Barbara Ann
Division of Clinical Pharmacology, Vanderbilt University School of Medicine, Nashville, TN 37232-6602, USA.
Hypertension. 2009 Sep;54(3):516-23. doi: 10.1161/HYPERTENSIONAHA.109.134197. Epub 2009 Jul 6.
Dipeptidyl peptidase-IV (DPP-IV) inhibitors decrease degradation of the incretins. DPP-IV inhibitors also decrease degradation of peptides, such as substance P, that may be involved in the pathogenesis of angiotensin-converting enzyme (ACE) inhibitor-associated angioedema. This study tested the hypothesis that DPP-IV inhibition affects risk of clinical angioedema, by comparing the incidence of angioedema in patients treated with the DPP-IV inhibitor vildagliptin versus those treated with comparator in Phase III randomized clinical trials. Prospectively defined angioedema-related events were adjudicated in a blinded fashion by an internal medicine adjudication committee and expert reviewer. Concurrent ACE inhibitor or angiotensin receptor blocker exposure was ascertained from case report forms. Study drug exposure was ascertained from unblinded data from phase III studies. Odds ratios and 95% confidence intervals comparing angioedema risk in vildagliptin-treated and comparator-treated patients were calculated for the overall population and for patients taking ACE inhibitors or angiotensin receptor blockers, using both an analysis of pooled data and a meta-analysis (Peto method). Overall, there was no association between vildagliptin use and angioedema. Among individuals taking an ACE inhibitor, however, vildagliptin use was associated with an increased risk of angioedema (14 confirmed cases among 2754 vildagliptin users versus 1 case among 1819 comparator users: odds ratio 4.57 [95% confidence interval 1.57 to 13.28]) in the meta-analysis. Vildagliptin use may be associated with increased risk of angioedema among patients taking ACE inhibitors, although absolute risk is small. Physicians confronted with angioedema in a patient taking an ACE inhibitor and DPP-IV inhibitor should consider this possible drug-drug interaction.
二肽基肽酶-IV(DPP-IV)抑制剂可减少肠促胰岛素的降解。DPP-IV抑制剂还可减少可能参与血管紧张素转换酶(ACE)抑制剂相关性血管性水肿发病机制的肽类(如P物质)的降解。本研究通过比较在III期随机临床试验中接受DPP-IV抑制剂维格列汀治疗的患者与接受对照药物治疗的患者的血管性水肿发生率,检验了DPP-IV抑制作用影响临床血管性水肿风险这一假设。前瞻性定义的血管性水肿相关事件由内科判定委员会和专家评审员以盲法判定。从病例报告表中确定是否同时使用了ACE抑制剂或血管紧张素受体阻滞剂。研究药物暴露情况从III期研究的非盲数据中确定。使用汇总数据分析和荟萃分析(Peto法),计算维格列汀治疗组和对照药物治疗组患者血管性水肿风险的比值比及95%置信区间,用于总体人群以及服用ACE抑制剂或血管紧张素受体阻滞剂的患者。总体而言,使用维格列汀与血管性水肿之间无关联。然而,在荟萃分析中,在服用ACE抑制剂的个体中,使用维格列汀与血管性水肿风险增加相关(2754例维格列汀使用者中有14例确诊病例,而1819例对照药物使用者中有1例:比值比4.57 [95%置信区间1.57至13.28])。尽管绝对风险较小,但服用ACE抑制剂的患者使用维格列汀可能与血管性水肿风险增加相关。面对服用ACE抑制剂和DPP-IV抑制剂的患者出现血管性水肿的医生应考虑这种可能的药物相互作用。