Vaidyanathan S, Valencia J, Kemp C, Zhao C, Yeh C-M, Bizot M-N, Denouel J, Dieterich H A, Dole W P
Novartis Pharmaceuticals Corporation, East Hanover, NJ, USA.
Int J Clin Pract. 2006 Nov;60(11):1343-56. doi: 10.1111/j.1742-1241.2006.01164.x.
Aliskiren is a novel, orally active direct renin inhibitor that lowers blood pressure alone and in combination with existing antihypertensive agents. As aliskiren does not affect cytochrome P450 enzyme activities, is minimally metabolised, and is not extensively protein bound, the potential for drug interactions is predicted to be low. Four open-label studies investigated the pharmacokinetic interactions between aliskiren 300 mg and the antihypertensive drugs amlodipine 10 mg (n = 18), valsartan 320 mg (n = 18), hydrochlorothiazide 25 mg (HCTZ, n = 22) and ramipril 10 mg (n = 17) in healthy subjects. In each study, subjects received multiple once-daily doses of aliskiren and the test antihypertensive drug alone or in combination in two dosing periods separated by a drug-free washout period. Plasma concentrations of drugs were determined by liquid chromatography and mass spectrometry methods. At steady state, relatively small changes in exposure to aliskiren were observed when aliskiren was co-administered with amlodipine (AUC(tau) increased by 29%, p = 0.032), ramipril (C(max,ss) increased by 31%, p = 0.043), valsartan (AUC(tau) decreased by 26%, p = 0.002) and HCTZ (C(max,ss) decreased by 22%, p = 0.039). Co-administration with aliskiren resulted in small changes in exposure to ramipril (AUC(tau) increased by 22%, p = 0.002), valsartan (AUC(tau) decreased by 14%, p = 0.062) and HCTZ (AUC(tau) decreased by 10% and C(max,ss) by 26%, both p < 0.001). All other changes in pharmacokinetic parameters were also small, and not statistically significant. None of the observed pharmacokinetic changes was considered clinically relevant. Aliskiren inhibited plasma renin activity (PRA) and also prevented the reactive rise in PRA induced by valsartan. The most commonly reported adverse events were headache, dizziness and gastrointestinal symptoms (all mild in severity), which were similar in frequency during antihypertensive drug treatment alone and in combination with aliskiren except for an increase in dizziness during treatment with the combination of aliskiren and HCTZ. In conclusion, aliskiren shows no clinically relevant pharmacokinetic interactions and is generally well tolerated when administered in combination with amlodipine, valsartan, HCTZ or ramipril.
阿利吉仑是一种新型的口服活性直接肾素抑制剂,可单独或与现有抗高血压药物联合使用来降低血压。由于阿利吉仑不影响细胞色素P450酶的活性,代谢极少,且蛋白结合不广泛,预计药物相互作用的可能性较低。四项开放标签研究调查了健康受试者中300毫克阿利吉仑与10毫克氨氯地平(n = 18)、320毫克缬沙坦(n = 18)、25毫克氢氯噻嗪(HCTZ,n = 22)和10毫克雷米普利(n = 17)这几种抗高血压药物之间的药代动力学相互作用。在每项研究中,受试者在两个给药期内接受多次每日一次剂量的阿利吉仑和受试抗高血压药物,单独给药或联合给药,两个给药期之间有一个无药洗脱期。通过液相色谱和质谱法测定药物的血浆浓度。在稳态时,当阿利吉仑与氨氯地平联合使用时,观察到阿利吉仑的暴露量有相对较小的变化(AUC(tau)增加29%,p = 0.032),与雷米普利联合使用时(C(max,ss)增加31%,p = 0.043),与缬沙坦联合使用时(AUC(tau)降低26%,p = 0.002),与氢氯噻嗪联合使用时(C(max,ss)降低22%,p = 0.039)。与阿利吉仑联合给药导致雷米普利的暴露量有小的变化(AUC(tau)增加22%,p = 0.002),缬沙坦的暴露量有小的变化(AUC(tau)降低14%,p = 0.062),氢氯噻嗪的暴露量有小的变化(AUC(tau)降低10%,C(max,ss)降低26%,两者p < 0.001)。药代动力学参数的所有其他变化也都很小,且无统计学意义。观察到的药代动力学变化均未被认为具有临床相关性。阿利吉仑抑制血浆肾素活性(PRA),还可防止缬沙坦诱导的PRA反应性升高。最常报告的不良事件是头痛、头晕和胃肠道症状(均为轻度),单独使用抗高血压药物治疗期间和与阿利吉仑联合使用期间的发生频率相似,但阿利吉仑与氢氯噻嗪联合治疗期间头晕有所增加。总之,阿利吉仑未显示出具有临床相关性的药代动力学相互作用,与氨氯地平、缬沙坦、氢氯噻嗪或雷米普利联合使用时一般耐受性良好。