Unger Thomas, Kaschina Elena
Institute of Pharmacology and Toxicology, Charité Hospital, Humboldt University at Berlin, Berlin, Germany.
Drug Saf. 2003;26(10):707-20. doi: 10.2165/00002018-200326100-00004.
The ever-increasing introduction of new therapeutic agents means that the potential for drug interactions is likely to escalate. Numerous different classes of drugs are currently used to treat hypertension. The angiotensin receptor blockers offer one of the newest approaches to the management of patients with high blood pressure. Compared with other classes of antihypertensive agents, the angiotensin receptor blockers appear overall to have a low potential for drug interactions, but variations within the class have been detected. Losartan and irbesartan have a greater affinity for cytochrome p450 (CYP) isoenzymes and, thus, are more likely to be implicated in drug interactions. There is pharmacokinetic evidence to suggest that such interactions could have a clinical impact. Candesartan cilexetil, valsartan and eprosartan have variable but generally modest affinity and telmisartan has no affinity for any of the CYP isoenzymes. In vitro studies and pharmacokinetic/pharmacodynamic evaluation can provide evidence for some interactions, but only a relatively small number of drug combinations are usually studied in this way. The absence of any pharmacokinetic evidence of drug interaction, however, should not lead to complacency. Patients should be made aware of possible interactions, especially involving the concurrent use of over-the-counter products, and it may be prudent for all patients receiving antihypertensive treatment to be monitored for possible drug interactions at their regular check-ups. The physician can help by prescribing agents with a low potential for interaction, such as angiotensin receptor blockers.
新治疗药物的不断引入意味着药物相互作用的可能性可能会增加。目前有许多不同类别的药物用于治疗高血压。血管紧张素受体阻滞剂为高血压患者的管理提供了一种最新的方法。与其他类别的抗高血压药物相比,血管紧张素受体阻滞剂总体上似乎药物相互作用的可能性较低,但已发现该类别内部存在差异。氯沙坦和厄贝沙坦对细胞色素P450(CYP)同工酶具有更高的亲和力,因此更有可能与药物相互作用有关。有药代动力学证据表明此类相互作用可能具有临床影响。坎地沙坦酯、缬沙坦和依普罗沙坦具有可变但通常适度的亲和力,而替米沙坦对任何CYP同工酶均无亲和力。体外研究和药代动力学/药效学评估可为某些相互作用提供证据,但通常仅以这种方式研究相对较少的药物组合。然而,缺乏任何药物相互作用的药代动力学证据不应导致自满。应让患者了解可能的相互作用,尤其是涉及同时使用非处方药产品的情况,对于所有接受抗高血压治疗的患者,在定期检查时监测可能的药物相互作用可能是谨慎的做法。医生可以通过开具相互作用可能性低的药物,如血管紧张素受体阻滞剂来提供帮助。