Hachad Houda, Ragueneau-Majlessi Isabelle, Levy Rene H
Department of Pharmaceutics, University of Washington, Seattle, Washington 98195, USA.
Ther Drug Monit. 2002 Feb;24(1):91-103. doi: 10.1097/00007691-200202000-00016.
During the Past decade, nine new antiepileptic drugs (AEDs) namely, Felbamate, Gabapentin, Levetiracetam, Lamotrigine, Oxcarbazepine, Tiagabine, Topiramate, Vigabatrin and Zonisamide have been marketed worldwide. The introduction of these drugs increased appreciably the number of therapeutic combinations used in the treatment of epilepsy and with it, the risk of drug interactions. In general, these newer antiepileptic drugs exhibit a lower potential for drug interactions than the classic AEDs, like phenytoin, carbamazepine and valproic acid, mostly because of their pharmacokinetic characteristics. For example, vigabatrin, levetiracetam and gabapentin, exhibit few or no interactions with other AEDs. Felbamate, tiagabine, topiramate and zonisamide are sensitive to induction by known anticonvulsants with inducing effects but are less vulnerable to inhibition by common drug inhibitors. Felbamate, topiramate and oxcarbazepine are mild inducers and may affect the disposition of oral contraceptives with a risk of failure of contraception. These drugs also inhibit CYP2C19 and may affect the disposition of phenytoin. Lamotrigine is eliminated mostly by glucuronidation and is susceptible to inhibition by valproic acid and induction by classic AEDs such as phenytoin, carbamazepine, phenobarbital and primidone.
在过去十年间,九种新型抗癫痫药物(AEDs),即非氨酯、加巴喷丁、左乙拉西坦、拉莫三嗪、奥卡西平、噻加宾、托吡酯、氨己烯酸和唑尼沙胺已在全球上市。这些药物的引入显著增加了用于治疗癫痫的治疗组合数量,随之也增加了药物相互作用的风险。总体而言,这些新型抗癫痫药物与苯妥英、卡马西平和丙戊酸等经典抗癫痫药物相比,药物相互作用的可能性较低,这主要是由于它们的药代动力学特征。例如,氨己烯酸、左乙拉西坦和加巴喷丁与其他抗癫痫药物几乎没有或不存在相互作用。非氨酯、噻加宾、托吡酯和唑尼沙胺对具有诱导作用的已知抗惊厥药的诱导敏感,但对常见药物抑制剂的抑制作用较不敏感。非氨酯、托吡酯和奥卡西平是轻度诱导剂,可能会影响口服避孕药的代谢,存在避孕失败的风险。这些药物还会抑制CYP2C19,可能会影响苯妥英的代谢。拉莫三嗪主要通过葡萄糖醛酸化代谢,易受丙戊酸抑制,以及苯妥英、卡马西平、苯巴比妥和扑米酮等经典抗癫痫药物的诱导。