Plasma concentrations of risperidone and 9-hydroxyrisperidone:: Effect of comedication with carbamazepine or valproate

被引:105
|
作者
Spina, E
Avenoso, A
Facciolà, G
Salemi, M
Scordo, MG
Giacobello, T
Madia, AG
Perucca, E
机构
[1] Univ Messina, Policlin Univ, Inst Pharmacol, I-98125 Messina, Italy
[2] Azienda USL 5, Ctr Mental Hlth, Messina, Italy
[3] Univ Pavia, Dept Internal Med, Clin Pharmacol Unit, Ctr Mental Hlth, I-27100 Pavia, Italy
关键词
risperidone; 9-hydroxyrisperidone; carbamazepine; valproic acid; drug interaction; CYP3A4;
D O I
10.1097/00007691-200008000-00019
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
To evaluate the pharmacokinetic interaction between risperidone and the mood-stabilizing agents carbamazepine and valproic acid, steady state plasma concentrations of risperidone and 9-hydroxyrisperidone (9-OH-risperidone) were compared in patients treated with risperidone alone (controls, n = 23) and in patients comedicated matched for sex, age, body weight, and antipsychotic dosage. Plasma concentrations of risperidone and 9-OH-risperidone did not differ between valproate-comedicated patients and controls. By contrast, the concentrations of both compounds were lower in patients taking carbamazepine, although the difference reached statistical significance only for the metabolite (p < 0.001). The sum of the concentrations of risperidone and 8-OH-risperidone in patients receiving carbamazepine (median 44 nmol/L) was also significantly lower than in patients receiving valproate (168 nmol/L) and in controls (150 nmol/L), In five patients assessed with and without carbamazepine comedication, dose-normalized plasma risperidone and 9-OH-risperidone concentrations were significantly lower when the patients received combination therapy than when they received risperidone alone. In three patients assessed witt and without valproate, no major changes in the levels of risperidone and its metabolite were observed. These findings demonstrate that carbamazepine markedly decreases the plasma concentrations of risperidone and its active 9-OH-metabolite, probably by inducing CYP3A4-mediated metabolism. This interaction is likely to be clinically significant. Conversely, valproic acid does not cause any major change in plasma antipsychotic levels.
引用
收藏
页码:481 / 485
页数:5
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