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DOI 10.1016/j.dmpk.2015.01.001

Медицинская библиотека · Drug metabolism and pharmacokinetics · 2015

Influence of uridine diphosphate glucuronosyltransferase inducers and inhibitors on the plasma lamotrigine concentration in pediatric patients with refractory epilepsy.

Yamamoto Yoshiaki, Takahashi Yukitoshi, Imai Katsumi, Ikeda Hiroko, Takahashi Masaaki, Nakai Masahiko, Inoue Yushi, Kagawa Yoshiyuki

СтатьяПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

This study evaluated the influence of concomitant antiepileptic drugs (AEDs) on the plasma concentration of lamotrigine (LTG) in pediatric patients with epilepsy. We retrospectively reviewed 1653 plasma samples from 709 patients (aged 6 months to 16 years) and compared the concentration-to-dose ratio (CD ratio) of LTG among different AED regimens. The median CD ratio of patients receiving LTG monotherapy was 1.25 μg/mL/mg/kg. In patients receiving LTG plus VPA, the CD ratio was increased by about 140%. The CD ratio was elevated from a low VPA concentration (<40 μg/mL) and the increase was VPA concentration-dependent. In contrast, the median CD ratio of patients treated with LTG plus the inducers phenytoin, phenobarbital, and carbamazepine was 0.42, 0.63, and 0.66, respectively, and phenytoin significantly reduced the CD ratio in comparison with phenobarbital or carbamazepine (p < 0.001). Pediatric patients of all ages beyond infancy showed similar susceptibility to VPA or inducers, but infants had higher CD ratios compared with the other age groups. Among other AEDs, topiramate, ethosuximide, and rufinamide reduced the CD ratio. These findings should be useful for estimating interactions between LTG and concomitant AEDs.

Для цитирования: Yamamoto Yoshiaki, Takahashi Yukitoshi, Imai Katsumi, Ikeda Hiroko, Takahashi Masaaki, Nakai Masahiko, Inoue Yushi, Kagawa Yoshiyuki. Influence of uridine diphosphate glucuronosyltransferase inducers and inhibitors on the plasma lamotrigine concentration in pediatric patients with refractory epilepsy.. Drug metabolism and pharmacokinetics. 2015. DOI: 10.1016/j.dmpk.2015.01.001.

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