Department of Clinical Pharmacology, Medical Faculty, University of Ostrava and University Hospital, 17.listopadu 1790, 708 52 Ostrava, Czech Republic.
Epilepsy Res. 2010 Oct;91(2-3):161-5. doi: 10.1016/j.eplepsyres.2010.07.007. Epub 2010 Aug 7.
We followed up lamotrigine transport through the placenta and analyzed maternal and umibilical cord concentrations, its ratio and maternal lamotrigine clearance in monotherapy and in combinations.
Maternal and umbilical cord concentrations were analyzed during delivery in a cohort of 63 women between 2001 and 2009. The request forms for routine therapeutic drug monitoring were used as the data source. Maternal concentrations were used for the estimation of apparent oral clearance and paired infant and maternal concentrations for estimation of the infant (umibilical cord)/maternal serum concentration ratio.
The lamotrigine infant/maternal serum concentration ratio ranged in monotherapy from 0.40 to 1.38 (median 0.91). The ratio in monotherapy showed a possible distribution to two subgroups. Concomitant administration of valproic acid significantly increased both maternal and infant lamotrigine concentrations and significantly decreased lamotrigine clearance by about 65%. Co-medication with carbamazepine increased lamotrigine clearance non-significantly. Highly significant correlations were found between maternal and umbilical cord lamotrigine concentrations, both in monotherapy and in the lamotrigine+valproic acid combination. Infant concentrations of valproic acid were found to be about 30% higher and infant concentrations of carbamazepine were found to be about 20% lower than maternal concentrations.
Our data from the large cohort showed the interindividual variability of umbilical cord/maternal serum concentration ratio in lamotrigine monotherapy caused probably by the different activity of the placental lamotrigine metabolizing enzymes UGT1A4 and 2B7 associated with genetic polymorphism. The potential teratogenic effect of lamotrigine combination with valproic acid could be associated with the higher lamotrigine and valproic acid concentrations in the fetus.
我们对拉莫三嗪在胎盘内的转运进行了随访,并分析了单药治疗和联合治疗时母体和脐血中的浓度、其比值以及母体拉莫三嗪清除率。
在 2001 年至 2009 年间,我们对 63 名女性在分娩时的母体和脐血浓度进行了分析。数据来源于常规治疗药物监测的申请单。我们利用母体浓度来估算表观口服清除率,利用婴儿和母体的配对浓度来估算婴儿(脐血)/母体血清浓度比值。
单药治疗时,拉莫三嗪婴儿/母体血清浓度比值范围为 0.40 至 1.38(中位数为 0.91)。该比值在单药治疗时可能存在两个亚组分布。丙戊酸的联合应用显著增加了母体和婴儿的拉莫三嗪浓度,并使拉莫三嗪清除率显著降低了约 65%。卡马西平的合并用药使拉莫三嗪清除率无显著增加。母体和脐血拉莫三嗪浓度之间存在高度显著的相关性,无论是在单药治疗还是在拉莫三嗪+丙戊酸联合治疗时。丙戊酸的婴儿浓度比母体浓度高约 30%,而卡马西平的婴儿浓度比母体浓度低约 20%。
我们从大型队列中获得的数据显示,在拉莫三嗪单药治疗中,脐血/母体血清浓度比值存在个体间的变异性,这可能是由于与遗传多态性相关的胎盘拉莫三嗪代谢酶 UGT1A4 和 2B7 的不同活性所致。拉莫三嗪与丙戊酸联合治疗的潜在致畸作用可能与胎儿中拉莫三嗪和丙戊酸浓度较高有关。