Concerns regarding lamotrigine and breast-feeding

被引:46
作者
Liporace, J [1 ]
Kao, A
D'Abreu, A
机构
[1] Jefferson Med Coll, Dept Neurol, Philadelphia, PA 19107 USA
[2] Childrens Hosp Philadelphia, Dept Neurol, Philadelphia, PA 19104 USA
关键词
lamotrigine; epilepsy; breast-feeding; glucuronidation;
D O I
10.1016/j.yebeh.2003.11.018
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Purpose. Many women with epilepsy who are planning a pregnancy are treated with lamotrigine (LTG), resulting in greater fetal exposure to the drug. Current care guidelines suggest that mothers with epilepsy breast-feed their children. These recommendations are made without regard to how nursing newborns metabolize medication. Lamotrigine is extensively metabolized by glucuronidation, which is immature in neonates and may lead to accumulation of medication. This article reports LTG levels in full-term nursing newborns born to mothers with epilepsy on lamotrigine monotherapy. Methods. Serum LTG levels were obtained in nursing mothers and their neonates on Day 10 of life. Maternal LTG clearance during pregnancy and postpartum was determined and correlated with levels. Results. Four mothers with partial epilepsy on LTG monotherapy were evaluated. Serum LTG levels in nursing newborns ranged from <1.0 to 2.0 mug/mL on Day 10 of life. Three babies had LTG levels >1.0 mug/mL. After excluding one child with an undetectable level, the LTG levels in newborns were on average 30% (range 20-43%) of the maternal drug level. No decline was noted in two children with repeat levels at 2 months. Conclusion. Serum concentrations of LTG in breast-fed children were higher than expected, in some cases reaching "therapeutic" ranges. These high levels may be explained by poor neonatal drug elimination due to inefficient glucuronidation. Our observation that not all newborns had a high LTG level suggests considerable genetic variability in metabolism. Our limited data suggest monitoring blood levels in nursing children and the need for individual counseling for women with epilepsy regarding breast-feeding. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:102 / 105
页数:4
相关论文
共 16 条
[1]  
BOCK KW, 1988, BIOCHEM PHARMACOL, V37, P987
[2]  
COUGHTRIE MWH, 1988, MOL PHARMACOL, V34, P729
[3]  
Garnett WR, 1997, J CHILD NEUROL S1, V12, P10
[4]  
Greenberg MK, 1998, EPILEPSIA, V39, P1226
[5]   Drug glucuronidation in clinical psychopharmacology [J].
Liston, HL ;
Markowitz, JS ;
DeVane, CL .
JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2001, 21 (05) :500-515
[6]   DRUG GLUCURONIDATION IN HUMANS [J].
MINERS, JO ;
MACKENZIE, PI .
PHARMACOLOGY & THERAPEUTICS, 1991, 51 (03) :347-369
[7]   ANTI-CONVULSANTS DURING PREGNANCY AND LACTATION - TRANS-PLACENTAL, MATERNAL AND NEONATAL PHARMACOKINETICS [J].
NAU, H ;
KUHNZ, W ;
EGGER, HJ ;
RATING, D ;
HELGE, H .
CLINICAL PHARMACOKINETICS, 1982, 7 (06) :508-543
[8]   Lamotrigine in pregnancy: Pharmacokinetics during delivery, in the neonate, and during lactation [J].
Ohman, I ;
Vitols, S ;
Tomson, T .
EPILEPSIA, 2000, 41 (06) :709-713
[9]   DRUG-METABOLISM IN PREGNANCY, INFANCY AND CHILDHOOD [J].
PERUCCA, E .
PHARMACOLOGY & THERAPEUTICS, 1987, 34 (01) :129-143
[10]   Concentrations of lamotrigine in a mother on lamotrigine treatment and her newborn child [J].
Rambeck, B ;
Kurlemann, G ;
Stodieck, SRG ;
May, TW ;
Jurgens, U .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1997, 51 (06) :481-484