Bromfield Edward B, Dworetzky Barbara A, Wyszynski Diego F, Smith Caitlin R, Baldwin Elizabeth J, Holmes Lewis B
Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Epilepsia. 2008 Dec;49(12):2122-4. doi: 10.1111/j.1528-1167.2008.01696.x. Epub 2008 Jun 13.
Maternal valproate (VPA) use is associated with a significant risk for congenital malformations in the exposed fetus. Since VPA is commonly used in epilepsy syndromes with a presumed genetic cause (idiopathic epilepsies), it is possible that maternal genetic background contributes to this outcome. We reviewed responses to telephone questionnaires and medical records, when available, of enrollees in the North American Antiepileptic Drug Pregnancy Registry, classifying reason for treatment as idiopathic generalized epilepsy (IGE), partial epilepsy (PE), nonclassifiable epilepsy (NCE), or not epilepsy (NE). Of 284 VPA-exposed pregnancies, 30 (11.0%) were associated with malformations: IGE = 15/126 (12%), PE = 4/28 (14%), NCE = 9/105 (9%), NE = 2/25 (8%) (p > 0.7 for all comparisons). There was a trend toward increased malformation risk with higher VPA doses (p = 0.07). VPA, and not the underlying genetic syndrome, seems to be associated with the elevated risk for malformations in the drug-exposed fetus.
母亲使用丙戊酸(VPA)与暴露胎儿发生先天性畸形的重大风险相关。由于VPA常用于推测有遗传病因的癫痫综合征(特发性癫痫),母亲的遗传背景可能导致了这一结果。我们回顾了北美抗癫痫药物妊娠登记处登记人员的电话调查问卷回复及可用的病历,将治疗原因分类为特发性全身性癫痫(IGE)、部分性癫痫(PE)、不可分类癫痫(NCE)或非癫痫(NE)。在284例暴露于VPA的妊娠中,30例(11.0%)与畸形相关:IGE = 15/126(12%),PE = 4/28(14%),NCE = 9/105(9%),NE = 2/25(8%)(所有比较p>0.7)。随着VPA剂量增加,畸形风险有升高趋势(p = 0.07)。似乎是VPA,而非潜在的遗传综合征,与暴露于药物的胎儿畸形风险升高相关。