Department of Public Health Studies, French National Health Insurance (CNAM), Paris, France.
Université de Lorraine, Université Paris-Descartes, Apemac, 4360, Nancy, EA, France.
Sci Rep. 2020 Oct 22;10(1):17362. doi: 10.1038/s41598-020-74409-x.
Information available on the risks of neurodevelopmental disorders (NDs) associated with in utero exposure to valproate (VPA) and to other antiepileptic drugs (AEDs) is limited. A nationwide population-based cohort study was conducted based on comprehensive data of the French National Health Data System (SNDS). Liveborn infants without brain malformation, born between January 2011 and December 2014, were followed from birth up to December 2016. NDs were identified based on diagnoses of mental or behavioural disorders and utilization of speech therapy, orthoptic or psychiatric services. The risk of NDs was compared between children exposed in utero to AED monotherapy and unexposed children, using Cox proportional hazard models adjusted for maternal and neonatal characteristics. The cohort included 1,721,990 children, 8848 of whom were exposed in utero to AED monotherapy. During a mean follow-up of 3.6 years, 15,458 children had a diagnosis of mental or behavioural disorder. In utero exposure to VPA was associated with an increased risk of NDs overall (aHR: 3.7; 95% CI 2.8-4.9) and among children born to a mother without mental illness (aHR 5.1; 95% CI 3.6-7.3). A dose-response relationship was demonstrated and the risk of NDs was more particularly increased for an exposure to VPA during the second or third trimesters of pregnancy. Among the other AEDs, only pregabalin was consistently associated with an increased risk of NDs (aHR: 1.5; 95% CI 1.0-2.1). This study confirms a four to fivefold increased risk of early NDs associated with exposure to VPA during pregnancy. The risk associated with other AEDs appears much lower.
有关与胎儿暴露于丙戊酸(VPA)和其他抗癫痫药物(AED)相关的神经发育障碍(NDs)风险的信息有限。一项基于法国国家健康数据系统(SNDS)综合数据的全国性基于人群的队列研究得以开展。本研究对 2011 年 1 月至 2014 年 12 月间出生的无脑畸形的活产婴儿进行了随访,随访时间截至 2016 年 12 月。NDs 通过精神或行为障碍的诊断以及言语治疗、斜视或精神科服务的使用来确定。使用 Cox 比例风险模型,根据母亲和新生儿特征对暴露于宫内 AED 单药治疗的儿童与未暴露于宫内 AED 单药治疗的儿童的 NDs 风险进行了比较。该队列纳入了 1721990 名儿童,其中 8848 名儿童在宫内暴露于 AED 单药治疗。在平均 3.6 年的随访期间,有 15458 名儿童被诊断患有精神或行为障碍。总的来说,胎儿暴露于 VPA 与 NDs 的风险增加相关(aHR:3.7;95%CI 2.8-4.9),在母亲无精神疾病的儿童中,风险增加更为明显(aHR:5.1;95%CI 3.6-7.3)。研究结果显示了一种剂量反应关系,并且在妊娠的第二或第三个三个月暴露于 VPA 与 NDs 的风险增加尤其相关。在其他 AED 中,只有普瑞巴林与 NDs 的风险增加相关(aHR:1.5;95%CI 1.0-2.1)。本研究证实,与怀孕期间暴露于 VPA 相关的早期 NDs 的风险增加了四到五倍。与其他 AED 相关的风险似乎要低得多。