The University of Oslo School of Pharmacy, Oslo, Norway The University of Massachusetts Medical School, Worcester, Massachusetts, USA PharmacoEpidemiology and Drug Safety Research Group, Department of Pharmacy, University of Oslo, Oslo, Norway.
The University of Massachusetts Medical School, Worcester, Massachusetts, USA.
BMJ Open. 2016 Sep 13;6(9):e011971. doi: 10.1136/bmjopen-2016-011971.
This study sought to determine whether changes in neurodevelopmental outcomes between 18 and 36 months of age were associated with prenatal exposure to triptan medications, a class of 5-HT receptor agonists used in the treatment of migraine.
Using data from the Norwegian Mother and Child Cohort Study, a prospective birth cohort that includes nearly 40% of all pregnancies in Norway from 1999 to 2008, we identified 50 469 mother-child dyads who met inclusion criteria and were present for at least one follow-up assessment at 18 or 36 months postpartum. Neurodevelopment was assessed using the Child Behaviour Checklist, the Emotionality, Activity, and Shyness Questionnaire, and the Ages and Stages Questionnaire. We used generalised estimating equations to evaluate change from 18 to 36 months for children prenatally exposed to triptans, relative to contrast groups, and used marginal structural models with inverse probability of treatment and censoring weights to address time-varying exposure and confounding as well as loss to follow-up.
Among eligible participants (n=50 469), 1.0% used a triptan during pregnancy, 2.0% used triptans prior to pregnancy only, 8.0% reported migraine without triptan use and 89.0% had no history of migraine. Children with prenatal triptan exposure had greater increases in emotionality (r-RR 2.18, 95% CI 1.03 to 4.53) and activity problems (r-RR 1.70, 95% CI 1.02 to 2.8) compared to children born to mothers who discontinued triptan use prior to pregnancy.
Prenatal triptan exposure was associated with changes over time in externalising-type behaviours such as emotionality and activity, but not with internalising-type behaviours.
本研究旨在探讨 18 至 36 个月时神经发育结局的变化是否与孕期暴露于曲坦类药物有关,曲坦类药物是一类用于治疗偏头痛的 5-HT 受体激动剂。
利用挪威母婴队列研究的数据,这是一项前瞻性出生队列研究,涵盖了 1999 年至 2008 年挪威近 40%的妊娠。我们确定了符合纳入标准且至少在产后 18 或 36 个月进行了一次随访评估的 50469 对母婴对子。使用儿童行为检查表、情绪、活动和害羞问卷以及年龄和阶段问卷评估神经发育。我们使用广义估计方程评估了相对于对照组,从 18 个月到 36 个月儿童的变化,使用逆概率治疗和删失权重的边缘结构模型来解决时间变化的暴露和混杂因素以及失访问题。
在符合条件的参与者中(n=50469),1.0%在孕期使用了曲坦类药物,2.0%仅在孕期前使用了曲坦类药物,8.0%报告有偏头痛但未使用曲坦类药物,89.0%无偏头痛史。与孕期停止使用曲坦类药物的母亲所生的儿童相比,有孕期曲坦类药物暴露的儿童情绪(相对危险比 RR 2.18,95%置信区间 CI 1.03 至 4.53)和活动问题(RR 1.70,95%置信区间 CI 1.02 至 2.8)的增加更为明显。
孕期暴露于曲坦类药物与外部行为(如情绪和活动)随时间的变化有关,但与内部行为无关。