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Risk of early neurodevelopmental disorders associated with in utero exposure to valproate and other antiepileptic drugs: a nationwide cohort study in France
被引:46
|作者:
Coste, Joel
[1
]
Blotiere, Pierre-Olivier
[1
,2
]
Miranda, Sara
[3
]
Mikaeloff, Yann
[4
]
Peyre, Hugo
[5
,6
,7
]
Ramus, Franck
[6
]
Zureik, Mahmoud
[3
,8
]
Weill, Alain
[1
]
Dray-Spira, Rosemary
[3
]
机构:
[1] French Natl Hlth Insurance CNAM, Dept Publ Hlth Studies, Paris, France
[2] Univ Paris 05, Univ Lorraine, Apemac, F-4360 Nancy, EA, France
[3] French Natl Agcy Med & Hlth Prod Safety ANSM, Dept Epidemiol Hlth Prod, St Denis, France
[4] Univ Paris Saclay, Hop Bicetre, INSERM, Villejuif, France
[5] Hop Robert Debre, Dept Child & Adolescent Psychiat, Paris, France
[6] PSL Univ, Lab Sci Cognit & Psycholinguist, Ecole Normale Super, EHESS,CNRS, Paris, France
[7] Paris Diderot Univ, INSERM UMR 1141, Paris, France
[8] Versailles St Quentin Univ, Montigny Le Bretonneux, France
关键词:
D O I:
10.1038/s41598-020-74409-x
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
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.
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