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Prenatal exposure to antiseizure medications and fetal growth: a population-based cohort study from the Nordic countries.
Christensen, Jakob; Zoega, Helga; Leinonen, Maarit K; Gilhus, Nils Erik; Gissler, Mika; Igland, Jannicke; Sun, Yuelian; Tomson, Torbjörn; Alvestad, Silje; Bjørk, Marte-Helene; Dreier, Julie Werenberg.
Afiliación
  • Christensen J; Department of Neurology, Affiliated Member of the European Reference Network EpiCARE, Aarhus University Hospital, Aarhus, Denmark.
  • Zoega H; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
  • Leinonen MK; Centre of Public Health Sciences, Faculty of Medicine, University of Iceland, Reykjavik, Iceland.
  • Gilhus NE; School of Population Health, Faculty of Medicine and Health, UNSW Sydney, Sydney, Australia.
  • Gissler M; Department of Knowledge Brokers, Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Igland J; Department of Clinical Medicine, University of Bergen, Bergen, Norway.
  • Sun Y; Department of Neurology, Haukeland University Hospital, Bergen, Norway.
  • Tomson T; Department of Knowledge Brokers, Finnish Institute for Health and Welfare, Helsinki, Finland.
  • Alvestad S; Region Stockholm, Academic Primary Health Care Centre, Stockholm, Sweden.
  • Bjørk MH; Karolinska Institute, Department of Molecular Medicine and Surgery, Stockholm, Sweden.
  • Dreier JW; Department of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.
Lancet Reg Health Eur ; 38: 100849, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38476755
ABSTRACT

Background:

The short- and long-term consequences of restricted fetal growth cause considerable concern, and how prenatal exposure to different antiseizure medications (ASMs) affects fetal growth remains uncertain.

Methods:

This was a population-based cohort study of liveborn singleton children born in Denmark, Finland, Iceland, Norway, and Sweden from 1996 to 2017. Prenatal exposure was defined as maternal filling of prescriptions for ASM during pregnancy registered in national prescription registries and primary outcomes were adjusted odds ratios (aORs) of microcephaly or being born small for gestational age.

Findings:

We identified 4,494,918 children (males 51.3%, 2,306,991/4,494,918), including 38,714 (0.9%) children of mothers with epilepsy. In the overall population, prenatal monotherapy exposure with carbamazepine (aOR 1.25 (95% CI 1.12-1.40)), pregabalin (aOR 1.16 (95% CI 1.02-1.31)), oxcarbazepine (aOR 1.48 (95% CI 1.28-1.71)), clonazepam (aOR 1.27 (95% CI 1.10-1.48)), and topiramate (aOR 1.48 (95% CI 1.18-1.85)) was associated with risk of being born small for gestational age, and carbamazepine was associated with microcephaly (aOR 1.43 (95% CI 1.17-1.75)). In children of mothers with epilepsy, prenatal exposure to carbamazepine (aOR 1.27 (95% CI 1.11-1.47)), oxcarbazepine (aOR 1.42 (95% CI 1.18-1.70)), clonazepam (aOR 1.40 (95% CI 1.03-1.89)), and topiramate (aOR 1.86 (95% CI 1.36-2.54)) was associated with being born small for gestational age; carbamazepine, with microcephaly (aOR 1.51 (95% CI 1.17-1.95)). No associations with small for gestational age and microcephaly were identified after prenatal exposure to lamotrigine, valproate, gabapentin, levetiracetam, phenobarbital, acetazolamide, phenytoin, clobazam, primidone, zonisamide, vigabatrin, ethosuximide and lacosamide, but except for lamotrigine, valproate, gabapentin, and levetiracetam, numbers of exposed children were small.

Interpretation:

Prenatal exposure to carbamazepine, oxcarbazepine, clonazepam, and topiramate was associated with increased risk of being born small for gestational age in both the overall population and in children of women with epilepsy suggesting that prenatal exposure to these drugs is associated with fetal growth restriction.

Funding:

The NordForsk Nordic Program on Health and Welfare (83539), the Independent Research Fund Denmark (1133-00026B), the Danish Epilepsy Association, the Central Denmark Region, the Novo Nordisk Foundation (NNF16OC0019126 and NNF22OC0075033), and the Lundbeck Foundation (R400-2022-1205).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Lancet Reg Health Eur Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Lancet Reg Health Eur Año: 2024 Tipo del documento: Article País de afiliación: Dinamarca Pais de publicación: Reino Unido