Comparative Safety of Antiseizure Medication Monotherapy for Major Malformations

dc.contributor.authorCohen Jacqueline M.
dc.contributor.authorAlvestad Silje
dc.contributor.authorCesta Carolyn E.
dc.contributor.authorBjørk Marte-Helene
dc.contributor.authorLeinonen Maarit K.
dc.contributor.authorNørgaard Mette
dc.contributor.authorEinarsdóttir Kristjana
dc.contributor.authorEngeland Anders
dc.contributor.authorGissler Mika
dc.contributor.authorKarlstad Øystein
dc.contributor.authorKlungsøyr Kari
dc.contributor.authorOdsbu Ingvild
dc.contributor.authorReutfors Johan
dc.contributor.authorSelmer Randi M.
dc.contributor.authorTomson Torbjörn
dc.contributor.authorUlrichsen Sinna Pilgaard
dc.contributor.authorZoega Helga
dc.contributor.authorFuru Kari
dc.contributor.organizationfi=lastenpsykiatrian tutkimuskeskus|en=Research Centre for Child Psychiatry|
dc.contributor.organization-code1.2.246.10.2458963.20.83706093164
dc.converis.publication-id178297158
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/178297158
dc.date.accessioned2025-08-28T00:42:50Z
dc.date.available2025-08-28T00:42:50Z
dc.description.abstract<p><strong>Objective:</strong><br></p><p>This study was undertaken to examine the comparative safety of antiseizure medication (ASM) monotherapy in pregnancy with respect to risk of major congenital malformations (MCMs), overall and by MCM subtype.</p><p><strong>Methods:</strong><br></p><p>We conducted a population-based cohort study using national health register data from Denmark, Finland, Iceland, Norway, and Sweden (1996-2020). We compared pregnancies with first trimester exposure to lamotrigine monotherapy to ASM-unexposed, carbamazepine, valproate, oxcarbazepine, levetiracetam, and topiramate to lamotrigine monotherapy, and stratified monotherapy groups by dose. The outcome was nongenetic MCM and specific subtypes. We estimated adjusted risk ratios (aRRs) and 95% confidence intervals (CIs) with log-binomial regression and propensity score weights.</p><p><strong>Results:</strong><br></p><p>There was a higher crude risk of any MCM in pregnancies exposed to lamotrigine monotherapy (n = 8,339) compared to ASM-unexposed pregnancies (n = 4,866,362), but not after confounder adjustment (aRR = 0.97, 95% CI = 0.87-1.08). Compared to lamotrigine, there was an increased risk of malformations associated with valproate (n = 2,031, aRR = 2.05, 95% CI = 1.70-2.46) and topiramate (n = 509, aRR = 1.81, 95% CI = 1.26-2.60), which increased in a dose-dependent manner. We found no differences in malformation risk for carbamazepine (n = 2,674, aRR = 0.91, 95% CI = 0.72-1.15), oxcarbazepine (n = 1,313, aRR = 1.09, 95% CI = 0.83-1.44), or levetiracetam (n = 1,040, aRR = 0.78, 95% CI = 0.53-1.13). Valproate was associated with several malformation subtypes, including nervous system, cardiac, oral clefts, clubfoot, and hypospadias, whereas lamotrigine and carbamazepine were not.</p><p><strong>Interpretation:</strong><br></p><p>Topiramate is associated with an increased risk of MCM similar to that associated with valproate, but lower doses may mitigate the risks for both drugs. Conversely, we found no increased risks for lamotrigine, carbamazepine, oxcarbazepine, or levetiracetam, which is reassuring. ANN NEUROL 2022</p>
dc.identifier.eissn1531-8249
dc.identifier.jour-issn0364-5134
dc.identifier.olddbid206257
dc.identifier.oldhandle10024/189284
dc.identifier.urihttps://www.utupub.fi/handle/11111/45285
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/ana.26561
dc.identifier.urnURN:NBN:fi-fe2023020425855
dc.language.isoen
dc.okm.affiliatedauthorGissler, Mika
dc.okm.discipline3123 Gynaecology and paediatricsen_GB
dc.okm.discipline3124 Neurology and psychiatryen_GB
dc.okm.discipline3123 Naisten- ja lastentauditfi_FI
dc.okm.discipline3124 Neurologia ja psykiatriafi_FI
dc.okm.internationalcopublicationinternational co-publication
dc.okm.internationalityInternational publication
dc.okm.typeA1 ScientificArticle
dc.publisherWILEY
dc.publisher.countryUnited Statesen_GB
dc.publisher.countryYhdysvallat (USA)fi_FI
dc.publisher.country-codeUS
dc.relation.doi10.1002/ana.26561
dc.relation.ispartofjournalAnnals of Neurology
dc.source.identifierhttps://www.utupub.fi/handle/10024/189284
dc.titleComparative Safety of Antiseizure Medication Monotherapy for Major Malformations
dc.year.issued2023

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