Evidence map›Paper›PMID 41781215›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2026

Risk of neurodevelopmental disorders associated with paternal use of valproate during spermatogenesis.

Neda Razaz, Jonas Soderling, Torbjörn Tomson, Julie Werenberg Dreier, Jakob Christensen, Marte-Helene Bjørk, Jannicke Igland

Abstract read
In one paragraph

Article in Journal of neurology, neurosurgery, and psychiatry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Neda RazazDivision of Clinical Epidemiology, Karolinska University Hospital, Stockholm, Sweden Neda.razaz@ki.se.ORCID http://orcid.org/0000-0002-1273-0110
Jonas SoderlingDivision of Clinical Epidemiology, Karolinska University Hospital, Stockholm, Sweden.
Torbjörn TomsonClinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-0554-5352
Julie Werenberg DreierCentre for Integrated Register-based Research, Aarhus University, Aarhus, Denmark.
Jakob ChristensenDepartment of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Marte-Helene BjørkDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.
Jannicke IglandDepartment of Neurology, Haukeland University Hospital, Bergen, Norway.ORCID http://orcid.org/0000-0002-2289-0978

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRegulatory authorities have raised concerns about potential teratogenic and neurodevelopmental disorders (NDDs) risks associated with paternal valproate use during spermatogenesis, leading to restrictions. We aimed to investigate the association between paternal valproate exposure during spermatogenesis and the risk of NDDs in offspring in Sweden and Norway.

methodsWe conducted a population-based cohort study of two nationwide cohorts from Sweden and Norway, including all singleton live births (≥22 gestational weeks) from 2007 to 2020. Paternal monotherapy exposure to valproate, lamotrigine or levetiracetam was defined as ≥1 prescription filled for only one of these medications during the 3 months prior to conception. NDDs were identified from health registers from age 1 through 2022. Cox proportional hazards models were used to estimate adjusted HRs (aHRs), accounting for relevant confounders. A random-effects meta-analysis combined results from both countries.

resultsThe Swedish cohort included 1588 children with paternal valproate and 3093 with lamotrigine/levetiracetam monotherapy, while the Norwegian cohort included 463 and 1109, respectively. Compared with paternal lamotrigine/levetiracetam monotherapy, paternal valproate exposure was not associated with increased pooled risk of any NDD (aHR, 1.06; 95% CI 0.81 to 1.22), including autism spectrum disorder (aHR, 1.29; 95% CI 0.89 to 1.85), attention-deficit/hyperactivity disorder (aHR, 0.98; 95% CI 0.76 to 1.25), intellectual disability (aHR, 1.20; 95% CI 0.65 to 2.21; Sweden only) or psychological development disorders (aHR, 1.28; 95% CI 0.84 to 1.97). Findings remained consistent in dose-response analyses and when restricted to fathers with epilepsy.

conclusionsIn this large Nordic study, paternal valproate use during spermatogenesis was not associated with increased risk of NDDs in offspring, suggesting current regulatory restrictions may warrant re-evaluation.

Indexed as

AnticonvulsantsNeurodevelopmental DisordersPaternal ExposurePrenatal Exposure Delayed EffectsSpermatogenesisValproic AcidAdultChildChild, PreschoolCohort StudiesEpilepsyFemaleHumansInfantLamotrigineLevetiracetamAnticonvulsantsLamotrigineLevetiracetamValproic AcidEPIDEMIOLOGYEPILEPSYNEUROEPIDEMIOLOGY

Identifiers

PMID41781215
PMCPMC13479227

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.