Evidence map›Paper›PMID 41876129›Full record

ArticleJournal of neurology, neurosurgery, and psychiatry2026

Timing of high-dose folic acid supplementation in the periconceptional period among women taking antiseizure medications and risk of major congenital anomalies: a target trial emulation.

Yuelian Sun, Silje Alvestad, Jacqueline M Cohen, Jannicke Igland, Nils Erik Gilhus, Håkon M Vegrim, Torbjörn Tomson, Jakob Christensen, Maarit K Leinonen, Mika Gissler and 4 more

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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0cells of the map it votes in
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

14 authors.

Yuelian SunDepartment of Neurology, Aarhus University Hospital, Affiliated Member of Epi-Care, Aarhus, Denmark ys@clin.au.dk.ORCID http://orcid.org/0000-0002-6905-0503
Silje AlvestadDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.
Jacqueline M CohenDepartment of Chronic Diseases, Norwegian Institute of Public Health, Oslo, Norway.ORCID http://orcid.org/0000-0002-7300-0488
Jannicke IglandDepartment of Global Public Health and Primary Care, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0002-2289-0978
Nils Erik GilhusDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.ORCID http://orcid.org/0000-0001-6522-5102
Håkon M VegrimDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.
Torbjörn TomsonDepartment of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Jakob ChristensenDepartment of Neurology, Aarhus University Hospital, Affiliated Member of Epi-Care, Aarhus, Denmark.
Maarit K LeinonenDepartment of Data and Analytics, Finnish Institute for Health and Welfare, Helsinki, Finland.ORCID http://orcid.org/0000-0002-7631-4749
Mika GisslerDepartment of Data and Analytics, Finnish Institute for Health and Welfare, Helsinki, Finland.ORCID http://orcid.org/0000-0001-8254-7525
Helga ZoegaCentre of Public Health Sciences, Faculty of Medicine, University of Iceland, Reykjavík, Iceland.
Neda RazazDivision of Clinical Epidemiology, Department of Medicine Solna, Karolinska Institute, Solna, Sweden.ORCID http://orcid.org/0000-0002-1273-0110
Julie Werenberg Dreier *National Centre for Register-Based Research, Aarhus University, Aarhus, Denmark.
Marte-Helene Bjørk *Department of Clinical Medicine, University of Bergen, Bergen, Norway.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh-dose folic acid supplementation is recommended for women using antiseizure medication (ASMs) to reduce risk of major congenital anomalies (MCAs) in offspring, but evidence is lacking.

methodsWe conducted a sequential target trial emulation using nationwide register data from Denmark, Iceland, Norway, and Sweden (1997-2020). Eligible women using ASMs were included and classified as initiators or non-initiators based on whether they filled prescription for high-dose folic acid within one week of inclusion. Risk difference (RD) and risk ratio (RR) for MCAs diagnosed before one year of age in offspring were estimated for initiators of high-dose folic acid (4 or 5 mg/day) supplementation in three periconceptional periods (13-52 weeks before, 1-12 weeks before, and 1-12 weeks after pregnancy onset) compared with non-initiators.

resultsWe included 18 255, 13 619, and 12 365 eligible pregnancies and identified 1047 (5.7%), 521 (3.8%) and 1778 (14.4%) initiators of high-dose folic acid in the three periods, respectively. Initiation of high-dose folic acid 1-12 weeks before pregnancy was associated with a lower prevalence of MCA in offspring (2.6% vs 4.8% among non-initiators), corresponding to an absolute risk reduction of 2.2 percentage points (95% CI 0.5 to 3.5) and a 45% relative risk reduction (RR=0.55, 95% CI 0.25 to 0.91). No risk reduction was observed with initiation 1-12 weeks after (RR=1.27, 95% CI 0.94 to 1.64) or 13-52 weeks before (RR=0.99, 95% CI 0.65 to 1.36) pregnancy onset.

conclusionsInitiation of high-dose folic acid in the 12 weeks before pregnancy was associated with a reduced risk of MCA in offspring of women using ASMs while initiation in the 12 weeks after pregnancy onset was not. RESEARCH PROTOCOL REGISTRATION: https://osf.io/vph2n/?view_only=c9361e4996eb4c4da32fc878f2fbf5b9.

Indexed as

Abnormalities, Drug-InducedAnticonvulsantsDietary SupplementsEpilepsyFolic AcidAdultFemaleHumansPregnancyRegistriesTime FactorsAnticonvulsantsFolic AcidEPIDEMIOLOGYEPILEPSY

Identifiers

PMID41876129
PMCPMC13227143

What OpenQuestion holds

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Registered trials

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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.