Evidence map›Paper›PMID 42230530›Full record

ArticleDrug safety2026

Gabapentin and Pregabalin Use in First Trimester of Pregnancy and Risk of Specific Congenital Anomalies: An IMI ConcePTION European Case-Malformed Control Study.

Anna-Belle Beau, Erika Cifuentes Castro, Justine Benevent, Marie Beslay, Laia Barrachina-Bonet, Jorieke E H Bergman, Clara Cavero-Carbonell, Alessio Coi, Helen Dolk, Ester Garne and 12 more

Abstract read
In one paragraph

Article in Drug safety, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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

22 authors.

Anna-Belle BeauCERPOP, Inserm U1295, Université de Toulouse Paul Sabatier, Service de Pharmacologie Clinique, CHU de Toulouse, 37 allées Jules Guesde Bat C, floor 3, 31000, Toulouse, France. anna-belle.beau@univ-tlse3.fr.ORCID http://orcid.org/0000-0003-4631-100X
Erika Cifuentes CastroCERPOP, Inserm U1295, Université de Toulouse Paul Sabatier, Service de Pharmacologie Clinique, CHU de Toulouse, 37 allées Jules Guesde Bat C, floor 3, 31000, Toulouse, France.
Justine BeneventCERPOP, Inserm U1295, Université de Toulouse Paul Sabatier, Service de Pharmacologie Clinique, CHU de Toulouse, 37 allées Jules Guesde Bat C, floor 3, 31000, Toulouse, France.
Marie BeslayCERPOP, Inserm U1295, Université de Toulouse Paul Sabatier, Service de Pharmacologie Clinique, CHU de Toulouse, 37 allées Jules Guesde Bat C, floor 3, 31000, Toulouse, France.
Laia Barrachina-BonetRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Jorieke E H BergmanDepartment of Genetics, EUROCAT Northern Netherlands, University of Groningen, University Medical Center Groningen, Groningen, Netherlands.
Clara Cavero-CarbonellRare Diseases Research Unit, Foundation for the Promotion of Health and Biomedical Research in the Valencian Region, Valencia, Spain.
Alessio CoiUnit of Epidemiology of Rare Diseases and Congenital Anomalies. Institute of Clinical Physiology, National Research Council, Pisa, Italy.
Helen DolkSchool of Medicine, Ulster University, Belfast, United Kingdom.
Ester GarneDepartment of Paediatrics and Adolescent Medicine, Lillebaelt Hospital, University Hospital of Southern Denmark, Kolding, Denmark.
Miriam GattMalta Congenital Anomalies Registry, Directorate for Health Information and Research, Pietà, Malta.
Jonathan HoareauUnit of congenital malformations, REMACOR- Medical School University of La Réunion St Pierre, Sainte-Clotilde, France.
Elly Den HondProvincial Institute of Hygiene, Antwerp, Belgium.
Anna Latos-BielenskaDepartment of Medical Genetics, Poznan University of Medical Sciences, Poznań, Poland.
Nathalie LelongParis Registry of Congenital Malformations, Obstetrical, Perinatal and Paediatric Epidemiology Research Team, INSERM, UMR 1153, Paris, France.
Mary O'MahonyDepartment of Public Health, Health Service Executive-South, Cork, Ireland.
Xavier MoissetUniversité Clermont Auvergne, CHU de Clermont-Ferrand, Inserm, Neuro-Dol, Clermont-Ferrand, France.
Joan MorrisPopulation Health Research Institute, St George's, University of London, London, United Kingdom.
Amanda J NevilleIMER Registry (Emilia Romagna Registry of Birth Defects, Centre for Clinical and Epidemiological Research, University of Ferrara, Azienda, Ospedaliero Universitaria di Ferrara, Ferrara, Italy.
Joanna SichitiuDepartment of Woman-Mother-Child, University Hospital Center CHUV, 1011, Lausanne, Switzerland.
Maria LoaneInstitute of Nursing and Health Research, Ulster University, Belfast, United Kingdom.
Christine Damase-MichelCERPOP, Inserm U1295, Université de Toulouse Paul Sabatier, Service de Pharmacologie Clinique, CHU de Toulouse, 37 allées Jules Guesde Bat C, floor 3, 31000, Toulouse, France.

Funding

Innovative Medicines Initiative 821520
6 · The paper itself

Abstract

INTRODUCTION AND

objectiveGiven the increasing use of gabapentinoids and ongoing safety concerns, we assessed the association between first-trimester exposure to gabapentin and pregabalin and the risk of specific congenital anomalies (CAs) in the offspring.

methodsUsing EUROmediCAT data, we conducted a case-malformed control study based on 170,126 registrants with major CAs from livebirths, fetal deaths (≥20 weeks), and terminations of pregnancy for fetal anomaly in nine European countries (2000-2020), covering 10.6 million births. We compared gabapentinoid use in registrants with a specific CA with those among other registrants with non-genetic CA (main control group) and among registrants with a genetic condition (secondary control group). We estimated odds ratios (OR) and 95% confidence intervals (CI), adjusting for registry, birth year, and maternal age. Analyses included specific subgroups of CA with ≥3 exposed registrants.

resultsFirst-trimester gabapentinoid exposure was identified in 37 registrants, with most registered in the Valencian region (Spain) (37.8%), EFEMERIS (France) (13.5%) and three other registries (8.1% each). Over 60% of the exposures were observed during 2015-2020. Seven out of 91 EUROCAT subgroups had ≥3 exposed registrants: congenital heart defects, ventricular septal defects, severe congenital heart defects, limb anomalies, urinary anomalies, genital anomalies, and hypospadias. A significantly higher proportion of exposure (0.4‰, 12 exposed cases) was observed among cases with ventricular septal defect compared with registrants in the non-genetic control group (0.2‰, 17 exposed cases), with an adjusted OR of 2.5 (95% CI 1.1-5.3); and the adjusted OR was elevated but non-significant compared with the registrants in the genetic group (2.3; 95% CI 0.8-6.9).

conclusionsWe observed an association between first trimester exposure to gabapentinoids and ventricular septal defect, the most common cardiac anomaly, although this finding is based on only 37 exposed registrants. While our findings align with some previous studies suggesting teratogenic risks associated with gabapentinoids, they also reveal the challenges of studying rare exposures and rare outcomes.

Indexed as

Abnormalities, Drug-InducedGabapentinPregabalinAdultCase-Control StudiesEuropeFemaleHumansPregnancyPregnancy Trimester, FirstRegistriesGabapentinPregabalin

Identifiers

PMID42230530
PMCPMC13498513

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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.