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dc.contributor.authorGiven, Joanne E.en_US
dc.contributor.authorLoane, Mariaen_US
dc.contributor.authorGarne, Esteren_US
dc.contributor.authorAddor, Marie-Claudeen_US
dc.contributor.authorBakker, Marianen_US
dc.contributor.authorBertaut-Nativel, Bénédicteen_US
dc.contributor.authorGatt, Miriamen_US
dc.contributor.authorKlungsøyr, Karien_US
dc.contributor.authorLelong, Nathalieen_US
dc.contributor.authorMorgan, Margeryen_US
dc.contributor.authorNeville, Amanda Jen_US
dc.contributor.authorPierini, Annaen_US
dc.contributor.authorRissmann, Ankeen_US
dc.contributor.authorDolk, Helenen_US
dc.date.accessioned2019-04-16T13:09:38Z
dc.date.available2019-04-16T13:09:38Z
dc.date.issued2018
dc.PublishedGiven JE, Loane M, Garne E, Addor M, Bakker M, Bertaut-Nativel, Gatt M, Klungsøyr K, Lelong N, Morgan M, Neville AJ, Pierini A, Rissmann A, Dolk H. Metformin exposure in first trimester of pregnancy and risk of all or specific congenital anomalies: exploratory case-control study. BMJ (Clinical Research Edition). 2018;361:k2477eng
dc.identifier.issn0959-8138
dc.identifier.urihttps://hdl.handle.net/1956/19369
dc.description.abstractObjective: To investigate whether exposure to metformin during the first trimester of pregnancy, for diabetes or other indications, increases the risk of all or specific congenital anomalies. Design: Population based exploratory case-control study using malformed controls. Cases of 29 specific subgroups of non-genetic anomalies, and all non-genetic anomalies combined, were compared with controls (all other non-genetic anomalies or genetic syndromes). Setting: 11 EUROmediCAT European congenital anomaly registries surveying 1 892 482 births in Europe between 2006 and 2013. Participants: 50 167 babies affected by congenital anomaly (41 242 non-genetic and 8925 genetic) including live births, fetal deaths from 20 weeks’ gestation, and terminations of pregnancy for fetal anomaly. Main outcome measure: Odds ratios adjusted for maternal age, registry, multiple birth, and maternal diabetes status. Results: 168 babies affected by congenital anomaly (141 non-genetic and 27 genetic) were exposed to metformin, 3.3 per 1000 births. No evidence was found for a higher proportion of exposure to metformin during the first trimester among babies with all non-genetic anomalies combined compared with genetic controls (adjusted odds ratio 0.84, 95% confidence interval 0.55 to 1.30). The only significant result was for pulmonary valve atresia (adjusted odds ratio 3.54, 1.05 to 12.00, compared with non-genetic controls; 2.86, 0.79 to 10.30, compared with genetic controls). Conclusions: No evidence was found for an increased risk of all non-genetic congenital anomalies combined following exposure to metformin during the first trimester, and the one significant association was no more than would be expected by chance. Further surveillance is needed to increase sample size and follow up the cardiac signal, but these findings are reassuring given the increasing use of metformin in pregnancy.en_US
dc.language.isoengeng
dc.publisherBMJeng
dc.relation.urihttps://www.bmj.com/content/bmj/361/bmj.k2477.full.pdf
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/4.0eng
dc.titleMetformin exposure in first trimester of pregnancy and risk of all or specific congenital anomalies: exploratory case-control studyen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2018-08-03T10:53:49Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2018 The Authors
dc.identifier.doihttps://doi.org/10.1136/bmj.k2477
dc.identifier.cristin1599621
dc.source.journalBMJ (Clinical Research Edition)


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