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A population-based matched cohort study of major congenital anomalies following COVID-19 vaccination and SARS-CoV-2 infection.

Calvert, C; Carruthers, J; Denny, C; Donaghy, J; Hopcroft, LEM; Hopkins, L; Goulding, A; Lindsay, L; McLaughlin, T; Moore, E; et al. Calvert, C; Carruthers, J; Denny, C; Donaghy, J; Hopcroft, LEM; Hopkins, L; Goulding, A; Lindsay, L; McLaughlin, T; Moore, E; Taylor, B; Loane, M; Dolk, H; Morris, J; Auyeung, B; Bhaskaran, K; Gibbons, CL; Katikireddi, SV; O'Leary, M; McAllister, D; Shi, T; Simpson, CR; Robertson, C; Sheikh, A; Stock, SJ; Wood, R (2023) A population-based matched cohort study of major congenital anomalies following COVID-19 vaccination and SARS-CoV-2 infection. Nat Commun, 14 (1). p. 107. ISSN 2041-1723 https://doi.org/10.1038/s41467-022-35771-8
SGUL Authors: Morris, Joan Katherine

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Abstract

Evidence on associations between COVID-19 vaccination or SARS-CoV-2 infection and the risk of congenital anomalies is limited. Here we report a national, population-based, matched cohort study using linked electronic health records from Scotland (May 2020-April 2022) to estimate the association between COVID-19 vaccination and, separately, SARS-CoV-2 infection between six weeks pre-conception and 19 weeks and six days gestation and the risk of [1] any major congenital anomaly and [2] any non-genetic major congenital anomaly. Mothers vaccinated in this pregnancy exposure period mostly received an mRNA vaccine (73.7% Pfizer-BioNTech BNT162b2 and 7.9% Moderna mRNA-1273). Of the 6731 babies whose mothers were vaccinated in the pregnancy exposure period, 153 had any anomaly and 120 had a non-genetic anomaly. Primary analyses find no association between any vaccination and any anomaly (adjusted Odds Ratio [aOR] = 1.01, 95% Confidence Interval [CI] = 0.83-1.24) or non-genetic anomalies (aOR = 1.00, 95% CI = 0.81-1.22). Primary analyses also find no association between SARS-CoV-2 infection and any anomaly (aOR = 1.02, 95% CI = 0.66-1.60) or non-genetic anomalies (aOR = 0.94, 95% CI = 0.57-1.54). Findings are robust to sensitivity analyses. These data provide reassurance on the safety of vaccination, in particular mRNA vaccines, just before or in early pregnancy.

Item Type: Article
Additional Information: Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. © The Author(s) 2023
Keywords: Female, Humans, Pregnancy, BNT162 Vaccine, Cohort Studies, COVID-19, COVID-19 Vaccines, SARS-CoV-2, Vaccination, Humans, Vaccination, Cohort Studies, Pregnancy, Female, COVID-19, SARS-CoV-2, COVID-19 Vaccines, BNT162 Vaccine
SGUL Research Institute / Research Centre: Academic Structure > Population Health Research Institute (INPH)
Journal or Publication Title: Nat Commun
ISSN: 2041-1723
Language: eng
Dates:
DateEvent
6 January 2023Published
22 December 2022Accepted
Publisher License: Creative Commons: Attribution 4.0
Projects:
Project IDFunderFunder ID
MC_PC_19075Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
MC_PC_19004Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
209560/Z/17/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
SCAF/15/02NHS Research ScotlandUNSPECIFIED
MC_UU_00022/2Medical Research Councilhttp://dx.doi.org/10.13039/501100000265
SPHSU17Chief Scientist Officehttp://dx.doi.org/10.13039/501100000589
220283/Z/20/ZWellcome Trusthttp://dx.doi.org/10.13039/100004440
PubMed ID: 36609574
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/115140
Publisher's version: https://doi.org/10.1038/s41467-022-35771-8

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