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The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study

BACKGROUND: Congenital heart diseases (CHDs) remain a significant cause of infant morbidity and mortality. Epidemiological studies have explored maternal risk factors for offspring CHDs, but few have used genetic epidemiology methods to improve causal inference. METHODS: Three birth cohorts, includi...

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Autores principales: Taylor, Kurt, Wootton, Robyn E., Yang, Qian, Oddie, Sam, Wright, John, Yang, Tiffany C., Magnus, Maria, Andreassen, Ole A., Borges, Maria Carolina, Caputo, Massimo, Lawlor, Deborah A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890815/
https://www.ncbi.nlm.nih.gov/pubmed/36721200
http://dx.doi.org/10.1186/s12916-023-02731-y
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author Taylor, Kurt
Wootton, Robyn E.
Yang, Qian
Oddie, Sam
Wright, John
Yang, Tiffany C.
Magnus, Maria
Andreassen, Ole A.
Borges, Maria Carolina
Caputo, Massimo
Lawlor, Deborah A.
author_facet Taylor, Kurt
Wootton, Robyn E.
Yang, Qian
Oddie, Sam
Wright, John
Yang, Tiffany C.
Magnus, Maria
Andreassen, Ole A.
Borges, Maria Carolina
Caputo, Massimo
Lawlor, Deborah A.
author_sort Taylor, Kurt
collection PubMed
description BACKGROUND: Congenital heart diseases (CHDs) remain a significant cause of infant morbidity and mortality. Epidemiological studies have explored maternal risk factors for offspring CHDs, but few have used genetic epidemiology methods to improve causal inference. METHODS: Three birth cohorts, including 65,510 mother/offspring pairs (N = 562 CHD cases) were included. We used Mendelian randomisation (MR) analyses to explore the effects of genetically predicted maternal body mass index (BMI), smoking and alcohol on offspring CHDs. We generated genetic risk scores (GRS) using summary data from large-scale genome-wide association studies (GWAS) and validated the strength and relevance of the genetic instrument for exposure levels during pregnancy. Logistic regression was used to estimate the odds ratio (OR) of CHD per 1 standard deviation (SD) higher GRS. Results for the three cohorts were combined using random-effects meta-analyses. We performed several sensitivity analyses including multivariable MR to check the robustness of our findings. RESULTS: The GRSs associated with the exposures during pregnancy in all three cohorts. The associations of the GRS for maternal BMI with offspring CHD (pooled OR (95% confidence interval) per 1SD higher GRS: 0.95 (0.88, 1.03)), lifetime smoking (pooled OR: 1.01 (0.93, 1.09)) and alcoholic drinks per week (pooled OR: 1.06 (0.98, 1.15)) were close to the null. Sensitivity analyses yielded similar results. CONCLUSIONS: Our results do not provide robust evidence of an effect of maternal BMI, smoking or alcohol on offspring CHDs. However, results were imprecise. Our findings need to be replicated, and highlight the need for more and larger studies with maternal and offspring genotype and offspring CHD data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02731-y.
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spelling pubmed-98908152023-02-02 The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study Taylor, Kurt Wootton, Robyn E. Yang, Qian Oddie, Sam Wright, John Yang, Tiffany C. Magnus, Maria Andreassen, Ole A. Borges, Maria Carolina Caputo, Massimo Lawlor, Deborah A. BMC Med Research Article BACKGROUND: Congenital heart diseases (CHDs) remain a significant cause of infant morbidity and mortality. Epidemiological studies have explored maternal risk factors for offspring CHDs, but few have used genetic epidemiology methods to improve causal inference. METHODS: Three birth cohorts, including 65,510 mother/offspring pairs (N = 562 CHD cases) were included. We used Mendelian randomisation (MR) analyses to explore the effects of genetically predicted maternal body mass index (BMI), smoking and alcohol on offspring CHDs. We generated genetic risk scores (GRS) using summary data from large-scale genome-wide association studies (GWAS) and validated the strength and relevance of the genetic instrument for exposure levels during pregnancy. Logistic regression was used to estimate the odds ratio (OR) of CHD per 1 standard deviation (SD) higher GRS. Results for the three cohorts were combined using random-effects meta-analyses. We performed several sensitivity analyses including multivariable MR to check the robustness of our findings. RESULTS: The GRSs associated with the exposures during pregnancy in all three cohorts. The associations of the GRS for maternal BMI with offspring CHD (pooled OR (95% confidence interval) per 1SD higher GRS: 0.95 (0.88, 1.03)), lifetime smoking (pooled OR: 1.01 (0.93, 1.09)) and alcoholic drinks per week (pooled OR: 1.06 (0.98, 1.15)) were close to the null. Sensitivity analyses yielded similar results. CONCLUSIONS: Our results do not provide robust evidence of an effect of maternal BMI, smoking or alcohol on offspring CHDs. However, results were imprecise. Our findings need to be replicated, and highlight the need for more and larger studies with maternal and offspring genotype and offspring CHD data. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12916-023-02731-y. BioMed Central 2023-02-01 /pmc/articles/PMC9890815/ /pubmed/36721200 http://dx.doi.org/10.1186/s12916-023-02731-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Taylor, Kurt
Wootton, Robyn E.
Yang, Qian
Oddie, Sam
Wright, John
Yang, Tiffany C.
Magnus, Maria
Andreassen, Ole A.
Borges, Maria Carolina
Caputo, Massimo
Lawlor, Deborah A.
The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study
title The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study
title_full The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study
title_fullStr The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study
title_full_unstemmed The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study
title_short The effect of maternal BMI, smoking and alcohol on congenital heart diseases: a Mendelian randomisation study
title_sort effect of maternal bmi, smoking and alcohol on congenital heart diseases: a mendelian randomisation study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9890815/
https://www.ncbi.nlm.nih.gov/pubmed/36721200
http://dx.doi.org/10.1186/s12916-023-02731-y
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