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Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation
Background: Observational research implies a negative effect of having children on wellbeing. Objectives: To provide Mendelian randomisation evidence of the effect of having children on parental wellbeing. Design: Two-sample Mendelian randomisation. Setting: Non-clinical European ancestry participan...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048211/ https://www.ncbi.nlm.nih.gov/pubmed/36980988 http://dx.doi.org/10.3390/genes14030716 |
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author | Woolf, Benjamin Sallis, Hannah M. Munafò, Marcus R. |
author_facet | Woolf, Benjamin Sallis, Hannah M. Munafò, Marcus R. |
author_sort | Woolf, Benjamin |
collection | PubMed |
description | Background: Observational research implies a negative effect of having children on wellbeing. Objectives: To provide Mendelian randomisation evidence of the effect of having children on parental wellbeing. Design: Two-sample Mendelian randomisation. Setting: Non-clinical European ancestry participants. Participants: We used the UK Biobank (460,654 male and female European ancestry participants) as a source of genotype-exposure associations, the Social Science Genetics Consortia (SSGAC) (298,420 male and female European ancestry participants), and the Within-Family Consortia (effective sample of 22,656 male and female European ancestry participants) as sources of genotype-outcome associations. Interventions: The lifetime effect of an increase in the genetic liability to having children. Primary and secondary outcome measures: The primary analysis was an inverse variance weighed analysis of subjective wellbeing measured in the 2016 SSGAC Genome Wide Association Study (GWAS). Secondary outcomes included pleiotropy robust estimators applied in the SSGAC and an analysis using the Within-Family consortia GWAS. Results: We did not find strong evidence of a negative (standard deviation) change in wellbeing (β = 0.153 (95% CI: −0.210 to 0.516) per child parented. Secondary outcomes were generally slightly deflated (e.g., −0.049 [95% CI: −0.533 to 0.435] for the Within-Family Consortia and 0.090 [95% CI: −0.167 to 0.347] for weighted median), implying the presence of some residual confounding and pleiotropy. Conclusions: Contrary to the existing literature, our results are not compatible with a measurable negative effect of number of children on the average wellbeing of a parent over their life course. However, we were unable to explore non-linearities, interactions, or time-varying effects. |
format | Online Article Text |
id | pubmed-10048211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-100482112023-03-29 Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation Woolf, Benjamin Sallis, Hannah M. Munafò, Marcus R. Genes (Basel) Article Background: Observational research implies a negative effect of having children on wellbeing. Objectives: To provide Mendelian randomisation evidence of the effect of having children on parental wellbeing. Design: Two-sample Mendelian randomisation. Setting: Non-clinical European ancestry participants. Participants: We used the UK Biobank (460,654 male and female European ancestry participants) as a source of genotype-exposure associations, the Social Science Genetics Consortia (SSGAC) (298,420 male and female European ancestry participants), and the Within-Family Consortia (effective sample of 22,656 male and female European ancestry participants) as sources of genotype-outcome associations. Interventions: The lifetime effect of an increase in the genetic liability to having children. Primary and secondary outcome measures: The primary analysis was an inverse variance weighed analysis of subjective wellbeing measured in the 2016 SSGAC Genome Wide Association Study (GWAS). Secondary outcomes included pleiotropy robust estimators applied in the SSGAC and an analysis using the Within-Family consortia GWAS. Results: We did not find strong evidence of a negative (standard deviation) change in wellbeing (β = 0.153 (95% CI: −0.210 to 0.516) per child parented. Secondary outcomes were generally slightly deflated (e.g., −0.049 [95% CI: −0.533 to 0.435] for the Within-Family Consortia and 0.090 [95% CI: −0.167 to 0.347] for weighted median), implying the presence of some residual confounding and pleiotropy. Conclusions: Contrary to the existing literature, our results are not compatible with a measurable negative effect of number of children on the average wellbeing of a parent over their life course. However, we were unable to explore non-linearities, interactions, or time-varying effects. MDPI 2023-03-14 /pmc/articles/PMC10048211/ /pubmed/36980988 http://dx.doi.org/10.3390/genes14030716 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Woolf, Benjamin Sallis, Hannah M. Munafò, Marcus R. Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation |
title | Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation |
title_full | Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation |
title_fullStr | Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation |
title_full_unstemmed | Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation |
title_short | Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation |
title_sort | exploring the lifetime effect of children on wellbeing using two-sample mendelian randomisation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10048211/ https://www.ncbi.nlm.nih.gov/pubmed/36980988 http://dx.doi.org/10.3390/genes14030716 |
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