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...

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Main Authors: Benjamin Woolf, Hannah M. Sallis, Marcus R. Munafò
Format: Article
Language:English
Published: MDPI AG 2023-03-01
Series:Genes
Subjects:
Online Access:https://www.mdpi.com/2073-4425/14/3/716
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author Benjamin Woolf
Hannah M. Sallis
Marcus R. Munafò
author_facet Benjamin Woolf
Hannah M. Sallis
Marcus R. Munafò
author_sort Benjamin Woolf
collection DOAJ
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.
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spelling doaj.art-cddbbacc47954e5186bcea02d0f7d0ee2023-11-17T11:18:27ZengMDPI AGGenes2073-44252023-03-0114371610.3390/genes14030716Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian RandomisationBenjamin Woolf0Hannah M. Sallis1Marcus R. Munafò2School of Psychological Science, University of Bristol, Bristol BS8 1TU, UKMRC Integrative Epidemiology Unit, University of Bristol, Bristol BS8 2BN, UKSchool of Psychological Science, University of Bristol, Bristol BS8 1TU, UKBackground: 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.https://www.mdpi.com/2073-4425/14/3/716Mendelian randomisationwellbeingfamily size
spellingShingle Benjamin Woolf
Hannah M. Sallis
Marcus R. Munafò
Exploring the Lifetime Effect of Children on Wellbeing Using Two-Sample Mendelian Randomisation
Genes
Mendelian randomisation
wellbeing
family size
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 Mendelian randomisation
wellbeing
family size
url https://www.mdpi.com/2073-4425/14/3/716
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