A lifecourse mendelian randomization study highlights the long-term influence of childhood body size on later life heart structure
Children with obesity typically have larger left ventricular heart dimensions during adulthood. However, whether this is due to a persistent effect of adiposity extending into adulthood is challenging to disentangle due to confounding factors throughout the lifecourse. We conducted a multivariable m...
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description | Children with obesity typically have larger left ventricular heart dimensions during adulthood. However, whether this is due to a persistent effect of adiposity extending into adulthood is challenging to disentangle due to confounding factors throughout the lifecourse. We conducted a multivariable mendelian randomization (MR) study to separate the independent effects of childhood and adult body size on 4 magnetic resonance imaging (MRI) measures of heart structure and function in the UK Biobank (UKB) study. Strong evidence of a genetically predicted effect of childhood body size on all measures of adulthood heart structure was identified, which remained robust upon accounting for adult body size using a multivariable MR framework (e.g., left ventricular end-diastolic volume (LVEDV), Beta = 0.33, 95% confidence interval (CI) = 0.23 to 0.43, P = 4.6 × 10-10). Sensitivity analyses did not suggest that other lifecourse measures of body composition were responsible for these effects. Conversely, evidence of a genetically predicted effect of childhood body size on various other MRI-based measures, such as fat percentage in the liver (Beta = 0.14, 95% CI = 0.05 to 0.23, P = 0.002) and pancreas (Beta = 0.21, 95% CI = 0.10 to 0.33, P = 3.9 × 10-4), attenuated upon accounting for adult body size. Our findings suggest that childhood body size has a long-term (and potentially immutable) influence on heart structure in later life. In contrast, effects of childhood body size on other measures of adulthood organ size and fat percentage evaluated in this study are likely explained by the long-term consequence of remaining overweight throughout the lifecourse. |
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However, whether this is due to a persistent effect of adiposity extending into adulthood is challenging to disentangle due to confounding factors throughout the lifecourse. We conducted a multivariable mendelian randomization (MR) study to separate the independent effects of childhood and adult body size on 4 magnetic resonance imaging (MRI) measures of heart structure and function in the UK Biobank (UKB) study. Strong evidence of a genetically predicted effect of childhood body size on all measures of adulthood heart structure was identified, which remained robust upon accounting for adult body size using a multivariable MR framework (e.g., left ventricular end-diastolic volume (LVEDV), Beta = 0.33, 95% confidence interval (CI) = 0.23 to 0.43, P = 4.6 × 10-10). Sensitivity analyses did not suggest that other lifecourse measures of body composition were responsible for these effects. Conversely, evidence of a genetically predicted effect of childhood body size on various other MRI-based measures, such as fat percentage in the liver (Beta = 0.14, 95% CI = 0.05 to 0.23, P = 0.002) and pancreas (Beta = 0.21, 95% CI = 0.10 to 0.33, P = 3.9 × 10-4), attenuated upon accounting for adult body size. Our findings suggest that childhood body size has a long-term (and potentially immutable) influence on heart structure in later life. In contrast, effects of childhood body size on other measures of adulthood organ size and fat percentage evaluated in this study are likely explained by the long-term consequence of remaining overweight throughout the lifecourse.</description><identifier>ISSN: 1545-7885</identifier><identifier>ISSN: 1544-9173</identifier><identifier>EISSN: 1545-7885</identifier><identifier>DOI: 10.1371/journal.pbio.3001656</identifier><identifier>PMID: 35679339</identifier><language>eng</language><publisher>United States: Public Library of Science</publisher><subject>Abdomen ; Adipose tissue ; Adiposity - genetics ; Adult ; Adults ; Biology and Life Sciences ; Body composition ; Body fat ; Body Mass Index ; Body size ; Body Size - genetics ; Body weight ; Child ; Children ; Confidence intervals ; Discovery Report ; Genetic aspects ; Genome-Wide Association Study ; Health aspects ; Heart ; Humans ; Magnetic resonance imaging ; Medicine and Health Sciences ; Mendelian Randomization Analysis ; Obesity ; Overweight ; People and Places ; Physiological aspects ; Randomization ; Research and Analysis Methods ; Risk factors ; Sensitivity analysis ; Structure-function relationships ; Ventricle</subject><ispartof>PLoS biology, 2022-06, Vol.20 (6), p.e3001656</ispartof><rights>COPYRIGHT 2022 Public Library of Science</rights><rights>2022 O’Nunain et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. 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However, whether this is due to a persistent effect of adiposity extending into adulthood is challenging to disentangle due to confounding factors throughout the lifecourse. We conducted a multivariable mendelian randomization (MR) study to separate the independent effects of childhood and adult body size on 4 magnetic resonance imaging (MRI) measures of heart structure and function in the UK Biobank (UKB) study. Strong evidence of a genetically predicted effect of childhood body size on all measures of adulthood heart structure was identified, which remained robust upon accounting for adult body size using a multivariable MR framework (e.g., left ventricular end-diastolic volume (LVEDV), Beta = 0.33, 95% confidence interval (CI) = 0.23 to 0.43, P = 4.6 × 10-10). Sensitivity analyses did not suggest that other lifecourse measures of body composition were responsible for these effects. 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In contrast, effects of childhood body size on other measures of adulthood organ size and fat percentage evaluated in this study are likely explained by the long-term consequence of remaining overweight throughout the lifecourse.</description><subject>Abdomen</subject><subject>Adipose tissue</subject><subject>Adiposity - genetics</subject><subject>Adult</subject><subject>Adults</subject><subject>Biology and Life Sciences</subject><subject>Body composition</subject><subject>Body fat</subject><subject>Body Mass Index</subject><subject>Body size</subject><subject>Body Size - genetics</subject><subject>Body weight</subject><subject>Child</subject><subject>Children</subject><subject>Confidence intervals</subject><subject>Discovery Report</subject><subject>Genetic aspects</subject><subject>Genome-Wide Association Study</subject><subject>Health aspects</subject><subject>Heart</subject><subject>Humans</subject><subject>Magnetic resonance imaging</subject><subject>Medicine and Health Sciences</subject><subject>Mendelian Randomization Analysis</subject><subject>Obesity</subject><subject>Overweight</subject><subject>People and Places</subject><subject>Physiological aspects</subject><subject>Randomization</subject><subject>Research and Analysis Methods</subject><subject>Risk factors</subject><subject>Sensitivity analysis</subject><subject>Structure-function relationships</subject><subject>Ventricle</subject><issn>1545-7885</issn><issn>1544-9173</issn><issn>1545-7885</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>DOA</sourceid><recordid>eNqVk1trFDEUxwdRbK1-A9GAL_qway6Tyc6LUIqXQrHg7TXkcrKTkklqMiO2j35ys-22dMUHZQgTTn7__zk54TTNU4KXhAny-izNOaqwPNc-LRnGpOPdvWaf8JYvxGrF79_Z7zWPSjnDmNKerh42e4x3omes329-HaLgHZhqVgCNEC0EryLKKto0-ks1-RRRmWZ7gQa_HkJdU0HTACikuF5MkEfkowszRAMoOWQGH-yQkkU6VVHxlzUcUVAVvcqFBlB5qp55NtOc4XHzwKlQ4Mn2f9B8fff2y9GHxcnp--Ojw5OF6Xo-LXoiOGOO9xa0ppZxbARlBoQATRQlhugOrGadNlQLorV22GnhFKaMarDsoHl-7XseUpHb9hVJux4L2vLakIPm-JqwSZ3J8-xHlS9kUl5eBVJey1q5NwGk0yvXrjqKKe9b3JmeYGUdw20P1jLCq9ebbbZZj2ANxCmrsGO6exL9INfph-zJqpbEqsHLrUFO32cokxx9MRCCipDmTd2irR2hLa7oiz_Qv99uS61VvUB9s1Tzmo2pPBS450LwbkMt_0LVz8LoTYrgfI3vCF7tCCozwc9preZS5PHnT__Bfvx39vTbLttesyanUjK42z4TLDfTctMQuZkWuZ2WKnt2941uRTfjwX4D4WkSnw</recordid><startdate>20220609</startdate><enddate>20220609</enddate><creator>O'Nunain, Katie</creator><creator>Park, Chloe</creator><creator>Urquijo, Helena</creator><creator>Leyden, Genevieve M</creator><creator>Hughes, Alun D</creator><creator>Davey Smith, George</creator><creator>Richardson, Tom G</creator><general>Public Library of Science</general><general>Public Library of Science (PLoS)</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IOV</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>7QG</scope><scope>7QL</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PATMY</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PYCSY</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><scope>CZG</scope><orcidid>https://orcid.org/0000-0002-7918-2040</orcidid></search><sort><creationdate>20220609</creationdate><title>A lifecourse mendelian randomization study highlights the long-term influence of childhood body size on later life heart structure</title><author>O'Nunain, Katie ; Park, Chloe ; Urquijo, Helena ; Leyden, Genevieve M ; Hughes, Alun D ; Davey Smith, George ; Richardson, Tom G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c695t-917533f59debb2d350c723ce77eb1a21c1b6edb36bc2b71bbbf0fb7fa0232bed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Abdomen</topic><topic>Adipose tissue</topic><topic>Adiposity - 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However, whether this is due to a persistent effect of adiposity extending into adulthood is challenging to disentangle due to confounding factors throughout the lifecourse. We conducted a multivariable mendelian randomization (MR) study to separate the independent effects of childhood and adult body size on 4 magnetic resonance imaging (MRI) measures of heart structure and function in the UK Biobank (UKB) study. Strong evidence of a genetically predicted effect of childhood body size on all measures of adulthood heart structure was identified, which remained robust upon accounting for adult body size using a multivariable MR framework (e.g., left ventricular end-diastolic volume (LVEDV), Beta = 0.33, 95% confidence interval (CI) = 0.23 to 0.43, P = 4.6 × 10-10). Sensitivity analyses did not suggest that other lifecourse measures of body composition were responsible for these effects. Conversely, evidence of a genetically predicted effect of childhood body size on various other MRI-based measures, such as fat percentage in the liver (Beta = 0.14, 95% CI = 0.05 to 0.23, P = 0.002) and pancreas (Beta = 0.21, 95% CI = 0.10 to 0.33, P = 3.9 × 10-4), attenuated upon accounting for adult body size. Our findings suggest that childhood body size has a long-term (and potentially immutable) influence on heart structure in later life. In contrast, effects of childhood body size on other measures of adulthood organ size and fat percentage evaluated in this study are likely explained by the long-term consequence of remaining overweight throughout the lifecourse.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>35679339</pmid><doi>10.1371/journal.pbio.3001656</doi><orcidid>https://orcid.org/0000-0002-7918-2040</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Abdomen Adipose tissue Adiposity - genetics Adult Adults Biology and Life Sciences Body composition Body fat Body Mass Index Body size Body Size - genetics Body weight Child Children Confidence intervals Discovery Report Genetic aspects Genome-Wide Association Study Health aspects Heart Humans Magnetic resonance imaging Medicine and Health Sciences Mendelian Randomization Analysis Obesity Overweight People and Places Physiological aspects Randomization Research and Analysis Methods Risk factors Sensitivity analysis Structure-function relationships Ventricle |
title | A lifecourse mendelian randomization study highlights the long-term influence of childhood body size on later life heart structure |
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