Evidence map›Paper›PMID 35679339›Full record

ArticlePLoS biology2022

A lifecourse mendelian randomization study highlights the long-term influence of childhood body size on later life heart structure.

Katie O'Nunain, Chloe Park, Helena Urquijo, Genevieve M Leyden, Alun D Hughes, George Davey Smith, Tom G Richardson

Abstract read
In one paragraph

Article in PLoS biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Katie O'NunainBristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom.
Chloe ParkMRC Unit for Lifelong Health and Ageing at UCL, Department of Population Science and Experimental Medicine, Institute of Cardiovascular Science, University College London, London, United Kingdom.
Helena UrquijoBristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom.
Genevieve M LeydenBristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom.
Alun D HughesMRC Unit for Lifelong Health and Ageing at UCL, Department of Population Science and Experimental Medicine, Institute of Cardiovascular Science, University College London, London, United Kingdom.
George Davey SmithBristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom.
Tom G RichardsonBristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol, United Kingdom.ORCID 0000-0002-7918-2040

Funding

British Heart Foundation CS/15/6/31468British Heart Foundation PG/06/145British Heart Foundation SP/F/21/150020Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_PC_17228Medical Research Council MC_PC_19009Medical Research Council MC_QA137853Medical Research Council MC_UU_00011/1Wellcome TrustWellcome Trust 086676/7/08/Z
6 · The paper itself

Abstract

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.

Indexed as

AdiposityMendelian Randomization AnalysisAdultBody Mass IndexBody SizeChildGenome-Wide Association StudyHumansObesity

Identifiers

PMID35679339
PMCPMC9182693

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.