Evidence map›Paper›PMID 26819444›Full record

ArticleInternational journal of epidemiology2016

Application of linear mixed models to study genetic stability of height and body mass index across countries and time.

Maciej Trzaskowski, Paul Lichtenstein, Patrik K Magnusson, Nancy L Pedersen, Robert Plomin

Abstract read
In one paragraph

Article in International journal of epidemiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Maciej TrzaskowskiKing's College London, Institute of Psychiatry, Psychology & Neuroscience, London, UK and maciej.trzaskowski@kcl.ac.uk.
Paul LichtensteinKarolinska Institutet, Department of Medical Epidemiology and Biostatistics, Stockholm, Sweden.
Patrik K MagnussonKarolinska Institutet, Department of Medical Epidemiology and Biostatistics, Stockholm, Sweden.
Nancy L PedersenKarolinska Institutet, Department of Medical Epidemiology and Biostatistics, Stockholm, Sweden.
Robert PlominKing's College London, Institute of Psychiatry, Psychology & Neuroscience, London, UK and.

Funding

Genetics, School environments and cognitive developmentR01HD044454 · NICHD · KING'S COLLEGE LONDON · PI PLOMIN, ROBERT · 2005 to 2014
$3.4M
European Research Council 295366Medical Research Council G0500079Medical Research Council G0901245Medical Research Council G19/2NICHD NIH HHS R01 HD044454
6 · The paper itself

Abstract

backgroundIt is now possible to estimate genetic correlations between two independent samples when there is no overlapping phenotypic information. We applied the latest bivariate genomic methods to children in the UK and older adults in Sweden to ask two questions. Are the same variants driving individual differences in anthropometric traits in these two populations, and are these variants as important in childhood as they are later in life?

methodsA sample of 3152 11-year-old children in the UK was compared with a sample of 6813 adults with an average age of 65 in Sweden. Genotypes were imputed from 1000 genomes with combined 9 767 136 single nucleotide polymorphisms meeting quality control criteria in both samples. Two cross-sample GCTA-GREML analyses and linkage disequilibrium (LD) score regressions were conducted to assess genetic correlations across more than 50 years: child versus adult height and child versus adult body mass index (BMI). Consistency of effects was tested using the recently proposed polygenic scoring method.

resultsFor height, GCTA-GREML and LD score indicated strong genetic stability between children and adults, 0.58 (0.16) and 1.335 (1.09), respectively. For BMI, both methods produced similarly strong estimates of genetic stability 0.75 (0.26) and 0.855 (0.49), respectively. In height, adult polygenic score explained 60% of genetic variance in childhood and 10% of variance in BMI.

conclusionsHere we replicated and extended previous findings of longitudinal genetic stability in anthropometric traits to cross-cultural dimensions, and showed that for height but not BMI these variants are as important in childhood as they are in adulthood.

Indexed as

BMIGCTAgenetic stabilityGREMLheightLD score regressionpolygenic predictionUnrelated samplesweight

Identifiers

PMID26819444
PMCPMC4864877

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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.