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Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank

A variety of statistical approaches in nutritional epidemiology have been developed to enhance the precision of dietary variables derived from longitudinal questionnaires. Correlation with biomarkers is often used to assess the relative validity of these different approaches, however, validated biom...

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Autores principales: Cole, Joanne B., Westerman, Kenneth E., Manning, Alisa K., Florez, Jose C., Hirschhorn, Joel N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845390/
https://www.ncbi.nlm.nih.gov/pubmed/36685884
http://dx.doi.org/10.3389/fgene.2022.1070511
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author Cole, Joanne B.
Westerman, Kenneth E.
Manning, Alisa K.
Florez, Jose C.
Hirschhorn, Joel N.
author_facet Cole, Joanne B.
Westerman, Kenneth E.
Manning, Alisa K.
Florez, Jose C.
Hirschhorn, Joel N.
author_sort Cole, Joanne B.
collection PubMed
description A variety of statistical approaches in nutritional epidemiology have been developed to enhance the precision of dietary variables derived from longitudinal questionnaires. Correlation with biomarkers is often used to assess the relative validity of these different approaches, however, validated biomarkers do not always exist and are costly and laborious to collect. We present a novel high-throughput approach which utilizes the modest but importantly non-zero influence of genetic variation on variation in dietary intake to compare different statistical transformations of dietary variables. Specifically, we compare the heritability of crude averages with Empirical Bayes weighted averages for 302 correlated dietary variables from multiple 24-hour recall questionnaires in 177 K individuals in UK Biobank. Overall, the crude averages for frequency of consumption are more heritable than their Empirical Bayes counterparts only when the reliability of that item across questionnaires is high (measured by intra-class correlation), otherwise, the Empirical Bayes approach (for both unreliably measured frequencies and for average quantities independent of reliability) leads to higher heritability estimates. We also find that the more heritable versions of each dietary variable lead to stronger underlying statistical associations with specific genetic loci, many of which have well-known mechanisms, further supporting heritability as an alternative metric for relative validity in nutritional epidemiology and beyond.
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spelling pubmed-98453902023-01-19 Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank Cole, Joanne B. Westerman, Kenneth E. Manning, Alisa K. Florez, Jose C. Hirschhorn, Joel N. Front Genet Genetics A variety of statistical approaches in nutritional epidemiology have been developed to enhance the precision of dietary variables derived from longitudinal questionnaires. Correlation with biomarkers is often used to assess the relative validity of these different approaches, however, validated biomarkers do not always exist and are costly and laborious to collect. We present a novel high-throughput approach which utilizes the modest but importantly non-zero influence of genetic variation on variation in dietary intake to compare different statistical transformations of dietary variables. Specifically, we compare the heritability of crude averages with Empirical Bayes weighted averages for 302 correlated dietary variables from multiple 24-hour recall questionnaires in 177 K individuals in UK Biobank. Overall, the crude averages for frequency of consumption are more heritable than their Empirical Bayes counterparts only when the reliability of that item across questionnaires is high (measured by intra-class correlation), otherwise, the Empirical Bayes approach (for both unreliably measured frequencies and for average quantities independent of reliability) leads to higher heritability estimates. We also find that the more heritable versions of each dietary variable lead to stronger underlying statistical associations with specific genetic loci, many of which have well-known mechanisms, further supporting heritability as an alternative metric for relative validity in nutritional epidemiology and beyond. Frontiers Media S.A. 2023-01-04 /pmc/articles/PMC9845390/ /pubmed/36685884 http://dx.doi.org/10.3389/fgene.2022.1070511 Text en Copyright © 2023 Cole, Westerman, Manning, Florez and Hirschhorn. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Cole, Joanne B.
Westerman, Kenneth E.
Manning, Alisa K.
Florez, Jose C.
Hirschhorn, Joel N.
Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank
title Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank
title_full Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank
title_fullStr Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank
title_full_unstemmed Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank
title_short Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank
title_sort genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in uk biobank
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9845390/
https://www.ncbi.nlm.nih.gov/pubmed/36685884
http://dx.doi.org/10.3389/fgene.2022.1070511
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