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A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions

Many psychiatric and neurodevelopmental disorders are known to be heritable, but studies trying to elucidate the genetic architecture of such traits often lag behind studies of somatic traits and diseases. The reasons as to why relatively few genome-wide significant associations have been reported f...

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Autores principales: Nudel, Ron, Zetterberg, Richard, Hemager, Nicoline, Christiani, Camilla A. J., Ohland, Jessica, Burton, Birgitte K., Greve, Aja N., Spang, Katrine S., Ellersgaard, Ditte, Gantriis, Ditte L., Bybjerg-Grauholm, Jonas, Plessen, Kerstin J., Jepsen, Jens Richardt M., Thorup, Anne A. E., Werge, Thomas, Mors, Ole, Nordentoft, Merete
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714039/
https://www.ncbi.nlm.nih.gov/pubmed/36457050
http://dx.doi.org/10.1186/s12993-022-00198-0
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author Nudel, Ron
Zetterberg, Richard
Hemager, Nicoline
Christiani, Camilla A. J.
Ohland, Jessica
Burton, Birgitte K.
Greve, Aja N.
Spang, Katrine S.
Ellersgaard, Ditte
Gantriis, Ditte L.
Bybjerg-Grauholm, Jonas
Plessen, Kerstin J.
Jepsen, Jens Richardt M.
Thorup, Anne A. E.
Werge, Thomas
Mors, Ole
Nordentoft, Merete
author_facet Nudel, Ron
Zetterberg, Richard
Hemager, Nicoline
Christiani, Camilla A. J.
Ohland, Jessica
Burton, Birgitte K.
Greve, Aja N.
Spang, Katrine S.
Ellersgaard, Ditte
Gantriis, Ditte L.
Bybjerg-Grauholm, Jonas
Plessen, Kerstin J.
Jepsen, Jens Richardt M.
Thorup, Anne A. E.
Werge, Thomas
Mors, Ole
Nordentoft, Merete
author_sort Nudel, Ron
collection PubMed
description Many psychiatric and neurodevelopmental disorders are known to be heritable, but studies trying to elucidate the genetic architecture of such traits often lag behind studies of somatic traits and diseases. The reasons as to why relatively few genome-wide significant associations have been reported for such traits have to do with the sample sizes needed for the detection of small effects, the difficulty in defining and characterizing the phenotypes, partially due to overlaps in affected underlying domains (which is especially true for cognitive phenotypes), and the complex genetic architectures of the phenotypes, which are not wholly captured in traditional case–control GWAS designs. We aimed to tackle the last two issues by performing GWASs of eight quantitative neurocognitive, motor, social-cognitive and social-behavioral traits, which may be considered endophenotypes for a variety of psychiatric and neurodevelopmental conditions, and for which we employed models capturing both general genetic association and parent-of-origin effects, in a family-based sample comprising 402 children and their parents (mostly family trios). We identified 48 genome-wide significant associations across several traits, of which 3 also survived our strict study-wide quality criteria. We additionally performed a functional annotation of implicated genes, as most of the 48 associations were with variants within protein-coding genes. In total, our study highlighted associations with five genes (TGM3, CACNB4, ANKS1B, CSMD1 and SYNE1) associated with measures of working memory, processing speed and social behavior. Our results thus identify novel associations, including previously unreported parent-of-origin associations with relevant genes, and our top results illustrate new potential gene → endophenotype → disorder pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12993-022-00198-0.
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spelling pubmed-97140392022-12-02 A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions Nudel, Ron Zetterberg, Richard Hemager, Nicoline Christiani, Camilla A. J. Ohland, Jessica Burton, Birgitte K. Greve, Aja N. Spang, Katrine S. Ellersgaard, Ditte Gantriis, Ditte L. Bybjerg-Grauholm, Jonas Plessen, Kerstin J. Jepsen, Jens Richardt M. Thorup, Anne A. E. Werge, Thomas Mors, Ole Nordentoft, Merete Behav Brain Funct Research Many psychiatric and neurodevelopmental disorders are known to be heritable, but studies trying to elucidate the genetic architecture of such traits often lag behind studies of somatic traits and diseases. The reasons as to why relatively few genome-wide significant associations have been reported for such traits have to do with the sample sizes needed for the detection of small effects, the difficulty in defining and characterizing the phenotypes, partially due to overlaps in affected underlying domains (which is especially true for cognitive phenotypes), and the complex genetic architectures of the phenotypes, which are not wholly captured in traditional case–control GWAS designs. We aimed to tackle the last two issues by performing GWASs of eight quantitative neurocognitive, motor, social-cognitive and social-behavioral traits, which may be considered endophenotypes for a variety of psychiatric and neurodevelopmental conditions, and for which we employed models capturing both general genetic association and parent-of-origin effects, in a family-based sample comprising 402 children and their parents (mostly family trios). We identified 48 genome-wide significant associations across several traits, of which 3 also survived our strict study-wide quality criteria. We additionally performed a functional annotation of implicated genes, as most of the 48 associations were with variants within protein-coding genes. In total, our study highlighted associations with five genes (TGM3, CACNB4, ANKS1B, CSMD1 and SYNE1) associated with measures of working memory, processing speed and social behavior. Our results thus identify novel associations, including previously unreported parent-of-origin associations with relevant genes, and our top results illustrate new potential gene → endophenotype → disorder pathways. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12993-022-00198-0. BioMed Central 2022-12-01 /pmc/articles/PMC9714039/ /pubmed/36457050 http://dx.doi.org/10.1186/s12993-022-00198-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Nudel, Ron
Zetterberg, Richard
Hemager, Nicoline
Christiani, Camilla A. J.
Ohland, Jessica
Burton, Birgitte K.
Greve, Aja N.
Spang, Katrine S.
Ellersgaard, Ditte
Gantriis, Ditte L.
Bybjerg-Grauholm, Jonas
Plessen, Kerstin J.
Jepsen, Jens Richardt M.
Thorup, Anne A. E.
Werge, Thomas
Mors, Ole
Nordentoft, Merete
A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
title A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
title_full A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
title_fullStr A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
title_full_unstemmed A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
title_short A family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
title_sort family-based study of genetic and epigenetic effects across multiple neurocognitive, motor, social-cognitive and social-behavioral functions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714039/
https://www.ncbi.nlm.nih.gov/pubmed/36457050
http://dx.doi.org/10.1186/s12993-022-00198-0
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