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Genetics of Callous-Unemotional Behavior in Children

Callous-unemotional behavior (CU) is currently under consideration as a subtyping index for conduct disorder diagnosis. Twin studies routinely estimate the heritability of CU as greater than 50%. It is now possible to estimate genetic influence using DNA alone from samples of unrelated individuals,...

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Autores principales: Viding, Essi, Price, Thomas S., Jaffee, Sara R., Trzaskowski, Maciej, Davis, Oliver S. P., Meaburn, Emma L., Haworth, Claire M. A., Plomin, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706442/
https://www.ncbi.nlm.nih.gov/pubmed/23874384
http://dx.doi.org/10.1371/journal.pone.0065789
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author Viding, Essi
Price, Thomas S.
Jaffee, Sara R.
Trzaskowski, Maciej
Davis, Oliver S. P.
Meaburn, Emma L.
Haworth, Claire M. A.
Plomin, Robert
author_facet Viding, Essi
Price, Thomas S.
Jaffee, Sara R.
Trzaskowski, Maciej
Davis, Oliver S. P.
Meaburn, Emma L.
Haworth, Claire M. A.
Plomin, Robert
author_sort Viding, Essi
collection PubMed
description Callous-unemotional behavior (CU) is currently under consideration as a subtyping index for conduct disorder diagnosis. Twin studies routinely estimate the heritability of CU as greater than 50%. It is now possible to estimate genetic influence using DNA alone from samples of unrelated individuals, not relying on the assumptions of the twin method. Here we use this new DNA method (implemented in a software package called Genome-wide Complex Trait Analysis, GCTA) for the first time to estimate genetic influence on CU. We also report the first genome-wide association (GWA) study of CU as a quantitative trait. We compare these DNA results to those from twin analyses using the same measure and the same community sample of 2,930 children rated by their teachers at ages 7, 9 and 12. GCTA estimates of heritability were near zero, even though twin analysis of CU in this sample confirmed the high heritability of CU reported in the literature, and even though GCTA estimates of heritability were substantial for cognitive and anthropological traits in this sample. No significant associations were found in GWA analysis, which, like GCTA, only detects additive effects of common DNA variants. The phrase ‘missing heritability’ was coined to refer to the gap between variance associated with DNA variants identified in GWA studies versus twin study heritability. However, GCTA heritability, not twin study heritability, is the ceiling for GWA studies because both GCTA and GWA are limited to the overall additive effects of common DNA variants, whereas twin studies are not. This GCTA ceiling is very low for CU in our study, despite its high twin study heritability estimate. The gap between GCTA and twin study heritabilities will make it challenging to identify genes responsible for the heritability of CU.
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spelling pubmed-37064422013-07-19 Genetics of Callous-Unemotional Behavior in Children Viding, Essi Price, Thomas S. Jaffee, Sara R. Trzaskowski, Maciej Davis, Oliver S. P. Meaburn, Emma L. Haworth, Claire M. A. Plomin, Robert PLoS One Research Article Callous-unemotional behavior (CU) is currently under consideration as a subtyping index for conduct disorder diagnosis. Twin studies routinely estimate the heritability of CU as greater than 50%. It is now possible to estimate genetic influence using DNA alone from samples of unrelated individuals, not relying on the assumptions of the twin method. Here we use this new DNA method (implemented in a software package called Genome-wide Complex Trait Analysis, GCTA) for the first time to estimate genetic influence on CU. We also report the first genome-wide association (GWA) study of CU as a quantitative trait. We compare these DNA results to those from twin analyses using the same measure and the same community sample of 2,930 children rated by their teachers at ages 7, 9 and 12. GCTA estimates of heritability were near zero, even though twin analysis of CU in this sample confirmed the high heritability of CU reported in the literature, and even though GCTA estimates of heritability were substantial for cognitive and anthropological traits in this sample. No significant associations were found in GWA analysis, which, like GCTA, only detects additive effects of common DNA variants. The phrase ‘missing heritability’ was coined to refer to the gap between variance associated with DNA variants identified in GWA studies versus twin study heritability. However, GCTA heritability, not twin study heritability, is the ceiling for GWA studies because both GCTA and GWA are limited to the overall additive effects of common DNA variants, whereas twin studies are not. This GCTA ceiling is very low for CU in our study, despite its high twin study heritability estimate. The gap between GCTA and twin study heritabilities will make it challenging to identify genes responsible for the heritability of CU. Public Library of Science 2013-07-09 /pmc/articles/PMC3706442/ /pubmed/23874384 http://dx.doi.org/10.1371/journal.pone.0065789 Text en © 2013 Viding et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Viding, Essi
Price, Thomas S.
Jaffee, Sara R.
Trzaskowski, Maciej
Davis, Oliver S. P.
Meaburn, Emma L.
Haworth, Claire M. A.
Plomin, Robert
Genetics of Callous-Unemotional Behavior in Children
title Genetics of Callous-Unemotional Behavior in Children
title_full Genetics of Callous-Unemotional Behavior in Children
title_fullStr Genetics of Callous-Unemotional Behavior in Children
title_full_unstemmed Genetics of Callous-Unemotional Behavior in Children
title_short Genetics of Callous-Unemotional Behavior in Children
title_sort genetics of callous-unemotional behavior in children
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3706442/
https://www.ncbi.nlm.nih.gov/pubmed/23874384
http://dx.doi.org/10.1371/journal.pone.0065789
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