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Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population

Epilepsy is clinically heterogeneous, and neurological or psychiatric comorbidities are frequently observed in patients. It has not been tested whether common risk variants for generalized or focal epilepsy are enriched in people with other disorders or traits related to brain or cognitive function....

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Autores principales: Leu, Costin, Richardson, Tom G., Kaufmann, Tobias, van der Meer, Dennis, Andreassen, Ole A., Westlye, Lars T., Busch, Robyn M., Davey Smith, George, Lal, Dennis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188256/
https://www.ncbi.nlm.nih.gov/pubmed/32343744
http://dx.doi.org/10.1371/journal.pone.0232292
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author Leu, Costin
Richardson, Tom G.
Kaufmann, Tobias
van der Meer, Dennis
Andreassen, Ole A.
Westlye, Lars T.
Busch, Robyn M.
Davey Smith, George
Lal, Dennis
author_facet Leu, Costin
Richardson, Tom G.
Kaufmann, Tobias
van der Meer, Dennis
Andreassen, Ole A.
Westlye, Lars T.
Busch, Robyn M.
Davey Smith, George
Lal, Dennis
author_sort Leu, Costin
collection PubMed
description Epilepsy is clinically heterogeneous, and neurological or psychiatric comorbidities are frequently observed in patients. It has not been tested whether common risk variants for generalized or focal epilepsy are enriched in people with other disorders or traits related to brain or cognitive function. Here, we perform two brain-focused phenome association studies of polygenic risk scores (PRS) for generalized epilepsy (GE-PRS) or focal epilepsy (FE-PRS) with all binary brain or cognitive function-related traits available for 334,310 European-ancestry individuals of the UK Biobank. Higher GE-PRS were associated with not having a college or university degree (P = 3.00x10(-4)), five neuroticism-related personality traits (P<2.51x10(-4)), and having ever smoked (P = 1.27x10(-6)). Higher FE-PRS were associated with several measures of low educational attainment (P<4.87x10(-5)), one neuroticism-related personality trait (P = 2.33x10(-4)), having ever smoked (P = 1.71x10(-4)), and having experienced events of anxiety or depression (P = 2.83x10(-4)). GE- and FE-PRS had the same direction of effect for each of the associated traits. Genetic factors associated with GE or FE showed similar patterns of correlation with genetic factors associated with cortical morphology in a subset of the UKB with 16,612 individuals and T1 magnetic resonance imaging data. In summary, our results suggest that genetic factors associated with epilepsies may confer risk for other neurological and psychiatric disorders in a population sample not enriched for epilepsy.
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spelling pubmed-71882562020-05-06 Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population Leu, Costin Richardson, Tom G. Kaufmann, Tobias van der Meer, Dennis Andreassen, Ole A. Westlye, Lars T. Busch, Robyn M. Davey Smith, George Lal, Dennis PLoS One Research Article Epilepsy is clinically heterogeneous, and neurological or psychiatric comorbidities are frequently observed in patients. It has not been tested whether common risk variants for generalized or focal epilepsy are enriched in people with other disorders or traits related to brain or cognitive function. Here, we perform two brain-focused phenome association studies of polygenic risk scores (PRS) for generalized epilepsy (GE-PRS) or focal epilepsy (FE-PRS) with all binary brain or cognitive function-related traits available for 334,310 European-ancestry individuals of the UK Biobank. Higher GE-PRS were associated with not having a college or university degree (P = 3.00x10(-4)), five neuroticism-related personality traits (P<2.51x10(-4)), and having ever smoked (P = 1.27x10(-6)). Higher FE-PRS were associated with several measures of low educational attainment (P<4.87x10(-5)), one neuroticism-related personality trait (P = 2.33x10(-4)), having ever smoked (P = 1.71x10(-4)), and having experienced events of anxiety or depression (P = 2.83x10(-4)). GE- and FE-PRS had the same direction of effect for each of the associated traits. Genetic factors associated with GE or FE showed similar patterns of correlation with genetic factors associated with cortical morphology in a subset of the UKB with 16,612 individuals and T1 magnetic resonance imaging data. In summary, our results suggest that genetic factors associated with epilepsies may confer risk for other neurological and psychiatric disorders in a population sample not enriched for epilepsy. Public Library of Science 2020-04-28 /pmc/articles/PMC7188256/ /pubmed/32343744 http://dx.doi.org/10.1371/journal.pone.0232292 Text en © 2020 Leu 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Leu, Costin
Richardson, Tom G.
Kaufmann, Tobias
van der Meer, Dennis
Andreassen, Ole A.
Westlye, Lars T.
Busch, Robyn M.
Davey Smith, George
Lal, Dennis
Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population
title Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population
title_full Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population
title_fullStr Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population
title_full_unstemmed Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population
title_short Pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population
title_sort pleiotropy of polygenic factors associated with focal and generalized epilepsy in the general population
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188256/
https://www.ncbi.nlm.nih.gov/pubmed/32343744
http://dx.doi.org/10.1371/journal.pone.0232292
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