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Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders
BACKGROUND: General cognitive function predicts psychiatric illness across the life course. This study examines the role of pleiotropy in explaining the link between cognitive function and psychiatric disorder. METHODS: We used two large genome-wide association study data sets on cognitive function—...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974237/ https://www.ncbi.nlm.nih.gov/pubmed/26476593 http://dx.doi.org/10.1016/j.biopsych.2015.08.033 |
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author | Hill, W. David Davies, Gail Liewald, David C. McIntosh, Andrew M. Deary, Ian J. |
author_facet | Hill, W. David Davies, Gail Liewald, David C. McIntosh, Andrew M. Deary, Ian J. |
author_sort | Hill, W. David |
collection | PubMed |
description | BACKGROUND: General cognitive function predicts psychiatric illness across the life course. This study examines the role of pleiotropy in explaining the link between cognitive function and psychiatric disorder. METHODS: We used two large genome-wide association study data sets on cognitive function—one from older age, n = 53,949, and one from childhood, n = 12,441. We also used genome-wide association study data on educational attainment, n = 95,427, to examine the validity of its use as a proxy phenotype for cognitive function. Using a new method, linkage disequilibrium regression, we derived genetic correlations, free from the confounding of clinical state between psychiatric illness and cognitive function. RESULTS: We found a genetic correlation of .711 (p = 2.26e-12) across the life course for general cognitive function. We also showed a positive genetic correlation between autism spectrum disorder and cognitive function in childhood (r(g) = .360, p = .0009) and for educational attainment (r(g) = .322, p = 1.37e-5) but not in older age. In schizophrenia, we found a negative genetic correlation between older age cognitive function (r(g) = −.231, p = 3.81e-12) but not in childhood or for educational attainment. For Alzheimer’s disease, we found negative genetic correlations with childhood cognitive function (r(g) = −.341, p = .001), educational attainment (r(g) = −.324, p = 1.15e-5), and with older age cognitive function (r(g) = −.324, p = 1.78e-5). CONCLUSIONS: The pleiotropy exhibited between cognitive function and psychiatric disorders changed across the life course. These age-dependent associations might explain why negative selection has not removed variants causally associated with autism spectrum disorder or schizophrenia. |
format | Online Article Text |
id | pubmed-4974237 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49742372016-08-15 Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders Hill, W. David Davies, Gail Liewald, David C. McIntosh, Andrew M. Deary, Ian J. Biol Psychiatry Priority Communication BACKGROUND: General cognitive function predicts psychiatric illness across the life course. This study examines the role of pleiotropy in explaining the link between cognitive function and psychiatric disorder. METHODS: We used two large genome-wide association study data sets on cognitive function—one from older age, n = 53,949, and one from childhood, n = 12,441. We also used genome-wide association study data on educational attainment, n = 95,427, to examine the validity of its use as a proxy phenotype for cognitive function. Using a new method, linkage disequilibrium regression, we derived genetic correlations, free from the confounding of clinical state between psychiatric illness and cognitive function. RESULTS: We found a genetic correlation of .711 (p = 2.26e-12) across the life course for general cognitive function. We also showed a positive genetic correlation between autism spectrum disorder and cognitive function in childhood (r(g) = .360, p = .0009) and for educational attainment (r(g) = .322, p = 1.37e-5) but not in older age. In schizophrenia, we found a negative genetic correlation between older age cognitive function (r(g) = −.231, p = 3.81e-12) but not in childhood or for educational attainment. For Alzheimer’s disease, we found negative genetic correlations with childhood cognitive function (r(g) = −.341, p = .001), educational attainment (r(g) = −.324, p = 1.15e-5), and with older age cognitive function (r(g) = −.324, p = 1.78e-5). CONCLUSIONS: The pleiotropy exhibited between cognitive function and psychiatric disorders changed across the life course. These age-dependent associations might explain why negative selection has not removed variants causally associated with autism spectrum disorder or schizophrenia. Elsevier 2016-08-15 /pmc/articles/PMC4974237/ /pubmed/26476593 http://dx.doi.org/10.1016/j.biopsych.2015.08.033 Text en © 2016 Society of Biological Psychiatry. All rights reserved. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Priority Communication Hill, W. David Davies, Gail Liewald, David C. McIntosh, Andrew M. Deary, Ian J. Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders |
title | Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders |
title_full | Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders |
title_fullStr | Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders |
title_full_unstemmed | Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders |
title_short | Age-Dependent Pleiotropy Between General Cognitive Function and Major Psychiatric Disorders |
title_sort | age-dependent pleiotropy between general cognitive function and major psychiatric disorders |
topic | Priority Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4974237/ https://www.ncbi.nlm.nih.gov/pubmed/26476593 http://dx.doi.org/10.1016/j.biopsych.2015.08.033 |
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