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Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood
Neurocognitive abilities constitute complex traits with considerable heritability. Impaired neurocognition is typically observed in schizophrenia (SZ), whereas convergent evidence has shown shared genetic determinants between neurocognition and SZ. Here, we report a genome‐wide association study (GW...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008149/ https://www.ncbi.nlm.nih.gov/pubmed/25963331 http://dx.doi.org/10.1002/ajmg.b.32323 |
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author | Hatzimanolis, Alex Bhatnagar, Pallav Moes, Anna Wang, Ruihua Roussos, Panos Bitsios, Panos Stefanis, Costas N. Pulver, Ann E. Arking, Dan E. Smyrnis, Nikolaos Stefanis, Nicholas C. Avramopoulos, Dimitrios |
author_facet | Hatzimanolis, Alex Bhatnagar, Pallav Moes, Anna Wang, Ruihua Roussos, Panos Bitsios, Panos Stefanis, Costas N. Pulver, Ann E. Arking, Dan E. Smyrnis, Nikolaos Stefanis, Nicholas C. Avramopoulos, Dimitrios |
author_sort | Hatzimanolis, Alex |
collection | PubMed |
description | Neurocognitive abilities constitute complex traits with considerable heritability. Impaired neurocognition is typically observed in schizophrenia (SZ), whereas convergent evidence has shown shared genetic determinants between neurocognition and SZ. Here, we report a genome‐wide association study (GWAS) on neuropsychological and oculomotor traits, linked to SZ, in a general population sample of healthy young males (n = 1079). Follow‐up genotyping was performed in an identically phenotyped internal sample (n = 738) and an independent cohort of young males with comparable neuropsychological measures (n = 825). Heritability estimates were determined based on genome‐wide single‐nucleotide polymorphisms (SNPs) and potential regulatory effects on gene expression were assessed in human brain. Correlations with general cognitive ability and SZ risk polygenic scores were tested utilizing meta‐analysis GWAS results by the Cognitive Genomics Consortium (COGENT) and the Psychiatric Genomics Consortium (PGC‐SZ). The GWAS results implicated biologically relevant genetic loci encoding protein targets involved in synaptic neurotransmission, although no robust individual replication was detected and thus additional validation is required. Secondary permutation‐based analysis revealed an excess of strongly associated loci among GWAS top‐ranked signals for verbal working memory (WM) and antisaccade intra‐subject reaction time variability (empirical P < 0.001), suggesting multiple true‐positive single‐SNP associations. Substantial heritability was observed for WM performance. Further, sustained attention/vigilance and WM were suggestively correlated with both COGENT and PGC‐SZ derived polygenic scores. Overall, these results imply that common genetic variation explains some of the variability in neurocognitive functioning among young adults, particularly WM, and provide supportive evidence that increased SZ genetic risk predicts neurocognitive fluctuations in the general population. © 2015 The Authors American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-5008149 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50081492016-09-16 Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood Hatzimanolis, Alex Bhatnagar, Pallav Moes, Anna Wang, Ruihua Roussos, Panos Bitsios, Panos Stefanis, Costas N. Pulver, Ann E. Arking, Dan E. Smyrnis, Nikolaos Stefanis, Nicholas C. Avramopoulos, Dimitrios Am J Med Genet B Neuropsychiatr Genet Research Articles Neurocognitive abilities constitute complex traits with considerable heritability. Impaired neurocognition is typically observed in schizophrenia (SZ), whereas convergent evidence has shown shared genetic determinants between neurocognition and SZ. Here, we report a genome‐wide association study (GWAS) on neuropsychological and oculomotor traits, linked to SZ, in a general population sample of healthy young males (n = 1079). Follow‐up genotyping was performed in an identically phenotyped internal sample (n = 738) and an independent cohort of young males with comparable neuropsychological measures (n = 825). Heritability estimates were determined based on genome‐wide single‐nucleotide polymorphisms (SNPs) and potential regulatory effects on gene expression were assessed in human brain. Correlations with general cognitive ability and SZ risk polygenic scores were tested utilizing meta‐analysis GWAS results by the Cognitive Genomics Consortium (COGENT) and the Psychiatric Genomics Consortium (PGC‐SZ). The GWAS results implicated biologically relevant genetic loci encoding protein targets involved in synaptic neurotransmission, although no robust individual replication was detected and thus additional validation is required. Secondary permutation‐based analysis revealed an excess of strongly associated loci among GWAS top‐ranked signals for verbal working memory (WM) and antisaccade intra‐subject reaction time variability (empirical P < 0.001), suggesting multiple true‐positive single‐SNP associations. Substantial heritability was observed for WM performance. Further, sustained attention/vigilance and WM were suggestively correlated with both COGENT and PGC‐SZ derived polygenic scores. Overall, these results imply that common genetic variation explains some of the variability in neurocognitive functioning among young adults, particularly WM, and provide supportive evidence that increased SZ genetic risk predicts neurocognitive fluctuations in the general population. © 2015 The Authors American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2015-05-12 2015-07 /pmc/articles/PMC5008149/ /pubmed/25963331 http://dx.doi.org/10.1002/ajmg.b.32323 Text en © 2015 The Authors American Journal of Medical Genetics Part B: Neuropsychiatric Genetics Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Hatzimanolis, Alex Bhatnagar, Pallav Moes, Anna Wang, Ruihua Roussos, Panos Bitsios, Panos Stefanis, Costas N. Pulver, Ann E. Arking, Dan E. Smyrnis, Nikolaos Stefanis, Nicholas C. Avramopoulos, Dimitrios Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
title | Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
title_full | Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
title_fullStr | Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
title_full_unstemmed | Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
title_short | Common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
title_sort | common genetic variation and schizophrenia polygenic risk influence neurocognitive performance in young adulthood |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5008149/ https://www.ncbi.nlm.nih.gov/pubmed/25963331 http://dx.doi.org/10.1002/ajmg.b.32323 |
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