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Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects
Objective: Various measures of neurocognitive function show mean differences among individuals with schizophrenia (SZ), their relatives, and population controls. We use eigenvector transformations that maximize heritability of multiple neurocognitive measures, namely principal components of heritabi...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576168/ https://www.ncbi.nlm.nih.gov/pubmed/22234486 http://dx.doi.org/10.1093/schbul/sbr161 |
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author | Wiener, Howard Klei, Lambertus Calkins, Monica Wood, Joel Nimgaonkar, Vishwajit Gur, Ruben Bradford, L. DiAnne Richard, Jan Edwards, Neil Savage, Robert Kwentus, Joseph Allen, Trina McEvoy, Joseph Santos, Alberto Gur, Raquel Devlin, Bernie Go, Rodney |
author_facet | Wiener, Howard Klei, Lambertus Calkins, Monica Wood, Joel Nimgaonkar, Vishwajit Gur, Ruben Bradford, L. DiAnne Richard, Jan Edwards, Neil Savage, Robert Kwentus, Joseph Allen, Trina McEvoy, Joseph Santos, Alberto Gur, Raquel Devlin, Bernie Go, Rodney |
author_sort | Wiener, Howard |
collection | PubMed |
description | Objective: Various measures of neurocognitive function show mean differences among individuals with schizophrenia (SZ), their relatives, and population controls. We use eigenvector transformations that maximize heritability of multiple neurocognitive measures, namely principal components of heritability (PCH), and evaluate how they distribute in SZ families and controls. Methods: African-Americans with SZ or schizoaffective disorder (SZA) (n = 514), their relatives (n = 1092), and adult controls (n = 300) completed diagnostic interviews and computerized neurocognitive tests. PCH were estimated from 9 neurocognitive domains. Three PCH, PCH1–PCH3, were modeled to determine if status (SZ, relative, and control), other psychiatric covariates, and education were significant predictors of mean values. A small-scale linkage analysis was also conducted in a subset of the sample. Results: PCH1, PCH2, and PCH3 account for 72% of the genetic variance. PCH1 represents 8 of 9 neurocognitive domains, is most highly correlated with spatial processing and emotion recognition, and has unadjusted heritability of 68%. The means for PCH1 differ significantly among SZ, their relatives, and controls. PCH2, orthogonal to PCH1, is most closely correlated with working memory and has an unadjusted heritability of 45%. Mean PCH2 is different only between SZ families and controls. PCH3 apparently represents a heritable component of neurocognition similar across the 3 diagnostic groups. No significant linkage evidence to PCH1–PCH3 or individual neurocognitive measures was discovered. Conclusions: PCH1 is highly heritable and genetically correlated with SZ. It should prove useful in future genetic analyses. Mean PCH2 differentiates SZ families and controls but not SZ and unaffected family members. |
format | Online Article Text |
id | pubmed-3576168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-35761682013-02-20 Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects Wiener, Howard Klei, Lambertus Calkins, Monica Wood, Joel Nimgaonkar, Vishwajit Gur, Ruben Bradford, L. DiAnne Richard, Jan Edwards, Neil Savage, Robert Kwentus, Joseph Allen, Trina McEvoy, Joseph Santos, Alberto Gur, Raquel Devlin, Bernie Go, Rodney Schizophr Bull Regular Article Objective: Various measures of neurocognitive function show mean differences among individuals with schizophrenia (SZ), their relatives, and population controls. We use eigenvector transformations that maximize heritability of multiple neurocognitive measures, namely principal components of heritability (PCH), and evaluate how they distribute in SZ families and controls. Methods: African-Americans with SZ or schizoaffective disorder (SZA) (n = 514), their relatives (n = 1092), and adult controls (n = 300) completed diagnostic interviews and computerized neurocognitive tests. PCH were estimated from 9 neurocognitive domains. Three PCH, PCH1–PCH3, were modeled to determine if status (SZ, relative, and control), other psychiatric covariates, and education were significant predictors of mean values. A small-scale linkage analysis was also conducted in a subset of the sample. Results: PCH1, PCH2, and PCH3 account for 72% of the genetic variance. PCH1 represents 8 of 9 neurocognitive domains, is most highly correlated with spatial processing and emotion recognition, and has unadjusted heritability of 68%. The means for PCH1 differ significantly among SZ, their relatives, and controls. PCH2, orthogonal to PCH1, is most closely correlated with working memory and has an unadjusted heritability of 45%. Mean PCH2 is different only between SZ families and controls. PCH3 apparently represents a heritable component of neurocognition similar across the 3 diagnostic groups. No significant linkage evidence to PCH1–PCH3 or individual neurocognitive measures was discovered. Conclusions: PCH1 is highly heritable and genetically correlated with SZ. It should prove useful in future genetic analyses. Mean PCH2 differentiates SZ families and controls but not SZ and unaffected family members. Oxford University Press 2013-03 2012-01-10 /pmc/articles/PMC3576168/ /pubmed/22234486 http://dx.doi.org/10.1093/schbul/sbr161 Text en © The Authors 2012. Published by Oxford University Press on behalf of the Maryland Psychiatric Research Center. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Regular Article Wiener, Howard Klei, Lambertus Calkins, Monica Wood, Joel Nimgaonkar, Vishwajit Gur, Ruben Bradford, L. DiAnne Richard, Jan Edwards, Neil Savage, Robert Kwentus, Joseph Allen, Trina McEvoy, Joseph Santos, Alberto Gur, Raquel Devlin, Bernie Go, Rodney Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects |
title | Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects |
title_full | Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects |
title_fullStr | Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects |
title_full_unstemmed | Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects |
title_short | Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects |
title_sort | principal components of heritability from neurocognitive domains differ between families with schizophrenia and control subjects |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3576168/ https://www.ncbi.nlm.nih.gov/pubmed/22234486 http://dx.doi.org/10.1093/schbul/sbr161 |
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