Rare copy number deletions predict individual variation in intelligence.

Phenotypic variation in human intellectual functioning shows substantial heritability, as demonstrated by a long history of behavior genetic studies. Many recent molecular genetic studies have attempted to uncover specific genetic variations responsible for this heritability, but identified effects...

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Main Authors: Ronald A Yeo, Steven W Gangestad, Jingyu Liu, Vince D Calhoun, Kent E Hutchison
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21298096/?tool=EBI
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spelling doaj-4bc5633323934590be236fe52dfa834a2021-03-03T19:54:00ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0161e1633910.1371/journal.pone.0016339Rare copy number deletions predict individual variation in intelligence.Ronald A YeoSteven W GangestadJingyu LiuVince D CalhounKent E HutchisonPhenotypic variation in human intellectual functioning shows substantial heritability, as demonstrated by a long history of behavior genetic studies. Many recent molecular genetic studies have attempted to uncover specific genetic variations responsible for this heritability, but identified effects capture little variance and have proven difficult to replicate. The present study, motivated an interest in "mutation load" emerging from evolutionary perspectives, examined the importance of the number of rare (or infrequent) copy number variations (CNVs), and the total number of base pairs included in such deletions, for psychometric intelligence. Genetic data was collected using the Illumina 1MDuoBeadChip Array from a sample of 202 adult individuals with alcohol dependence, and a subset of these (N = 77) had been administered the Wechsler Abbreviated Scale of Intelligence (WASI). After removing CNV outliers, the impact of rare genetic deletions on psychometric intelligence was investigated in 74 individuals. The total length of the rare deletions significantly and negatively predicted intelligence (r = -.30, p = .01). As prior studies have indicated greater heritability in individuals with relatively higher parental socioeconomic status (SES), we also examined the impact of ethnicity (Anglo/White vs. Other), as a proxy measure of SES; these groups did not differ on any genetic variable. This categorical variable significantly moderated the effect of length of deletions on intelligence, with larger effects being noted in the Anglo/White group. Overall, these results suggest that rare deletions (between 5% and 1% population frequency or less) adversely affect intellectual functioning, and that pleotropic effects might partly account for the association of intelligence with health and mental health status. Significant limitations of this research, including issues of generalizability and CNV measurement, are discussed.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21298096/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Ronald A Yeo
Steven W Gangestad
Jingyu Liu
Vince D Calhoun
Kent E Hutchison
spellingShingle Ronald A Yeo
Steven W Gangestad
Jingyu Liu
Vince D Calhoun
Kent E Hutchison
Rare copy number deletions predict individual variation in intelligence.
PLoS ONE
author_facet Ronald A Yeo
Steven W Gangestad
Jingyu Liu
Vince D Calhoun
Kent E Hutchison
author_sort Ronald A Yeo
title Rare copy number deletions predict individual variation in intelligence.
title_short Rare copy number deletions predict individual variation in intelligence.
title_full Rare copy number deletions predict individual variation in intelligence.
title_fullStr Rare copy number deletions predict individual variation in intelligence.
title_full_unstemmed Rare copy number deletions predict individual variation in intelligence.
title_sort rare copy number deletions predict individual variation in intelligence.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Phenotypic variation in human intellectual functioning shows substantial heritability, as demonstrated by a long history of behavior genetic studies. Many recent molecular genetic studies have attempted to uncover specific genetic variations responsible for this heritability, but identified effects capture little variance and have proven difficult to replicate. The present study, motivated an interest in "mutation load" emerging from evolutionary perspectives, examined the importance of the number of rare (or infrequent) copy number variations (CNVs), and the total number of base pairs included in such deletions, for psychometric intelligence. Genetic data was collected using the Illumina 1MDuoBeadChip Array from a sample of 202 adult individuals with alcohol dependence, and a subset of these (N = 77) had been administered the Wechsler Abbreviated Scale of Intelligence (WASI). After removing CNV outliers, the impact of rare genetic deletions on psychometric intelligence was investigated in 74 individuals. The total length of the rare deletions significantly and negatively predicted intelligence (r = -.30, p = .01). As prior studies have indicated greater heritability in individuals with relatively higher parental socioeconomic status (SES), we also examined the impact of ethnicity (Anglo/White vs. Other), as a proxy measure of SES; these groups did not differ on any genetic variable. This categorical variable significantly moderated the effect of length of deletions on intelligence, with larger effects being noted in the Anglo/White group. Overall, these results suggest that rare deletions (between 5% and 1% population frequency or less) adversely affect intellectual functioning, and that pleotropic effects might partly account for the association of intelligence with health and mental health status. Significant limitations of this research, including issues of generalizability and CNV measurement, are discussed.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21298096/?tool=EBI
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