Multivariate analysis reveals shared genetic architecture of brain morphology and human behavior

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作者
Ronald de Vlaming
Eric A. W. Slob
Philip R. Jansen
Alain Dagher
Philipp D. Koellinger
Patrick J. F. Groenen
Cornelius A. Rietveld
机构
[1] Vrije Universiteit Amsterdam,School of Business and Economics
[2] Department of Applied Economics,MRC Biostatistics Unit, School of Clinical Medicine
[3] Erasmus School of Economics,Montreal Neurological Institute
[4] Erasmus University Rotterdam Institute for Behavior and Biology,La Follette School of Public Affairs
[5] Erasmus School of Economics,undefined
[6] University of Cambridge,undefined
[7] Department of Complex Trait Genetics,undefined
[8] Center for Neurogenomics and Cognitive Research,undefined
[9] Amsterdam Neuroscience,undefined
[10] Vrije Universiteit Amsterdam,undefined
[11] Department of Clinical Genetics,undefined
[12] VU Medical Center,undefined
[13] Amsterdam UMC,undefined
[14] McGill University,undefined
[15] University of Wisconsin-Madison,undefined
[16] Econometric Institute,undefined
[17] Erasmus School of Economics,undefined
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摘要
Human variation in brain morphology and behavior are related and highly heritable. Yet, it is largely unknown to what extent specific features of brain morphology and behavior are genetically related. Here, we introduce a computationally efficient approach for multivariate genomic-relatedness-based restricted maximum likelihood (MGREML) to estimate the genetic correlation between a large number of phenotypes simultaneously. Using individual-level data (N = 20,190) from the UK Biobank, we provide estimates of the heritability of gray-matter volume in 74 regions of interest (ROIs) in the brain and we map genetic correlations between these ROIs and health-relevant behavioral outcomes, including intelligence. We find four genetically distinct clusters in the brain that are aligned with standard anatomical subdivision in neuroscience. Behavioral traits have distinct genetic correlations with brain morphology which suggests trait-specific relevance of ROIs. These empirical results illustrate how MGREML can be used to estimate internally consistent and high-dimensional genetic correlation matrices in large datasets.
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