Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions
Clara A. MoreauiD, Kuldeep KumariD, Annabelle HarveyiD, Guillaume HuguetiD, Sebastian Georg Wenzel UrchsiD, Elise A. DouardiD, Laura M. SchultziD, Hanad Sharmarke, Khadijé JiziiD, Charles-Olivier MartiniD, Nadine Younis, Petra TameriD, Thomas RollandiD, Martineau Jean‐LouisiD, Pierre OrbaniD, David ShiniD, Ana Isabel SilvaiD, Jérémy HalliD, Marianne B. M. van den BreeiD, Michael John OweniD, David E.J. LindeniD, Aurélie LabbeiD, Anne Manuela MaillardiD, Tomasz Jan NowakowskiiD, Sarah LippéiD, , Sébastien JacquemontiD
Abstract
Polygenicity and pleiotropy are key properties of the genomic architecture of psychiatric disorders. An optimistic interpretation of polygenicity is that genomic variants converge on a limited set of mechanisms at some level from genes to behavior. Alternatively, convergence may be minimal or absent. We took advantage of brain connectivity, measured by resting-state functional MRI (rs- fMRI), as well as rare and common genomic variants to understand the effects of polygenicity and pleiotropy on large-scale brain networks, a distal step from genes to behavior. We processed ten rs-fMRI datasets including 32,988 individuals, to examine connectome-wide effects of 16 copy number variants (CNVs), 10 polygenic scores, 6 cognitive and brain morphometry traits, and 4 idiopathic psychiatric conditions. Although effect sizes of CNVs on connectivity were correlated to cognition and number of genes, increasing polygenicity was associated with decreasing effect sizes on connectivity. Accordingly, the effect sizes of polygenic scores on connectivity were 6-fold lower compared to CNVs. Despite this heterogeneity of connectivity profiles, multivariate analysis identified convergence of genetic risks and psychiatric disorders on the thalamus and the somatomotor network. Based on spatial correlations with transcriptomic data, we hypothesize that excitatory thalamic neurons may be primary contributors to brain alteration profiles shared across genetic risks and conditions. Finally, pleiotropy measured by genetic and transcriptomic correlations between 38 pairs of conditions/traits showed significant concordance with connectomic correlations, suggesting a substantial causal genetic component for shared connectivity. Such findings open avenues to delineate general mechanisms - amenable to intervention - across conditions and genetic risks. One sentence summaryEffects of rare and common genomic variants on brain functional connectivity shed light on the impact of polygenicity and pleiotropy in psychiatry.
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