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Atlas of functional connectivity relationships across rare and common genetic variants, traits, and psychiatric conditions

Authors :
Sarah Lippé
Carrie E. Bearden
Kuldeep Kumar
Elise Douard
Thomas Rolland
Jean-Louis Martineau
David Shin
Marianne Bernadette van den Bree
Hanad Sharmarke
Clara Moreau
Pierre Orban
Annabelle Harvey
Aurélie Labbe
Pierre Bellec
Laura M. Schultz
Guillaume Huguet
David Edmund Johannes Linden
Petra Tamer
Paul M. Thompson
Sebastian Urchs
Sébastien Jacquemont
Laura Almasy
Nadine Younis
David C. Glahn
Ana I. Silva
Anne M. Maillard
Tomasz J. Nowakowski
Thomas Bourgeron
Khadije Jizi
Charles-Olivier Martin
Michael John Owen
Jeremy Hall
Institut Pasteur [Paris] (IP)
Centre de recherche du CHU Sainte-Justine / Research Center of the Sainte-Justine University Hospital [Montreal, Canada]
Université de Montréal (UdeM)-CHU Sainte Justine [Montréal]
Génétique humaine et fonctions cognitives - Human Genetics and Cognitive Functions (GHFC (UMR_3571 / U-Pasteur_1))
Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité)
Université de Montréal (UdeM)
McGill University = Université McGill [Montréal, Canada]
Children’s Hospital of Philadelphia (CHOP )
Centre de Recherche de l'Institut Universitaire de Gériatrie de Montréal (CRIUGM)
Centre National de la Recherche Scientifique (CNRS)
University of California [San Francisco] (UC San Francisco)
University of California (UC)
Cardiff University
Maastricht University [Maastricht]
Centre Hospitalier Universitaire Vaudois [Lausanne] (CHUV)
University of California [Los Angeles] (UCLA)
University of Pennsylvania
Harvard Medical School [Boston] (HMS)
Boston Children's Hospital
Keck School of Medicine [Los Angeles]
University of Southern California (USC)
This research was supported by Compute Canada (ID 3037 and gsf-624), the Brain Canada Multi investigator research initiative (MIRI), Canada First Research Excellence Fund, Institute of Data Valorization, Healthy Brain Healthy Lives (Dr. Jacquemont). Dr. Jacquemont is a recipient of a Canada Research Chair in neurodevelopmental disorders, and a chair from the Jeanne et Jean Louis Levesque Foundation. This work was supported by a grant from the Brain Canada Multi-Investigator initiative (Dr. Jacquemont) and a grant from The Canadian Institutes of Health Research (CIHR 400528, Dr. Jacquemont). The Cardiff CNV cohort was supported by the Wellcome Trust Strategic Award 'DEFINE' and the National Centre for Mental Health with funds from Health and Care Research Wales (code 100202/Z/12/Z). The CHUV cohort was supported by the SNF (Maillard Anne, Project, PMPDP3 171331). Data from the UCLA cohort provided by Dr. Bearden (participants with 22q11.2 deletions or duplications and controls) was supported through grants from the NIH (U54EB020403), NIMH (R01MH085953, R01MH100900, 1U01MH119736, R21MH116473), and the Simons Foundation (SFARI Explorer Award). Finally, data from another study were obtained through the OpenFMRI project (http://openfmri.org) from the Consortium for Neuropsychiatric Phenomics (CNP), which was supported by NIH Roadmap for Medical Research grants UL1-DE019580, RL1MH083268, RL1MH083269, RL1DA024853, RL1MH083270, RL1LM009833, PL1MH083271, and PL1NS062410. Dr P. Bellec is a fellow ('Chercheur boursier Junior 2') of the 'Fonds de recherche du Québec - Santé', Data preprocessing and analyses were supported in part by the Courtois foundation (Dr Bellec). This work was supported by Simons Foundation Grant Nos. SFARI219193 and SFARI274424.
We thank all of the families at the participating Simons Variation in Individuals Project (VIP) sites, as well as the Simons VIP Consortium. We appreciate obtaining access to imaging and phenotypic data on SFARI Base. Approved researchers can obtain the Simons VIP population dataset described in this study by applying at https://base.sfari.org. We are grateful to all families who participated in the 16p11.2 European Consortium. Dr. P. Thompson was funded in part by the U.S. NIH grants R01MH116147, P41EB015922, R01MH111671, and U01 AG068057. Ms. Petra Tamer received the Canadian Institute of Health Research (CIHR) Scholarship.
Institut Pasteur [Paris]
Centre de recherche du CHU Sainte-Justine [Montreal]
Centre National de la Recherche Scientifique (CNRS)-Institut Pasteur [Paris]-Université de Paris (UP)
University of California [San Francisco] (UCSF)
University of California
University of Pennsylvania [Philadelphia]
Publication Year :
2021
Publisher :
HAL CCSD, 2021.

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.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....92cc250ef4e3cac0d4e5ee04c9c38474