TY - JOUR
T1 - Genomic relationships, novel loci, and pleiotropic mechanisms across eight psychiatric disorders
AU - Psychiat Genomics Consortium
AU - 23andMe Res Team
AU - Psychosis Endopheno-types Int Cons
AU - Wellcome Trust Case-Control Consor
AU - Lee, Phil H.
AU - Anttila, Verneri
AU - Won, Hyejung
AU - Feng, Yen-Chen A.
AU - Rosenthal, Jacob
AU - Zhu, Zhaozhong
AU - Tucker-Drob, Elliot M.
AU - Nivard, Michel G.
AU - Grotzinger, Andrew D.
AU - Posthuma, Danielle
AU - Wang, Meg M-J
AU - Yu, Dongmei
AU - Stahl, Eli A.
AU - Walters, Ray-mond K.
AU - Anney, Richard J. L.
AU - Duncan, Laramie E.
AU - Ge, Tian
AU - Adolfsson, Rolf
AU - Banaschewski, Tobias
AU - Belangero, Sintia
AU - Cook, Edwin H.
AU - Coppola, Giovanni
AU - Derks, Eske M.
AU - Hoekstra, Pieter J.
AU - Kaprio, Jaakko
AU - Keski-Rahkonen, Anna
AU - Kirov, George
AU - Kranzler, Henry R.
AU - Luykx, Jurjen J.
AU - Rohde, Luis A.
AU - Zai, Clement C.
AU - Agerbo, Esben
AU - Arranz, M. J.
AU - Asherson, Philip
AU - Baekvad-Hansen, Marie
AU - Baldursson, Gisli
AU - Bellgrove, Mark
AU - Belliveau, Richard A.
AU - Hartman, Catharina A.
AU - Jordan, Jennifer
AU - Kas, Martien J. H.
AU - Li, Dong
AU - Adams, Mark J.
AU - de Geus, E. J. C.
AU - Penninx, Brenda W. J. H.
AU - Cath, Danielle
AU - Dietrich, Andrea
AU - Kim, Young Key
AU - Kendler, Kenneth S.
PY - 2019/12/12
Y1 - 2019/12/12
N2 - Genetic influences on psychiatric disorders transcend diagnostic boundaries, suggesting substantial pleiotropy of contributing loci. However, the nature and mechanisms of these pleiotropic effects remain unclear. We performed analyses of 232,964 cases and 494,162 controls from genome-wide studies of anorexia nervosa, attention-deficit/hyper-activity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, and Tourette syndrome. Genetic correlation analyses revealed a meaningful structure within the eight disorders, identifying three groups of inter-related disorders. Meta-analysis across these eight disorders detected 109 loci associated with at least two psychiatric disorders, including 23 loci with pleiotropic effects on four or more disorders and 11 loci with antagonistic effects on multiple disorders. The pleiotropic loci are located within genes that show heightened expression in the brain throughout the lifespan, beginning prenatally in the second trimester, and play prominent roles in neurodevelopmental processes. These findings have important implications for psychiatric nosology, drug development, and risk prediction.
AB - Genetic influences on psychiatric disorders transcend diagnostic boundaries, suggesting substantial pleiotropy of contributing loci. However, the nature and mechanisms of these pleiotropic effects remain unclear. We performed analyses of 232,964 cases and 494,162 controls from genome-wide studies of anorexia nervosa, attention-deficit/hyper-activity disorder, autism spectrum disorder, bipolar disorder, major depression, obsessive-compulsive disorder, schizophrenia, and Tourette syndrome. Genetic correlation analyses revealed a meaningful structure within the eight disorders, identifying three groups of inter-related disorders. Meta-analysis across these eight disorders detected 109 loci associated with at least two psychiatric disorders, including 23 loci with pleiotropic effects on four or more disorders and 11 loci with antagonistic effects on multiple disorders. The pleiotropic loci are located within genes that show heightened expression in the brain throughout the lifespan, beginning prenatally in the second trimester, and play prominent roles in neurodevelopmental processes. These findings have important implications for psychiatric nosology, drug development, and risk prediction.
KW - WIDE ASSOCIATION
KW - HUMAN BRAIN
KW - GENETIC CORRELATIONS
KW - GENOTYPE IMPUTATION
KW - INSIGHTS
KW - IDENTIFICATION
KW - TRANSCRIPTOME
KW - DEMETHYLASE
KW - MUTATIONS
KW - DISEASES
U2 - 10.1016/j.cell.2019.11.020
DO - 10.1016/j.cell.2019.11.020
M3 - Article
SN - 0092-8674
VL - 179
SP - 1469-1482.e11
JO - Cell
JF - Cell
IS - 7
ER -