作者
Luis M. García‐Marín,Adrián I. Campos,Santiago Diaz‐Torres,Jill A. Rabinowitz,Zuriel Ceja,Brittany L. Mitchell,Katrina L. Grasby,Jackson G. Thorp,Ingrid Agartz,Saud Alhusaini,David Ames,Philippe Amouyel,Ole A. Andreassen,Konstantinos Arfanakis,Alejandro Arias Vásquez,Nicola J. Armstrong,Lavinia Athanasiu,Mark E. Bastin,Alexa Beiser,David A. Bennett,Joshua C. Bis,Marco P. Boks,Dorret I. Boomsma,Henry Brodaty,Rachel M. Brouwer,Jan K. Buitelaar,Ralph Burkhardt,Wiepke Cahn,Vince D. Calhoun,Owen Carmichael,M. Mallar Chakravarty,Qiang Chen,Christopher R. K. Ching,Sven Cichon,Benedicto Crespo‐Facorro,Fabrice Crivello,Anders M. Dale,George Davey Smith,Eco J. C. de Geus,Philip L. De Jager,Greig I. de Zubicaray,Stéphanie Debette,Charles DeCarli,Chantal Depondt,Sylvane Desrivières,Srdjan Djurovic,Stefan Ehrlich,Susanne Erk,Thomas Espeseth,Guillén Fernández,Irina Filippi,Simon E. Fisher,Debra Fleischman,Evan Fletcher,Myriam Fornage,Andreas J. Forstner,Clyde Francks,Barbara Franke,Tian Ge,Aaron L. Goldman,Hans J. Grabe,Robert C. Green,O. Grimm,Nynke A. Groenewold,Oliver Gruber,Vilmundur Guðnason,Asta K. Håberg,Unn K. Haukvik,Andreas Heinz,Derrek P. Hibar,Saima Hilal,Jayandra J. Himali,Beng‐Choon Ho,David Hoehn,Pieter J. Hoekstra,Edith Hofer,Wolfgang Hoffmann,Avram J. Holmes,Georg Homuth,Norbert Hosten,M. Kamran Ikram,Jonathan Ipser,Clifford R. Jack,Neda Jahanshad,Erik G. Jönsson,René S. Kahn,Ryota Kanai,Marieke Klein,Maria J. Knol,Lenore J. Launer,Stephen M. Lawrie,Stéphanie Le Hellard,Phil H. Lee,Hervé Lemaître,Shuo Li,David C. Liewald,Honghuang Lin,W. T. Longstreth,Oscar L. López,Michelle Luciano
摘要
Abstract Subcortical brain structures are involved in developmental, psychiatric and neurological disorders. We performed GWAS meta-analyses of intracranial and nine subcortical brain volumes (brainstem, caudate nucleus, putamen, hippocampus, globus pallidus, thalamus, nucleus accumbens, amygdala and, for the first time, the ventral diencephalon) in 74,898 participants of European ancestry. We identified 254 independent loci associated with these brain volumes, explaining up to 35% of phenotypic variance. We observed gene expression in specific neural cell types across differentiation time points, including genes involved in intracellular signalling and brain ageing-related processes. Polygenic scores for brain volumes showed predictive ability when applied to individuals of diverse ancestries. We observed causal genetic effects of brain volumes with Parkinson’s disease and ADHD. Findings implicate specific gene expression patterns in brain development and genetic variants in comorbid neuropsychiatric disorders, which could point to a brain substrate and region of action for risk genes implicated in brain diseases.