학술논문

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology
Document Type
Original Paper
Author
Mullins, NiamhForstner, Andreas J.O’Connell, Kevin S.Coombes, BrandonColeman, Jonathan R. I.Qiao, ZhenAls, Thomas D.Bigdeli, Tim B.Børte, SigridBryois, JulienCharney, Alexander W.Drange, Ole KristianGandal, Michael J.Hagenaars, Saskia P.Ikeda, MasashiKamitaki, NolanKim, MinsooKrebs, KristiPanagiotaropoulou, GeorgiaSchilder, Brian M.Sloofman, Laura G.Steinberg, StacyTrubetskoy, VassilyWinsvold, Bendik S.Won, Hong-HeeAbramova, LiliyaAdorjan, KristinaAgerbo, EsbenAl Eissa, MariamAlbani, DiegoAlliey-Rodriguez, NeyAnjorin, AdebayoAntilla, VerneriAntoniou, AnastasiaAwasthi, SwapnilBaek, Ji HyunBækvad-Hansen, MarieBass, NicholasBauer, MichaelBeins, Eva C.Bergen, Sarah E.Birner, ArminBøcker Pedersen, CarstenBøen, ErlendBoks, Marco P.Bosch, RosaBrum, MurielleBrumpton, Ben M.Brunkhorst-Kanaan, NathalieBudde, MonikaBybjerg-Grauholm, JonasByerley, WilliamCairns, MurrayCasas, MiquelCervantes, PabloClarke, Toni-KimCruceanu, CristianaCuellar-Barboza, AlfredoCunningham, JulieCurtis, DavidCzerski, Piotr M.Dale, Anders M.Dalkner, NinaDavid, Friederike S.Degenhardt, FranziskaDjurovic, SrdjanDobbyn, Amanda L.Douzenis, AthanassiosElvsåshagen, TorbjørnEscott-Price, ValentinaFerrier, I. NicolFiorentino, AlessiaForoud, Tatiana M.Forty, LizFrank, JosefFrei, OleksandrFreimer, Nelson B.Frisén, LouiseGade, KatrinGarnham, JulieGelernter, JoelGiørtz Pedersen, MarianneGizer, Ian R.Gordon, Scott D.Gordon-Smith, KatherineGreenwood, Tiffany A.Grove, JakobGuzman-Parra, JoséHa, KyooseobHaraldsson, MagnusHautzinger, MartinHeilbronner, UrsHellgren, DennisHerms, StefanHoffmann, PerHolmans, Peter A.Huckins, LauraJamain, StéphaneJohnson, Jessica S.Kalman, Janos L.Kamatani, YoichiroKennedy, James L.Kittel-Schneider, SarahKnowles, James A.Kogevinas, ManolisKoromina, MariaKranz, Thorsten M.Kranzler, Henry R.Kubo, MichiakiKupka, RalphKushner, Steven A.Lavebratt, CatharinaLawrence, JacobLeber, MarkusLee, Heon-JeongLee, Phil H.Levy, Shawn E.Lewis, CatrinLiao, CalwingLucae, SusanneLundberg, MartinMacIntyre, Donald J.Magnusson, Sigurdur H.Maier, WolfgangMaihofer, AdamMalaspina, DoloresMaratou, EiriniMartinsson, LinaMattheisen, ManuelMcCarroll, Steven A.McGregor, Nathaniel W.McGuffin, PeterMcKay, James D.Medeiros, HelenaMedland, Sarah E.Millischer, VincentMontgomery, Grant W.Moran, Jennifer L.Morris, Derek W.Mühleisen, Thomas W.O’Brien, NiamhO’Donovan, ClaireOlde Loohuis, Loes M.Oruc, LilijanaPapiol, SergiPardiñas, Antonio F.Perry, AmyPfennig, AndreaPorichi, EvgeniaPotash, James B.Quested, DigbyRaj, TowfiqueRapaport, Mark H.DePaulo, J. RaymondRegeer, Eline J.Rice, John P.Rivas, FabioRivera, MargaritaRoth, JulianRoussos, PanosRuderfer, Douglas M.Sánchez-Mora, CristinaSchulte, Eva C.Senner, FannySharp, SallyShilling, Paul D.Sigurdsson, EngilbertSirignano, LeaSlaney, ClaireSmeland, Olav B.Smith, Daniel J.Sobell, Janet L.Søholm Hansen, ChristineSoler Artigas, MariaSpijker, Anne T.Stein, Dan J.Strauss, John S.Świątkowska, BeataTerao, ChikashiThorgeirsson, Thorgeir E.Toma, ClaudioTooney, PaulTsermpini, Evangelia-EiriniVawter, Marquis P.Vedder, HelmutWalters, James T. R.Witt, Stephanie H.Xi, SimonXu, WeiYang, Jessica Mei KayYoung, Allan H.Young, HannahZandi, Peter P.Zhou, HangZillich, LeaAdolfsson, RolfAgartz, IngridAlda, MartinAlfredsson, LarsBabadjanova, GuljaBacklund, LenaBaune, Bernhard T.Bellivier, FrankBengesser, SusanneBerrettini, Wade H.Blackwood, Douglas H. R.Boehnke, MichaelBørglum, Anders D.Breen, GeromeCarr, Vaughan J.Catts, StanleyCorvin, AidenCraddock, NicholasDannlowski, UdoDikeos, DimitrisEsko, TõnuEtain, BrunoFerentinos, PanagiotisFrye, MarkFullerton, Janice M.Gawlik, MichaGershon, Elliot S.Goes, Fernando S.Green, Melissa J.Grigoroiu-Serbanescu, MariaHauser, JoannaHenskens, FransHillert, JanHong, Kyung SueHougaard, David M.Hultman, Christina M.Hveem, KristianIwata, NakaoJablensky, Assen V.Jones, IanJones, Lisa A.Kahn, René S.Kelsoe, John R.Kirov, GeorgeLandén, MikaelLeboyer, MarionLewis, Cathryn M.Li, Qingqin S.Lissowska, JolantaLochner, ChristineLoughland, CarmelMartin, Nicholas G.Mathews, Carol A.Mayoral, FerminMcElroy, Susan L.McIntosh, Andrew M.McMahon, Francis J.Melle, IngridMichie, PatriciaMilani, LiliMitchell, Philip B.Morken, GunnarMors, OleMortensen, Preben BoMowry, BryanMüller-Myhsok, BertramMyers, Richard M.Neale, Benjamin M.Nievergelt, Caroline M.Nordentoft, MereteNöthen, Markus M.O’Donovan, Michael C.Oedegaard, Ketil J.Olsson, TomasOwen, Michael J.Paciga, Sara A.Pantelis, ChrisPato, CarlosPato, Michele T.Patrinos, George P.Perlis, Roy H.Posthuma, DanielleRamos-Quiroga, Josep AntoniReif, AndreasReininghaus, Eva Z.Ribasés, MartaRietschel, MarcellaRipke, StephanRouleau, Guy A.Saito, TakeoSchall, UlrichSchalling, MartinSchofield, Peter R.Schulze, Thomas G.Scott, Laura J.Scott, Rodney J.Serretti, AlessandroShannon Weickert, CynthiaSmoller, Jordan W.Stefansson, HreinnStefansson, KariStordal, EysteinStreit, FabianSullivan, Patrick F.Turecki, GustavoVaaler, Arne E.Vieta, EduardVincent, John B.Waldman, Irwin D.Weickert, Thomas W.Werge, ThomasWray, Naomi R.Zwart, John-AnkerBiernacka, Joanna M.Nurnberger, John I.Cichon, SvenEdenberg, Howard J.Stahl, Eli A.McQuillin, AndrewDi Florio, AriannaOphoff, Roel A.Andreassen, Ole A.
Source
Nature Genetics. 53(6):817-829
Subject
Language
English
ISSN
1061-4036
1546-1718
Abstract
Bipolar disorder is a heritable mental illness with complex etiology. We performed a genome-wide association study of 41,917 bipolar disorder cases and 371,549 controls of European ancestry, which identified 64 associated genomic loci. Bipolar disorder risk alleles were enriched in genes in synaptic signaling pathways and brain-expressed genes, particularly those with high specificity of expression in neurons of the prefrontal cortex and hippocampus. Significant signal enrichment was found in genes encoding targets of antipsychotics, calcium channel blockers, antiepileptics and anesthetics. Integrating expression quantitative trait locus data implicated 15 genes robustly linked to bipolar disorder via gene expression, encoding druggable targets such as HTR6, MCHR1, DCLK3 and FURIN. Analyses of bipolar disorder subtypes indicated high but imperfect genetic correlation between bipolar disorder type I and II and identified additional associated loci. Together, these results advance our understanding of the biological etiology of bipolar disorder, identify novel therapeutic leads and prioritize genes for functional follow-up studies.
Genome-wide association analyses of 41,917 bipolar disorder cases and 371,549 controls of European ancestry provide new insights into the etiology of this disorder and identify novel therapeutic leads and potential opportunities for drug repurposing.