학술논문

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
Document Type
Article
Author
Okbay, AysuBaselmans, Bart M LDe Neve, Jan-EmmanuelTurley, PatrickNivard, Michel GFontana, Mark AlanMeddens, S Fleur WLinnér, Richard KarlssonRietveld, Cornelius ADerringer, JaimeGratten, JacobLee, James JLiu, Jimmy Zde Vlaming, RonaldAhluwalia, Tarunveer SBuchwald, JadwigaCavadino, AlanaFrazier-Wood, Alexis CFurlotte, Nicholas AGarfield, VictoriaGeisel, Marie HenrikeGonzalez, Juan RHaitjema, SaskiaKarlsson, Robertvan der Laan, Sander WLadwig, Karl-HeinzLahti, Jarivan der Lee, Sven JLind, Penelope ALiu, TianMatteson, LindsayMihailov, EvelinMiller, Michael BMinica, Camelia CNolte, Ilja MMook-Kanamori, Dennisvan der Most, Peter JOldmeadow, ChristopherQian, YongRaitakari, OlliRawal, RajeshRealo, AnuRueedi, RicoSchmidt, BörgeSmith, Albert VStergiakouli, EvieTanaka, ToshikoTaylor, KentWedenoja, JuhoWellmann, JuergenWestra, Harm-JanWillems, Sara MZhao, WeiAmin, NajafBakshi, AndrewBoyle, Patricia ACherney, SamanthaCox, Simon RDavies, GailDavis, Oliver S PDing, JunDirek, NeseEibich, PeterEmeny, Rebecca TFatemifar, GhazalehFaul, Jessica DFerrucci, LuigiForstner, AndreasGieger, ChristianGupta, RichaHarris, Tamara BHarris, Juliette MHolliday, Elizabeth GHottenga, Jouke-JanDe Jager, Philip LKaakinen, Marika AKajantie, EeroKarhunen, VilleKolcic, IvanaKumari, MeenaLauner, Lenore JFranke, LudeLi-Gao, RuifangKoini, MarisaLoukola, AnuMarques-Vidal, PedroMontgomery, Grant WMosing, Miriam APaternoster, LaviniaPattie, AlisonPetrovic, Katja EPulkki-Råback, LauraQuaye, LydiaRäikkönen, KatriRudan, IgorScott, Rodney JSmith, Jennifer ASutin, Angelina RTrzaskowski, MaciejVinkhuyzen, Anna EYu, LeiZabaneh, DelilahAttia, John RBennett, David ABerger, KlausBertram, LarsBoomsma, Dorret ISnieder, HaroldChang, Shun-ChiaoCucca, FrancescoDeary, Ian Jvan Duijn, Cornelia MEriksson, Johan GBültmann, Utede Geus, Eco J CGroenen, Patrick J FGudnason, VilmundurHansen, TorbenHartman, Catharine AHaworth, Claire M AHayward, CarolineHeath, Andrew CHinds, David AHyppönen, ElinaIacono, William GJärvelin, Marjo-RiittaJöckel, Karl-HeinzKaprio, JaakkoKardia, Sharon L RKeltikangas-Järvinen, LiisaKraft, PeterKubzansky, Laura DLehtimäki, TerhoMagnusson, Patrik K EMartin, Nicholas GMcGue, MattMetspalu, AndresMills, Melindade Mutsert, RenéeOldehinkel, Albertine JPasterkamp, GerardPedersen, Nancy LPlomin, RobertPolasek, OzrenPower, ChristineRich, Stephen SRosendaal, Frits Rden Ruijter, Hester MSchlessinger, DavidSchmidt, HelenaSvento, RauliSchmidt, ReinholdAlizadeh, Behrooz ZSørensen, Thorkild I ASpector, Tim DSteptoe, AndrewTerracciano, AntonioThurik, A RoyTimpson, Nicholas JTiemeier, HenningUitterlinden, André GVollenweider, PeterWagner, Gert GWeir, David RYang, JianConley, Dalton CSmith, George DaveyHofman, AlbertJohannesson, MagnusLaibson, David IMedland, Sarah EMeyer, Michelle NPickrell, Joseph KEsko, TõnuKrueger, Robert FBeauchamp, Jonathan PKoellinger, Philipp DBenjamin, Daniel JBartels, MeikeCesarini, David
Source
Nature Genetics; May 2016, Vol. 48 Issue: 6 p624-633, 10p
Subject
Language
ISSN
10614036; 15461718
Abstract
Very few genetic variants have been associated with depression and neuroticism, likely because of limitations on sample size in previous studies. Subjective well-being, a phenotype that is genetically correlated with both of these traits, has not yet been studied with genome-wide data. We conducted genome-wide association studies of three phenotypes: subjective well-being (n = 298,420), depressive symptoms (n = 161,460), and neuroticism (n = 170,911). We identify 3 variants associated with subjective well-being, 2 variants associated with depressive symptoms, and 11 variants associated with neuroticism, including 2 inversion polymorphisms. The two loci associated with depressive symptoms replicate in an independent depression sample. Joint analyses that exploit the high genetic correlations between the phenotypes (|ρ^| ≈ 0.8) strengthen the overall credibility of the findings and allow us to identify additional variants. Across our phenotypes, loci regulating expression in central nervous system and adrenal or pancreas tissues are strongly enriched for association.