학술논문

Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.
Document Type
Author
Surendran, PraveenFeofanova, Elena VLahrouchi, NajimNtalla, IoannaKarthikeyan, SavitaCook, JamesChen, LingyanMifsud, BorbalaYao, ChenKraja, Aldi TCartwright, James HHellwege, Jacklyn NGiri, AyushTragante, ViniciusThorleifsson, GudmarLiu, Dajiang JPrins, Bram PStewart, Isobel DCabrera, Claudia PEales, James MAkbarov, ArturAuer, Paul LBielak, Lawrence FBis, Joshua CBraithwaite, Vickie SBrody, Jennifer ADaw, E WarwickWarren, Helen RDrenos, FotiosNielsen, Sune FallgaardFaul, Jessica DFauman, Eric BFava, CristianoFerreira, TeresaFoley, Christopher NFranceschini, NoraGao, HeGiannakopoulou, OlgaGiulianini, FrancoGudbjartsson, Daniel FGuo, XiuqingHarris, Sarah EHavulinna, Aki SHelgadottir, AnnaHuffman, Jennifer EHwang, Shih-JenKanoni, StavroulaKontto, JukkaLarson, Martin GLi-Gao, RuifangLindström, JaanaLotta, Luca ALu, YingchangLuan, Jian'anMahajan, AnubhaMalerba, GiovanniMasca, Nicholas G DMei, HaoMenni, CristinaMook-Kanamori, Dennis OMosen-Ansorena, DavidMüller-Nurasyid, MartinaParé, GuillaumePaul, Dirk SPerola, MarkusPoveda, AlaitzRauramaa, RainerRichard, MelissaRichardson, Tom GSepúlveda, NunoSim, XuelingSmith, Albert VSmith, Jennifer AStaley, James RStanáková, AlenaSulem, PatrickThériault, SébastienThorsteinsdottir, UnnurTrompet, StellaVarga, Tibor VVelez Edwards, Digna RVeronesi, GiovanniWeiss, StefanWillems, Sara MYao, JieYoung, RobinYu, BingZhang, WeihuaZhao, Jing-HuaZhao, WeiEvangelou, EvangelosAeschbacher, StefanieAsllanaj, EraldaBlankenberg, StefanBonnycastle, Lori LBork-Jensen, JetteBrandslund, IvanBraund, Peter SBurgess, StephenCho, KellyChristensen, CramerConnell, JohnMutsert, Renée deDominiczak, Anna FDörr, MarcusEiriksdottir, GudnyFarmaki, Aliki-EleniGaziano, J MichaelGrarup, NielsGrove, Megan LHallmans, GöranHansen, TorbenHave, Christian THeiss, GerardoJørgensen, Marit EJousilahti, PekkaKajantie, EeroKamat, MihirKäräjämäki, AnneMariKarpe, FredrikKoistinen, Heikki AKovesdy, Csaba PKuulasmaa, KariLaatikainen, TiinaLannfelt, LarsLee, I-TeLee, Wen-JaneLinneberg, AllanMartin, Lisa WMoitry, MarieNadkarni, GirishNeville, Matt JPalmer, Colin N APapanicolaou, George JPedersen, OlufPeters, JamesPoulter, NeilRasheed, AsifRasmussen, Katrine LRayner, N WilliamMägi, ReedikRenström, FridaRettig, RainerRossouw, JacquesSchreiner, Pamela JSever, Peter SSigurdsson, Emil LSkaaby, TeaSun, Yan VSundström, Johan, Professor, 1971; Thorgeirsson, GudmundurEsko, TõnuTrabetti, ElisabettaTsao, Philip STuomi, TiinamaijaTurner, Stephen TTzoulaki, IoannaVaartjes, IloncaVergnaud, Anne-ClaireWiller, Cristen JWilson, Peter W FWitte, Daniel RYonova-Doing, EkaterinaZhang, HeAliya, NaheedAlmgren, PeterAmouyel, PhilippeAsselbergs, Folkert WBarnes, Michael RBlakemore, Alexandra IBoehnke, MichaelBots, Michiel LBottinger, Erwin PBuring, Julie EChambers, John CChen, Yii-Der IdaChowdhury, RajivConen, DavidCorrea, AdolfoDavey Smith, GeorgeBoer, Rudolf A deDeary, Ian JDedoussis, GeorgeDeloukas, PanosDi Angelantonio, EmanueleElliott, PaulFelix, Stephan BFerrières, JeanFord, IanFornage, MyriamFranks, Paul WFranks, StephenFrossard, PhilippeGambaro, GiovanniGaunt, Tom RGroop, LeifGudnason, VilmundurHarris, Tamara BHayward, CarolineHennig, Branwen JHerzig, Karl-HeinzIngelsson, ErikTuomilehto, JaakkoJärvelin, Marjo-RiittaJukema, J WouterKardia, Sharon L RKee, FrankKooner, Jaspal SKooperberg, CharlesLauner, Lenore JLind, LarsLoos, Ruth J FMajumder, Abdulla Al ShafiLaakso, MarkkuMcCarthy, Mark IMelander, OlleMohlke, Karen LMurray, Alison DNordestgaard, Børge GrønneOrho-Melander, MarjuPackard, Chris JPadmanabhan, SandoshPalmas, WalterPolasek, OzrenPorteous, David JPrentice, Andrew MProvince, Michael ARelton, Caroline LRice, KennethRidker, Paul MRolandsson, OlovRosendaal, Frits RRotter, Jerome IRudan, IgorSalomaa, VeikkoSamani, Nilesh JSattar, NaveedSheu, Wayne H-HSmith, Blair HSoranzo, NicoleSpector, Timothy DStarr, John MSebert, SylvainTaylor, Kent DLakka, Timo ATimpson, Nicholas JTobin, Martin Dvan der Harst, Pimvan der Meer, PeterRamachandran, Vasan SVerweij, NiekVirtamo, JarmoVölker, UweWeir, David RZeggini, EleftheriaCharchar, Fadi JWareham, Nicholas JLangenberg, ClaudiaTomaszewski, MaciejButterworth, Adam SCaulfield, Mark JDanesh, JohnEdwards, Todd LHolm, HilmaHung, Adriana MLindgren, Cecilia MLiu, ChunyuManning, Alisa KMorris, Andrew PMorrison, Alanna CO'Donnell, Christopher JPsaty, Bruce MSaleheen, DanishStefansson, KariBoerwinkle, EricChasman, Daniel ILevy, DanielNewton-Cheh, ChristopherMunroe, Patricia BHowson, Joanna M M
Source
Nature Genetics. 52(12):1314-1332
Subject
Language
English
ISSN
1061-4036
1546-1718
Abstract
Genetic studies of blood pressure (BP) to date have mainly analyzed common variants (minor allele frequency > 0.05). In a meta-analysis of up to ~1.3 million participants, we discovered 106 new BP-associated genomic regions and 87 rare (minor allele frequency ≤ 0.01) variant BP associations (P < 5 × 10-8), of which 32 were in new BP-associated loci and 55 were independent BP-associated single-nucleotide variants within known BP-associated regions. Average effects of rare variants (44% coding) were ~8 times larger than common variant effects and indicate potential candidate causal genes at new and known loci (for example, GATA5 and PLCB3). BP-associated variants (including rare and common) were enriched in regions of active chromatin in fetal tissues, potentially linking fetal development with BP regulation in later life. Multivariable Mendelian randomization suggested possible inverse effects of elevated systolic and diastolic BP on large artery stroke. Our study demonstrates the utility of rare-variant analyses for identifying candidate genes and the results highlight potential therapeutic targets.