학술논문

Genome-wide analysis in over 1 million individuals of European ancestry yields improved polygenic risk scores for blood pressure traits
Document Type
Article
Author
Keaton, Jacob M.Kamali, ZohaXie, TianVaez, AhmadWilliams, ArielGoleva, Slavina B.Ani, AlirezaEvangelou, EvangelosHellwege, Jacklyn N.Yengo, LoicYoung, William J.Traylor, MatthewGiri, AyushZheng, ZhiliZeng, JianChasman, Daniel I.Morris, Andrew P.Caulfield, Mark J.Hwang, Shih-JenKooner, Jaspal S.Conen, DavidAttia, John R.Morrison, Alanna C.Loos, Ruth J. F.Kristiansson, KatiSchmidt, ReinholdHicks, Andrew A.Pramstaller, Peter P.Nelson, Christopher P.Samani, Nilesh J.Risch, LorenzGyllensten, UlfMelander, OlleRiese, HarrietteWilson, James F.Campbell, HarryRich, Stephen S.Psaty, Bruce M.Lu, YingchangRotter, Jerome I.Guo, XiuqingRice, Kenneth M.Vollenweider, PeterSundström, JohanLangenberg, ClaudiaTobin, Martin D.Giedraitis, VilmantasLuan, Jian’anTuomilehto, JaakkoKutalik, ZoltanRipatti, SamuliSalomaa, VeikkoGirotto, GiorgiaTrompet, StellaJukema, J. Woutervan der Harst, PimRidker, Paul M.Giulianini, FrancoVitart, VeroniqueGoel, AnujWatkins, HughHarris, Sarah E.Deary, Ian J.van der Most, Peter J.Oldehinkel, Albertine J.Keavney, Bernard D.Hayward, CarolineCampbell, ArchieBoehnke, MichaelScott, Laura J.Boutin, ThibaudMamasoula, ChrysovalantoJärvelin, Marjo-RiittaPeters, AnnetteGieger, ChristianLakatta, Edward G.Cucca, FrancescoHui, JennieKnekt, PaulEnroth, StefanDe Borst, Martin H.Polašek, OzrenConcas, Maria PinaCatamo, EulaliaCocca, MassimilianoLi-Gao, RuifangHofer, EdithSchmidt, HelenaSpedicati, BeatriceWaldenberger, MelanieStrachan, David P.Laan, MarisTeumer, AlexanderDörr, MarcusGudnason, VilmundurCook, James P.Ruggiero, DanielaKolcic, IvanaBoerwinkle, EricTraglia, MichelaLehtimäki, TerhoRaitakari, Olli T.Johnson, Andrew D.Newton-Cheh, ChristopherBrown, Morris J.Dominiczak, Anna F.Sever, Peter J.Poulter, NeilChambers, John C.Elosua, RobertoSiscovick, DavidEsko, TõnuMetspalu, AndresStrawbridge, Rona J.Laakso, MarkkuHamsten, AndersHottenga, Jouke-Jande Geus, EcoMorris, Andrew D.Palmer, Colin N. A.Nolte, Ilja M.Milaneschi, YuriMarten, JonathanWright, AlanZeggini, EleftheriaHowson, Joanna M. M.O’Donnell, Christopher J.Spector, TimNalls, Mike A.Simonsick, Eleanor M.Liu, Yongmeivan Duijn, Cornelia M.Butterworth, Adam S.Danesh, John N.Menni, CristinaWareham, Nicholas J.Khaw, Kay-TeeSun, Yan V.Wilson, Peter W. F.Cho, KellyVisscher, Peter M.Denny, Joshua C.Levy, DanielEdwards, Todd L.Munroe, Patricia B.Snieder, HaroldWarren, Helen R.
Source
Nature Genetics; 20240101, Issue: Preprints p1-14, 14p
Subject
Language
ISSN
10614036; 15461718
Abstract
Hypertension affects more than one billion people worldwide. Here we identify 113 novel loci, reporting a total of 2,103 independent genetic signals (P< 5 × 10−8) from the largest single-stage blood pressure (BP) genome-wide association study to date (n= 1,028,980 European individuals). These associations explain more than 60% of single nucleotide polymorphism-based BP heritability. Comparing top versus bottom deciles of polygenic risk scores (PRSs) reveals clinically meaningful differences in BP (16.9 mmHg systolic BP, 95% CI, 15.5–18.2 mmHg, P= 2.22 × 10−126) and more than a sevenfold higher odds of hypertension risk (odds ratio, 7.33; 95% CI, 5.54–9.70; P= 4.13 × 10−44) in an independent dataset. Adding PRS into hypertension-prediction models increased the area under the receiver operating characteristic curve (AUROC) from 0.791 (95% CI, 0.781–0.801) to 0.826 (95% CI, 0.817–0.836, ∆AUROC, 0.035, P= 1.98 × 10−34). We compare the 2,103 loci results in non-European ancestries and show significant PRS associations in a large African-American sample. Secondary analyses implicate 500 genes previously unreported for BP. Our study highlights the role of increasingly large genomic studies for precision health research.