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Improving genetic prediction by leveraging genetic correlations among human diseases and traits

Title: Improving genetic prediction by leveraging genetic correlations among human diseases and traits
Authors: Maier,Robert M.; Zhu,Zhihong; Lee,Sang Hong; Trzaskowski,Maciej; Ruderfer,Douglas M.; Stahl,Eli A.; Ripke,Stephan; Wray,Naomi R.; Yang,Jian; Visscher,Peter M.; Robinson,Matthew R.; Forstner,Andreas J.; Mcquillin,Andrew; Trubetskoy,Vassily; Wang,Weiqing; Wang,Yunpeng; Coleman,Jonathan R.I.; Gaspar,Héléna A.; De Leeuw,Christiaan A.; Whitehead Pavlides,Jennifer M.; Olde Loohuis,Loes M.; Pers,Tune H.; Lee,Phil H.; Charney,Alexander W.; Dobbyn,Amanda L.; Huckins,Laura; Boocock,James; Giambartolomei,Claudia; Roussos,Panos; Mullins,Niamh; Awasthi,Swapnil; Agerbo,Esben; Als,Thomas D.; Pedersen,Carsten Bøcker; Grove,Jakob; Kupka,Ralph; Regeer,Eline J.; Anjorin,Adebayo; Casas,Miquel; Mahon,Pamela B.; Allardyce,Judith; Escott-Price,Valentina; Forty,Liz; Fraser,Christine; Kogevinas,Manolis; Frank,Josef; Streit,Fabian; Strohmaier,Jana; Treutlein,Jens; Witt,Stephanie H.; Kennedy,James L.; Strauss,John S.; Garnham,Julie; O'donovan,Claire; Slaney,Claire; Steinberg,Stacy; Thorgeirsson,Thorgeir E.; Hautzinger,Martin; Steffens,Michael; Perlis,Roy H.; Sánchez-Mora,Cristina; Hipolito,Maria; Lawson,William B.; Nwulia,Evaristus A.; Levy,Shawn E.; Foroud,Tatiana M.; Jamain,Stéphane; Young,Allan H.; Mckay,James D.; Albani,Diego; Zandi,Peter; Potash,James B.; Zhang,Peng; Raymond Depaulo,J.; Bergen,Sarah E.; Juréus,Anders; Karlsson,Robert; Kandaswamy,Radhika; Mcguffin,Peter; Rivera,Margarita; Lissowska,Jolanta; Cruceanu,Cristiana; Lucae,Susanne; Cervantes,Pablo; Budde,Monika; Gade,Katrin; Heilbronner,Urs; Pedersen,Marianne Giørtz; Morris,Derek W.; Weickert,Cynthia Shannon; Weickert,Thomas W.; Macintyre,Donald J.; Lawrence,Jacob; Elvsåshagen,Torbjørn; Smeland,Olav B.; Djurovic,Srdjan; Xi,Simon; Green,Elaine K.; Czerski,Piotr M.; Hauser,Joanna; Xu,Wei; Vedder,Helmut; Oruc,Lilijana; Spijker,Anne T.; Gordon,Scott D.; Medland,Sarah E.; Curtis,David; Mühleisen,Thomas W.; Badner,Judith; Scheftner,William A.; Sigurdsson,Engilbert; Schork,Nicholas J.; Schatzberg,Alan F.; Bækvad-Hansen,Marie; Bybjerg-Grauholm,Jonas; Hansen,Christine Søholm; Knowles,James A.; Szelinger,Szabolcs; Montgomery,Grant W.; Boks, Marco; Adolfsson,Annelie Nordin; Hoffmann,Per; Bauer,Michael; Pfennig,Andrea; Leber,Markus; Kittel-Schneider,Sarah; Reif,Andreas; Del-Favero,Jurgen; Fischer,Sascha B.; Herms,Stefan; Reinbold,Céline S.; Degenhardt,Franziska; Koller,Anna C.; Maaser,Anna; Ori,Anil; Dale,Anders M.; Fan,Chun Chieh; Greenwood,Tiffany A.; Nievergelt,Caroline M.; Shehktman,Tatyana; Shilling,Paul D.; Byerley,William; Bunney,William; Alliey-Rodriguez,Ney; Clarke,Toni Kim; Liu,Chunyu; Coryell,William; Akil,Huda; Burmeister,Margit; Flickinger,Matthew; Li,Jun Z.; Mcinnis,Melvin G.; Meng,Fan; Thompson,Robert C.; Watson,Stanley J.; Zollner,Sebastian; Guan,Weihua; Green,Melissa J.; Craig,David; Sobell,Janet L.; Milani,Lili; Gordon-Smith,Katherine; Knott,Sarah V.; Perry,Amy; Parra,José Guzman; Mayoral,Fermin; Rivas,Fabio; Rice,John P.; Barchas,Jack D.; Børglum,Anders D.; Mortensen,Preben Bo; Mors,Ole; Grigoroiu-Serbanescu,Maria; Bellivier,Frank; Etain,Bruno; Leboyer,Marion; Ramos-Quiroga,Josep Antoni; Agartz,Ingrid; Amin,Farooq; Azevedo,Maria H.; Bass,Nicholas; Black,Donald W.; Blackwood,Douglas H.R.; Bruggeman,Richard; Buccola,Nancy G.; Choudhury,Khalid; Cloninger,C. Robert; Corvin,Aiden; Craddock,Nicholas; Daly,Mark J.; Datta,Susmita; Donohoe,Gary J.; Duan,Jubao; Dudbridge,Frank; Fanous,Ayman; Freedman,Robert; Freimer,Nelson B.; Friedl,Marion; Gill,Michael; Gurling,Hugh; De Haan,Lieuwe; Hamshere,Marian L.; Hartmann,Annette M.; Holmans,Peter A.; Kahn, René S.; Keller,Matthew C.; Kenny,Elaine; Kirov,George K.; Krabbendam,Lydia; Krasucki,Robert; Lencz,Todd; Levinson,Douglas F.; Lieberman,Jeffrey A.; Lin,Dan Yu; Linszen,Don H.; Magnusson,Patrik K.E.; Maier,Wolfgang; Malhotra,Anil K.; Mattheisen,Manuel; Mattingsdal,Morten; Mccarroll,Steven A.; Medeiros,Helena; Melle,Ingrid; Milanova,Vihra; Myin-Germeys,Inez; Neale,Benjamin M.; Ophoff, Roel A.; Owen,Michael J.; Pimm,Jonathan; Purcell,Shaun M.; Puri,Vinay; Quested,Digby J.; Rossin,Lizzy; Sanders,Alan R.; Shi,Jianxin; Sklar,Pamela; St Clair,David; Stroup,T. Scott; Van Os, Jim; Wiersma,Durk; Zammit,Stanley; Onderzoeksgroep 2; Brain; Onderzoeksgroep 11; Hersenen-Bedrijfsvoering
Publication Year: 2018
Subject Terms: General Chemistry; General Biochemistry,Genetics and Molecular Biology; General Physics and Astronomy
Description: Genomic prediction has the potential to contribute to precision medicine. However, to date, the utility of such predictors is limited due to low accuracy for most traits. Here theory and simulation study are used to demonstrate that widespread pleiotropy among phenotypes can be utilised to improve genomic risk prediction. We show how a genetic predictor can be created as a weighted index that combines published genome-wide association study (GWAS) summary statistics across many different traits. We apply this framework to predict risk of schizophrenia and bipolar disorder in the Psychiatric Genomics consortium data, finding substantial heterogeneity in prediction accuracy increases across cohorts. For six additional phenotypes in the UK Biobank data, we find increases in prediction accuracy ranging from 0.7% for height to 47% for type 2 diabetes, when using a multi-trait predictor that combines published summary statistics from multiple traits, as compared to a predictor based only on one trait.
Document Type: article in journal/newspaper
File Description: text/plain
Language: English
ISSN: 2041-1723
Relation: https://dspace.library.uu.nl/handle/1874/377086
Availability: https://dspace.library.uu.nl/handle/1874/377086
Rights: info:eu-repo/semantics/OpenAccess
Accession Number: edsbas.2A01974E
Database: BASE