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Abstract

Genome-wide association studies (GWAS) have laid the foundation for investigations into the biology of complex traits, drug development and clinical guidelines. However, the majority of discovery efforts are based on data from populations of European ancestry. In light of the differential genetic architecture that is known to exist between populations, bias in representation can exacerbate existing disease and healthcare disparities. Critical variants may be missed if they have a low frequency or are completely absent in European populations, especially as the field shifts its attention towards rare variants, which are more likely to be population-specific. Additionally, effect sizes and their derived risk prediction scores derived in one population may not accurately extrapolate to other populations. Here we demonstrate the value of diverse, multi-ethnic participants in large-scale genomic studies. The Population Architecture using Genomics and Epidemiology (PAGE) study conducted a GWAS of 26 clinical and behavioural phenotypes in 49,839 non-European individuals. Using strategies tailored for analysis of multi-ethnic and admixed populations, we describe a framework for analysing diverse populations, identify 27 novel loci and 38 secondary signals at known loci, as well as replicate 1,444 GWAS catalogue associations across these traits. Our data show evidence of effect-size heterogeneity across ancestries for published GWAS associations, substantial benefits for fine-mapping using diverse cohorts and insights into clinical implications. In the United States-where minority populations have a disproportionately higher burden of chronic conditions-the lack of representation of diverse populations in genetic research will result in inequitable access to precision medicine for those with the highest burden of disease. We strongly advocate for continued, large genome-wide efforts in diverse populations to maximize genetic discovery and reduce health disparities.

Details

Title
Genetic analyses of diverse populations improves discovery for complex traits
Author
Wojcik, Genevieve L 1 ; Graff, Mariaelisa 2 ; Nishimura, Katherine K 3 ; Tao, Ran 4 ; Haessler, Jeffrey 3 ; Gignoux, Christopher R; Highland, Heather M; Patel, Yesha M; Sorokin, Elena P; Avery, Christy L; Belbin, Gillian M; Bien, Stephanie A; Cheng, Iona; Cullina, Sinead; Hodonsky, Chani J; Hu, Yao; Huckins, Laura M; Jeff, Janina; Justice, Anne E; Kocarnik, Jonathan M; Lim, Unhee; Lin, Bridget M; Lu, Yingchang; Nelson, Sarah C; Park, Sung-Shim L; Poisner, Hannah; Preuss, Michael H; Richard, Melissa A; Schurmann, Claudia; Setiawan, Veronica W; Sockell, Alexandra; Vahi, Karan; Verbanck, Marie; Vishnu, Abhishek; Walker, Ryan W; Young, Kristin L; Zubair, Niha; Acuña-Alonso, Victor; Ambite, Jose Luis; Barnes, Kathleen C; Boerwinkle, Eric; Bottinger, Erwin P; Bustamante, Carlos D; Caberto, Christian; Canizales-Quinteros, Samuel; Conomos, Matthew P; Deelman, Ewa; Do, Ron; Doheny, Kimberly; Fernández-Rhodes, Lindsay; Fornage, Myriam; Hailu, Benyam; Heiss, Gerardo; Henn, Brenna M; Hindorff, Lucia A; Jackson, Rebecca D; Laurie, Cecelia A; Laurie, Cathy C; Li, Yuqing; Lin, Dan-Yu; Moreno-Estrada, Andres; Nadkarni, Girish; Norman, Paul J; Pooler, Loreall C; Reiner, Alexander P; Romm, Jane; Sabatti, Chiara; Sandoval, Karla; Sheng, Xin; Stahl, Eli A; Stram, Daniel O; Thornton, Timothy A; Wassel, Christina L; Wilkens, Lynne R; Winkler, Cheryl A; Yoneyama, Sachi; Buyske, Steven; Haiman, Christopher A; Kooperberg, Charles; Marchand, Loic Le; Loos, Ruth J F; Matise, Tara C; North, Kari E; Peters, Ulrike; Kenny, Eimear E; Carlson, Christopher S

 Department of Biomedical Data Science, Stanford University, Stanford, CA, USA 
 Department of Epidemiology, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA 
 Division of Public Health Science, Fred Hutchinson Cancer Research Center, Seattle, WA, USA 
 Department of Biostatistics, Vanderbilt University Medical Center, Nashville, TN, USA 
Pages
514-2,518A-518G
Section
LETTER
Publication year
2019
Publication date
Jun 27, 2019
Publisher
Nature Publishing Group
ISSN
00280836
e-ISSN
14764687
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2251680280
Copyright
Copyright Nature Publishing Group Jun 27, 2019