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Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies.
Sun, Quan; Graff, Misa; Rowland, Bryce; Wen, Jia; Huang, Le; Miller-Fleming, Tyne W; Haessler, Jeffrey; Preuss, Michael H; Chai, Jin-Fang; Lee, Moa P; Avery, Christy L; Cheng, Ching-Yu; Franceschini, Nora; Sim, Xueling; Cox, Nancy J; Kooperberg, Charles; North, Kari E; Li, Yun; Raffield, Laura M.
Afiliação
  • Sun Q; Department of Biostatistics, University of North Carolina, Chapel Hill, NC, USA.
  • Graff M; Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
  • Rowland B; Department of Biostatistics, University of North Carolina, Chapel Hill, NC, USA.
  • Wen J; Department of Genetics, University of North Carolina, Chapel Hill, NC, USA.
  • Huang L; Department of Genetics, University of North Carolina, Chapel Hill, NC, USA.
  • Miller-Fleming TW; Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Haessler J; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Preuss MH; The Charles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Chai JF; Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.
  • Lee MP; Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
  • Avery CL; Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
  • Cheng CY; Singapore Eye Research Institute, Singapore National Eye Centre, Singapore, Singapore.
  • Franceschini N; Ophthalmology & Visual Sciences Academic Clinical Program (Eye ACP), Duke-NUS Medical School, Singapore, Singapore.
  • Sim X; Department of Ophthalmology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
  • Cox NJ; Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
  • Kooperberg C; Saw Swee Hock School of Public Health, National University of Singapore and National University Health System, Singapore, Singapore.
  • North KE; Division of Genetic Medicine, Department of Medicine, Vanderbilt University Medical Center, Nashville, TN, USA.
  • Li Y; Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Raffield LM; Department of Epidemiology, University of North Carolina, Chapel Hill, NC, USA.
J Hum Genet ; 67(2): 87-93, 2022 Feb.
Article em En | MEDLINE | ID: mdl-34376796
ABSTRACT
Despite the dramatic underrepresentation of non-European populations in human genetics studies, researchers continue to exclude participants of non-European ancestry, as well as variants rare in European populations, even when these data are available. This practice perpetuates existing research disparities and can lead to important and large effect size associations being missed. Here, we conducted genome-wide association studies (GWAS) of 31 serum and urine biomarker quantitative traits in African (n = 9354), East Asian (n = 2559), and South Asian (n = 9823) ancestry UK Biobank (UKBB) participants. We adjusted for all known GWAS catalog variants for each trait, as well as novel signals identified in a recent European ancestry-focused analysis of UKBB participants. We identify 7 novel signals in African ancestry and 2 novel signals in South Asian ancestry participants (p < 1.61E-10). Many of these signals are highly plausible, including a cis pQTL for the gene encoding gamma-glutamyl transferase and PIEZO1 and G6PD variants with impacts on HbA1c through likely erythrocytic mechanisms. This work illustrates the importance of using the genetic data we already have in diverse populations, with novel discoveries possible in even modest sample sizes.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores / Bancos de Espécimes Biológicos / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Biomarcadores / Bancos de Espécimes Biológicos / Polimorfismo de Nucleotídeo Único / Locos de Características Quantitativas / Estudo de Associação Genômica Ampla Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País como assunto: Europa Idioma: En Ano de publicação: 2022 Tipo de documento: Article