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Genetic Diversity and Association Studies in US Hispanic/Latino Populations: Applications in the Hispanic Community Health Study/Study of Latinos.
Conomos, Matthew P; Laurie, Cecelia A; Stilp, Adrienne M; Gogarten, Stephanie M; McHugh, Caitlin P; Nelson, Sarah C; Sofer, Tamar; Fernández-Rhodes, Lindsay; Justice, Anne E; Graff, Mariaelisa; Young, Kristin L; Seyerle, Amanda A; Avery, Christy L; Taylor, Kent D; Rotter, Jerome I; Talavera, Gregory A; Daviglus, Martha L; Wassertheil-Smoller, Sylvia; Schneiderman, Neil; Heiss, Gerardo; Kaplan, Robert C; Franceschini, Nora; Reiner, Alex P; Shaffer, John R; Barr, R Graham; Kerr, Kathleen F; Browning, Sharon R; Browning, Brian L; Weir, Bruce S; Avilés-Santa, M Larissa; Papanicolaou, George J; Lumley, Thomas; Szpiro, Adam A; North, Kari E; Rice, Ken; Thornton, Timothy A; Laurie, Cathy C.
  • Conomos MP; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA. Electronic address: mconomos@uw.edu.
  • Laurie CA; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Stilp AM; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Gogarten SM; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • McHugh CP; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Nelson SC; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Sofer T; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Fernández-Rhodes L; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Justice AE; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Graff M; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Young KL; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Seyerle AA; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Avery CL; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Taylor KD; Institute for Translational Genomics and Population Sciences, Los Angeles Biomedical Research Institute and Department of Pediatrics, Harbor-UCLA Medical Center, Torrance, CA 90502, USA.
  • Rotter JI; Institute for Translational Genomics and Population Sciences, Los Angeles Biomedical Research Institute and Department of Pediatrics, Harbor-UCLA Medical Center, Torrance, CA 90502, USA.
  • Talavera GA; Graduate School of Public Health, San Diego State University, San Diego, CA 92182 USA.
  • Daviglus ML; Institute for Minority Health, University of Illinois at Chicago, Chicago, IL 60612, USA.
  • Wassertheil-Smoller S; Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
  • Schneiderman N; Department of Psychology and Behavioral Medicine, University of Miami, Miami, FL 33124, USA.
  • Heiss G; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Kaplan RC; Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
  • Franceschini N; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Reiner AP; Department of Epidemiology, University of Washington, Seattle, WA 98195, USA.
  • Shaffer JR; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA 15261, USA.
  • Barr RG; Departments of Medicine and Epidemiology, Columbia University Medical Center, New York, NY 10032, USA.
  • Kerr KF; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Browning SR; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Browning BL; Department of Medicine, University of Washington, Seattle, WA 98077, USA.
  • Weir BS; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Avilés-Santa ML; Division of Cardiovascular Sciences, NHLBI, NIH, Bethesda, MD 20892, USA.
  • Papanicolaou GJ; Division of Cardiovascular Sciences, NHLBI, NIH, Bethesda, MD 20892, USA.
  • Lumley T; Department of Statistics, University of Auckland, Auckland 1010, New Zealand.
  • Szpiro AA; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • North KE; Department of Epidemiology, University of North Carolina, Chapel Hill, NC 27514, USA.
  • Rice K; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Thornton TA; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA.
  • Laurie CC; Department of Biostatistics, University of Washington, Seattle, WA 98195, USA. Electronic address: cclaurie@uw.edu.
Am J Hum Genet ; 98(1): 165-84, 2016 Jan 07.
Article en En | MEDLINE | ID: mdl-26748518
ABSTRACT
US Hispanic/Latino individuals are diverse in genetic ancestry, culture, and environmental exposures. Here, we characterized and controlled for this diversity in genome-wide association studies (GWASs) for the Hispanic Community Health Study/Study of Latinos (HCHS/SOL). We simultaneously estimated population-structure principal components (PCs) robust to familial relatedness and pairwise kinship coefficients (KCs) robust to population structure, admixture, and Hardy-Weinberg departures. The PCs revealed substantial genetic differentiation within and among six self-identified background groups (Cuban, Dominican, Puerto Rican, Mexican, and Central and South American). To control for variation among groups, we developed a multi-dimensional clustering method to define a "genetic-analysis group" variable that retains many properties of self-identified background while achieving substantially greater genetic homogeneity within groups and including participants with non-specific self-identification. In GWASs of 22 biomedical traits, we used a linear mixed model (LMM) including pairwise empirical KCs to account for familial relatedness, PCs for ancestry, and genetic-analysis groups for additional group-associated effects. Including the genetic-analysis group as a covariate accounted for significant trait variation in 8 of 22 traits, even after we fit 20 PCs. Additionally, genetic-analysis groups had significant heterogeneity of residual variance for 20 of 22 traits, and modeling this heteroscedasticity within the LMM reduced genomic inflation for 19 traits. Furthermore, fitting an LMM that utilized a genetic-analysis group rather than a self-identified background group achieved higher power to detect previously reported associations. We expect that the methods applied here will be useful in other studies with multiple ethnic groups, admixture, and relatedness.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Hispánicos o Latinos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans País como asunto: America do norte Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Variación Genética / Hispánicos o Latinos Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Humans País como asunto: America do norte Idioma: En Año: 2016 Tipo del documento: Article