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Testing cross-phenotype effects of rare variants in longitudinal studies of complex traits.
Rudra, Pratyaydipta; Broadaway, K Alaine; Ware, Erin B; Jhun, Min A; Bielak, Lawrence F; Zhao, Wei; Smith, Jennifer A; Peyser, Patricia A; Kardia, Sharon L R; Epstein, Michael P; Ghosh, Debashis.
Afiliación
  • Rudra P; Department of Biostatistics and Informatics, Colorado School of Public Health, Aurora, Colorado, United States of America.
  • Broadaway KA; Department of Human Genetics, Emory University, Atlanta, Georgia, United States of America.
  • Ware EB; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Jhun MA; Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Bielak LF; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Zhao W; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Smith JA; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Peyser PA; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Kardia SLR; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Epstein MP; Department of Epidemiology, University of Michigan, Ann Arbor, Michigan, United States of America.
  • Ghosh D; Department of Human Genetics, Emory University, Atlanta, Georgia, United States of America.
Genet Epidemiol ; 42(4): 320-332, 2018 06.
Article en En | MEDLINE | ID: mdl-29601641
ABSTRACT
Many gene mapping studies of complex traits have identified genes or variants that influence multiple phenotypes. With the advent of next-generation sequencing technology, there has been substantial interest in identifying rare variants in genes that possess cross-phenotype effects. In the presence of such effects, modeling both the phenotypes and rare variants collectively using multivariate models can achieve higher statistical power compared to univariate methods that either model each phenotype separately or perform separate tests for each variant. Several studies collect phenotypic data over time and using such longitudinal data can further increase the power to detect genetic associations. Although rare-variant approaches exist for testing cross-phenotype effects at a single time point, there is no analogous method for performing such analyses using longitudinal outcomes. In order to fill this important gap, we propose an extension of Gene Association with Multiple Traits (GAMuT) test, a method for cross-phenotype analysis of rare variants using a framework based on the distance covariance. The approach allows for both binary and continuous phenotypes and can also adjust for covariates. Our simple adjustment to the GAMuT test allows it to handle longitudinal data and to gain power by exploiting temporal correlation. The approach is computationally efficient and applicable on a genome-wide scale due to the use of a closed-form test whose significance can be evaluated analytically. We use simulated data to demonstrate that our method has favorable power over competing approaches and also apply our approach to exome chip data from the Genetic Epidemiology Network of Arteriopathy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Carácter Cuantitativo Heredable Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genet Epidemiol Asunto de la revista: EPIDEMIOLOGIA / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Carácter Cuantitativo Heredable Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Genet Epidemiol Asunto de la revista: EPIDEMIOLOGIA / GENETICA MEDICA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos