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Extended methods for gene-environment-wide interaction scans in studies of admixed individuals with varying degrees of relationships.
Chen, Yalei; Adrianto, Indra; Ianuzzi, Michael C; Garman, Lori; Montgomery, Courtney G; Rybicki, Benjamin A; Levin, Albert M; Li, Jia.
Afiliação
  • Chen Y; Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan.
  • Adrianto I; Center for Bioinformatics, Henry Ford Health System, Detroit, Michigan.
  • Ianuzzi MC; Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan.
  • Garman L; Center for Bioinformatics, Henry Ford Health System, Detroit, Michigan.
  • Montgomery CG; Department of Internal Medicine, Northwell Staten Island University Hospital, Staten Island, New York, New York.
  • Rybicki BA; Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
  • Levin AM; Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, Oklahoma.
  • Li J; Department of Public Health Sciences, Henry Ford Health System, Detroit, Michigan.
Genet Epidemiol ; 43(4): 414-426, 2019 06.
Article em En | MEDLINE | ID: mdl-30793815
ABSTRACT
The etiology of many complex diseases involves both environmental exposures and inherited genetic predisposition as well as interactions between them. Gene-environment-wide interaction studies (GEWIS) provide a means to identify the interactions between genetic variation and environmental exposures that underlie disease risk. However, current GEWIS methods lack the capability to adjust for the potentially complex correlations in studies with varying degrees of relationships (both known and unknown) among individuals in admixed populations. We developed novel generalized estimating equation (GEE) based methods-GEE-adaptive and GEE-joint-to account for phenotypic correlations due to kinship while accounting for covariates, including, measures of genome-wide ancestry. In simulation studies of admixed individuals, both methods controlled family-wise error rates, an advantage over the case-only approach. They demonstrated higher power than traditional case-control methods across a wide range of underlying alternative hypotheses, especially where both marginal and interaction effects were present. We applied the proposed method to conduct a GEWIS of a known sarcoidosis risk factor (insecticide exposure) and risk of sarcoidosis in African Americans and identified two novel loci with suggestive evidence of G × E interaction.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoidose / Família / Estudo de Associação Genômica Ampla / Interação Gene-Ambiente Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sarcoidose / Família / Estudo de Associação Genômica Ampla / Interação Gene-Ambiente Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2019 Tipo de documento: Article