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Testing for risk and protective trends in genetic analyses of HIV acquisition.
Mccarthy, Janice M; Shea, Patrick R; Goldstein, David B; Allen, Andrew S.
Afiliação
  • Mccarthy JM; Department of Biostatistics and Bioinformatics, Duke University, Durham, NC 27710, USA.
  • Shea PR; Center for Human Genome Variation, Duke University, Durham, NC 27710, USA.
  • Goldstein DB; Center for Human Genome Variation, Duke University, Durham, NC 27710, USA.
  • Allen AS; Department of Biostatistics and Bioinformatics and Center for Human Genome Variation, Duke University, Durham, NC 27710, USA andrew.s.allen@duke.edu.
Biostatistics ; 16(2): 268-80, 2015 Apr.
Article em En | MEDLINE | ID: mdl-25270736
ABSTRACT
Host genetics studies of HIV-1 acquisition are critically important for the identification of new targets for drug and vaccine development. Analyses of such studies typically focus on pairwise comparisons of three different groups HIV-1 positive individuals, HIV-1 high-risk seronegative individuals, and population controls. Because there is a clear expectation of how gene frequencies of risk or protective alleles would be ordered in the three groups, we are able to construct a statistical framework that offers a consistent increase in power over a wide-range of the magnitude of risk/protective effects. In this paper, we develop tests that constrain the alternative hypothesis to appropriately reflect risk or protective trends jointly across the three groups and show that they lead to a substantial increase in power over the naive pairwise approach. We develop both likelihood-ratio and score statistics that test for genetic effects across the three groups while constraining the alternative hypothesis to reflect biologically motivated trends of risk or protection. The asymptotic distribution of both statistics (likelihood ratio and score) is derived. We investigate the performance of our approach via extensive simulation studies using a biologically motivated model of HIV-1 acquisition, and find that our proposed approach leads to an increase in power of roughly 10-28%. We illustrate our approach with an analysis of the effect of the CCR5Δ32 mutation on HIV acquisition.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Interpretação Estatística de Dados / Predisposição Genética para Doença / Modelos Teóricos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Infecções por HIV / Interpretação Estatística de Dados / Predisposição Genética para Doença / Modelos Teóricos Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article