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Constrained instruments and their application to Mendelian randomization with pleiotropy.
Jiang, Lai; Oualkacha, Karim; Didelez, Vanessa; Ciampi, Antonio; Rosa-Neto, Pedro; Benedet, Andrea L; Mathotaarachchi, Sulantha; Richards, John Brent; Greenwood, Celia M T.
Afiliação
  • Jiang L; Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada.
  • Oualkacha K; Department of Epidemiology, Biostatistics and Occupational Health and Gerald Bronfman Department of Oncology, McGill University, Montreal, Quebec, Canada.
  • Didelez V; Department of Mathematics, Université du Québec à Montréal, Montreal, Quebec, Canada.
  • Ciampi A; BIPS & Department of Mathematics, Leibinz Institute for Prevention Research and Epidemiology, University of Bremen, Bremen, Germany.
  • Rosa-Neto P; Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada.
  • Benedet AL; Department of Epidemiology, Biostatistics and Occupational Health and Gerald Bronfman Department of Oncology, McGill University, Montreal, Quebec, Canada.
  • Mathotaarachchi S; Department of Neurology & Neurosurgery, McGill University, Montreal, Quebec, Canada.
  • Richards JB; Translational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Douglas Hospital, McGill University, Montreal, Quebec, Canada.
  • Greenwood CMT; Translational Neuroimaging Laboratory, McGill University Research Centre for Studies in Aging, Douglas Hospital, McGill University, Montreal, Quebec, Canada.
Genet Epidemiol ; 43(4): 373-401, 2019 06.
Article em En | MEDLINE | ID: mdl-30635941
ABSTRACT
In Mendelian randomization (MR), inference about causal relationship between a phenotype of interest and a response or disease outcome can be obtained by constructing instrumental variables from genetic variants. However, MR inference requires three assumptions, one of which is that the genetic variants only influence the outcome through phenotype of interest. Pleiotropy, that is, the situation in which some genetic variants affect more than one phenotype, can invalidate these genetic variants for use as instrumental variables; thus a naive analysis will give biased estimates of the causal relation. Here, we present new methods (constrained instrumental variable [CIV] methods) to construct valid instrumental variables and perform adjusted causal effect estimation when pleiotropy exists and when the pleiotropic phenotypes are available. We demonstrate that a smoothed version of CIV performs approximate selection of genetic variants that are valid instruments, and provides unbiased estimates of the causal effects. We provide details on a number of existing methods, together with a comparison of their performance in a large series of simulations. CIV performs robustly across different pleiotropic violations of the MR assumptions. We also analyzed the data from the Alzheimer's disease (AD) neuroimaging initiative (ADNI; Mueller et al., 2005. Alzheimer's Dementia, 11(1), 55-66) to disentangle causal relationships of several biomarkers with AD progression.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise da Randomização Mendeliana / Pleiotropia Genética Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Genet Epidemiol Assunto da revista: EPIDEMIOLOGIA / GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Análise da Randomização Mendeliana / Pleiotropia Genética Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Genet Epidemiol Assunto da revista: EPIDEMIOLOGIA / GENETICA MEDICA Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Canadá