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Mendelian randomization in the multivariate general linear model framework.
Allman, Phillip H; Aban, Inmaculada; Long, Dustin M; Patki, Amit; MacKenzie, Todd; Irvin, Marguerite R; Lange, Leslie A; Lange, Ethan; Cutter, Gary; Tiwari, Hemant K.
Afiliação
  • Allman PH; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Aban I; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Long DM; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Patki A; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • MacKenzie T; Department of Biomedical Data Science, Dartmouth College, Hanover, New Hampshire, USA.
  • Irvin MR; Department of Epidemiology, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Lange LA; Division of Biomedical Informatics and Personalized Medicine, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Lange E; Division of Biomedical Informatics and Personalized Medicine, Department of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
  • Cutter G; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
  • Tiwari HK; Department of Biostatistics, University of Alabama at Birmingham, Birmingham, Alabama, USA.
Genet Epidemiol ; 46(1): 17-31, 2022 02.
Article em En | MEDLINE | ID: mdl-34672390
ABSTRACT
Mendelian randomization (MR) is an application of instrumental variable (IV) methods to observational data in which the IV is a genetic variant. MR methods applicable to the general exponential family of distributions are currently not well characterized. We adapt a general linear model framework to the IV setting and propose a general MR method applicable to any full-rank distribution from the exponential family. Empirical bias and coverage are estimated via simulations. The proposed method is compared to several existing MR methods. Real data analyses are performed using data from the REGARDS study to estimate the potential causal effect of smoking frequency on stroke risk in African Americans. In simulations with binary variates and very weak instruments the proposed method had the lowest median [Q1 , Q3 ] bias (0.10 [-3.68 to 3.62]); compared with 2SPS (0.27 [-3.74 to 4.26]) and the Wald method (-0.69 [-1.72 to 0.35]). Low bias was observed throughout other simulation scenarios; as well as more than 90% coverage for the proposed method. In simulations with count variates, the proposed method performed comparably to 2SPS; the Wald method maintained the most consistent low bias; and 2SRI was biased towards the null. Real data analyses find no evidence for a causal effect of smoking frequency on stroke risk. The proposed MR method has low bias and acceptable coverage across a wide range of distributional scenarios and instrument strengths; and provides a more parsimonious framework for asymptotic hypothesis testing compared to existing two-stage procedures.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fumar / Análise da Randomização Mendeliana Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Genet Epidemiol Assunto da revista: EPIDEMIOLOGIA / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fumar / Análise da Randomização Mendeliana Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Humans Idioma: En Revista: Genet Epidemiol Assunto da revista: EPIDEMIOLOGIA / GENETICA MEDICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Estados Unidos