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Estimation of causal effects of a time-varying exposure at multiple time points through multivariable mendelian randomization.
Sanderson, Eleanor; Richardson, Tom G; Morris, Tim T; Tilling, Kate; Davey Smith, George.
Afiliação
  • Sanderson E; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, United Kingdom.
  • Richardson TG; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Morris TT; MRC Integrative Epidemiology Unit at the University of Bristol, Bristol, United Kingdom.
  • Tilling K; Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, United Kingdom.
  • Davey Smith G; Novo Nordisk Research Centre, Headington, Oxford, United Kingdom.
PLoS Genet ; 18(7): e1010290, 2022 07.
Article em En | MEDLINE | ID: mdl-35849575
ABSTRACT
Mendelian Randomisation (MR) is a powerful tool in epidemiology that can be used to estimate the causal effect of an exposure on an outcome in the presence of unobserved confounding, by utilising genetic variants as instrumental variables (IVs) for the exposure. The effect estimates obtained from MR studies are often interpreted as the lifetime effect of the exposure in question. However, the causal effects of some exposures are thought to vary throughout an individual's lifetime with periods during which an exposure has a greater effect on a particular outcome. Multivariable MR (MVMR) is an extension of MR that allows for multiple, potentially highly related, exposures to be included in an MR estimation. MVMR estimates the direct effect of each exposure on the outcome conditional on all the other exposures included in the estimation. We explore the use of MVMR to estimate the direct effect of a single exposure at different time points in an individual's lifetime on an outcome. We use simulations to illustrate the interpretation of the results from such analyses and the key assumptions required. We show that causal effects at different time periods can be estimated through MVMR when the association between the genetic variants used as instruments and the exposure measured at those time periods varies. However, this estimation will not necessarily identify exact time periods over which an exposure has the most effect on the outcome. Prior knowledge regarding the biological basis of exposure trajectories can help interpretation. We illustrate the method through estimation of the causal effects of childhood and adult BMI on C-Reactive protein and smoking behaviour.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Análise da Randomização Mendeliana Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Variação Genética / Análise da Randomização Mendeliana Tipo de estudo: Clinical_trials / Prognostic_studies Idioma: En Revista: PLoS Genet Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Reino Unido