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Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes
INTRODUCTION: For many exposures present across the life course, the effect of the exposure may vary over time. Multivariable Mendelian randomization (MVMR) is an approach that can assess the effects of related risk factors using genetic variants as instrumental variables. Recently, MVMR has been us...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244034/ https://www.ncbi.nlm.nih.gov/pubmed/36661066 http://dx.doi.org/10.1093/ije/dyac240 |
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author | Tian, Haodong Burgess, Stephen |
author_facet | Tian, Haodong Burgess, Stephen |
author_sort | Tian, Haodong |
collection | PubMed |
description | INTRODUCTION: For many exposures present across the life course, the effect of the exposure may vary over time. Multivariable Mendelian randomization (MVMR) is an approach that can assess the effects of related risk factors using genetic variants as instrumental variables. Recently, MVMR has been used to estimate the effects of an exposure during distinct time periods. METHODS: We investigated the behaviour of estimates from MVMR in a simulation study for different time-varying causal scenarios. We also performed an applied analysis to consider how MVMR estimates of body mass index on systolic blood pressure vary depending on the time periods considered. RESULTS: Estimates from MVMR in the simulation study were close to the true values when the outcome model was correctly specified: i.e. when the outcome was a discrete function of the exposure at the precise time points at which the exposure was measured. However, in more realistic cases, MVMR estimates were misleading. For example, in one scenario, MVMR estimates for early life were clearly negative despite the true causal effect being constant and positive. In the applied example, estimates were highly variable depending on the time period in which genetic associations with the exposure were estimated. CONCLUSIONS: The poor performance of MVMR to study time-varying causal effects can be attributed to model misspecification and violation of the exclusion restriction assumption. We would urge caution about quantitative conclusions from such analyses and even qualitative interpretations about the direction, or presence or absence, of a causal effect during a given time period. |
format | Online Article Text |
id | pubmed-10244034 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-102440342023-06-08 Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes Tian, Haodong Burgess, Stephen Int J Epidemiol Methods INTRODUCTION: For many exposures present across the life course, the effect of the exposure may vary over time. Multivariable Mendelian randomization (MVMR) is an approach that can assess the effects of related risk factors using genetic variants as instrumental variables. Recently, MVMR has been used to estimate the effects of an exposure during distinct time periods. METHODS: We investigated the behaviour of estimates from MVMR in a simulation study for different time-varying causal scenarios. We also performed an applied analysis to consider how MVMR estimates of body mass index on systolic blood pressure vary depending on the time periods considered. RESULTS: Estimates from MVMR in the simulation study were close to the true values when the outcome model was correctly specified: i.e. when the outcome was a discrete function of the exposure at the precise time points at which the exposure was measured. However, in more realistic cases, MVMR estimates were misleading. For example, in one scenario, MVMR estimates for early life were clearly negative despite the true causal effect being constant and positive. In the applied example, estimates were highly variable depending on the time period in which genetic associations with the exposure were estimated. CONCLUSIONS: The poor performance of MVMR to study time-varying causal effects can be attributed to model misspecification and violation of the exclusion restriction assumption. We would urge caution about quantitative conclusions from such analyses and even qualitative interpretations about the direction, or presence or absence, of a causal effect during a given time period. Oxford University Press 2023-01-20 /pmc/articles/PMC10244034/ /pubmed/36661066 http://dx.doi.org/10.1093/ije/dyac240 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the International Epidemiological Association. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Tian, Haodong Burgess, Stephen Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes |
title | Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes |
title_full | Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes |
title_fullStr | Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes |
title_full_unstemmed | Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes |
title_short | Estimation of time-varying causal effects with multivariable Mendelian randomization: some cautionary notes |
title_sort | estimation of time-varying causal effects with multivariable mendelian randomization: some cautionary notes |
topic | Methods |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244034/ https://www.ncbi.nlm.nih.gov/pubmed/36661066 http://dx.doi.org/10.1093/ije/dyac240 |
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