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Interpretation of Mendelian randomization using a single measure of an exposure that varies over time

BACKGROUND: Mendelian randomization (MR) is a powerful tool through which the causal effects of modifiable exposures on outcomes can be estimated from observational data. Most exposures vary throughout the life course, but MR is commonly applied to one measurement of an exposure (e.g. weight measure...

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Autores principales: Morris, Tim T, Heron, Jon, Sanderson, Eleanor C M, Davey Smith, George, Didelez, Vanessa, Tilling, Kate
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749705/
https://www.ncbi.nlm.nih.gov/pubmed/35848950
http://dx.doi.org/10.1093/ije/dyac136
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author Morris, Tim T
Heron, Jon
Sanderson, Eleanor C M
Davey Smith, George
Didelez, Vanessa
Tilling, Kate
author_facet Morris, Tim T
Heron, Jon
Sanderson, Eleanor C M
Davey Smith, George
Didelez, Vanessa
Tilling, Kate
author_sort Morris, Tim T
collection PubMed
description BACKGROUND: Mendelian randomization (MR) is a powerful tool through which the causal effects of modifiable exposures on outcomes can be estimated from observational data. Most exposures vary throughout the life course, but MR is commonly applied to one measurement of an exposure (e.g. weight measured once between ages 40 and 60 years). It has been argued that MR provides biased causal effect estimates when applied to one measure of an exposure that varies over time. METHODS: We propose an approach that emphasizes the liability that causes the entire exposure trajectory. We demonstrate this approach using simulations and an applied example. RESULTS: We show that rather than estimating the direct or total causal effect of changing the exposure value at a given time, MR estimates the causal effect of changing the underlying liability for the exposure, scaled to the effect of the liability on the exposure at that time. As such, results from MR conducted at different time points are expected to differ (unless the effect of the liability on exposure is constant over time), as we illustrate by estimating the effect of body mass index measured at different ages on systolic blood pressure. CONCLUSION: Univariable MR results should not be interpreted as time-point-specific direct or total causal effects, but as the effect of changing the liability for the exposure. Estimates of how the effects of a genetic variant on an exposure vary over time, together with biological knowledge that provides evidence regarding likely effective exposure periods, are required to interpret time-point-specific causal effects.
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spelling pubmed-97497052022-12-15 Interpretation of Mendelian randomization using a single measure of an exposure that varies over time Morris, Tim T Heron, Jon Sanderson, Eleanor C M Davey Smith, George Didelez, Vanessa Tilling, Kate Int J Epidemiol Methods BACKGROUND: Mendelian randomization (MR) is a powerful tool through which the causal effects of modifiable exposures on outcomes can be estimated from observational data. Most exposures vary throughout the life course, but MR is commonly applied to one measurement of an exposure (e.g. weight measured once between ages 40 and 60 years). It has been argued that MR provides biased causal effect estimates when applied to one measure of an exposure that varies over time. METHODS: We propose an approach that emphasizes the liability that causes the entire exposure trajectory. We demonstrate this approach using simulations and an applied example. RESULTS: We show that rather than estimating the direct or total causal effect of changing the exposure value at a given time, MR estimates the causal effect of changing the underlying liability for the exposure, scaled to the effect of the liability on the exposure at that time. As such, results from MR conducted at different time points are expected to differ (unless the effect of the liability on exposure is constant over time), as we illustrate by estimating the effect of body mass index measured at different ages on systolic blood pressure. CONCLUSION: Univariable MR results should not be interpreted as time-point-specific direct or total causal effects, but as the effect of changing the liability for the exposure. Estimates of how the effects of a genetic variant on an exposure vary over time, together with biological knowledge that provides evidence regarding likely effective exposure periods, are required to interpret time-point-specific causal effects. Oxford University Press 2022-07-15 /pmc/articles/PMC9749705/ /pubmed/35848950 http://dx.doi.org/10.1093/ije/dyac136 Text en © The Author(s) 2022. 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
Morris, Tim T
Heron, Jon
Sanderson, Eleanor C M
Davey Smith, George
Didelez, Vanessa
Tilling, Kate
Interpretation of Mendelian randomization using a single measure of an exposure that varies over time
title Interpretation of Mendelian randomization using a single measure of an exposure that varies over time
title_full Interpretation of Mendelian randomization using a single measure of an exposure that varies over time
title_fullStr Interpretation of Mendelian randomization using a single measure of an exposure that varies over time
title_full_unstemmed Interpretation of Mendelian randomization using a single measure of an exposure that varies over time
title_short Interpretation of Mendelian randomization using a single measure of an exposure that varies over time
title_sort interpretation of mendelian randomization using a single measure of an exposure that varies over time
topic Methods
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9749705/
https://www.ncbi.nlm.nih.gov/pubmed/35848950
http://dx.doi.org/10.1093/ije/dyac136
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