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Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption

BACKGROUND: Two-sample summary-data Mendelian randomization (MR) incorporating multiple genetic variants within a meta-analysis framework is a popular technique for assessing causality in epidemiology. If all genetic variants satisfy the instrumental variable (IV) and necessary modelling assumptions...

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Autores principales: Bowden, Jack, Del Greco M, Fabiola, Minelli, Cosetta, Zhao, Qingyuan, Lawlor, Debbie A, Sheehan, Nuala A, Thompson, John, Davey Smith, George
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659376/
https://www.ncbi.nlm.nih.gov/pubmed/30561657
http://dx.doi.org/10.1093/ije/dyy258
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author Bowden, Jack
Del Greco M, Fabiola
Minelli, Cosetta
Zhao, Qingyuan
Lawlor, Debbie A
Sheehan, Nuala A
Thompson, John
Davey Smith, George
author_facet Bowden, Jack
Del Greco M, Fabiola
Minelli, Cosetta
Zhao, Qingyuan
Lawlor, Debbie A
Sheehan, Nuala A
Thompson, John
Davey Smith, George
author_sort Bowden, Jack
collection PubMed
description BACKGROUND: Two-sample summary-data Mendelian randomization (MR) incorporating multiple genetic variants within a meta-analysis framework is a popular technique for assessing causality in epidemiology. If all genetic variants satisfy the instrumental variable (IV) and necessary modelling assumptions, then their individual ratio estimates of causal effect should be homogeneous. Observed heterogeneity signals that one or more of these assumptions could have been violated. METHODS: Causal estimation and heterogeneity assessment in MR require an approximation for the variance, or equivalently the inverse-variance weight, of each ratio estimate. We show that the most popular ‘first-order’ weights can lead to an inflation in the chances of detecting heterogeneity when in fact it is not present. Conversely, ostensibly more accurate ‘second-order’ weights can dramatically increase the chances of failing to detect heterogeneity when it is truly present. We derive modified weights to mitigate both of these adverse effects. RESULTS: Using Monte Carlo simulations, we show that the modified weights outperform first- and second-order weights in terms of heterogeneity quantification. Modified weights are also shown to remove the phenomenon of regression dilution bias in MR estimates obtained from weak instruments, unlike those obtained using first- and second-order weights. However, with small numbers of weak instruments, this comes at the cost of a reduction in estimate precision and power to detect a causal effect compared with first-order weighting. Moreover, first-order weights always furnish unbiased estimates and preserve the type I error rate under the causal null. We illustrate the utility of the new method using data from a recent two-sample summary-data MR analysis to assess the causal role of systolic blood pressure on coronary heart disease risk. CONCLUSIONS: We propose the use of modified weights within two-sample summary-data MR studies for accurately quantifying heterogeneity and detecting outliers in the presence of weak instruments. Modified weights also have an important role to play in terms of causal estimation (in tandem with first-order weights) but further research is required to understand their strengths and weaknesses in specific settings.
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spelling pubmed-66593762019-08-02 Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption Bowden, Jack Del Greco M, Fabiola Minelli, Cosetta Zhao, Qingyuan Lawlor, Debbie A Sheehan, Nuala A Thompson, John Davey Smith, George Int J Epidemiol Mendelian Randomization BACKGROUND: Two-sample summary-data Mendelian randomization (MR) incorporating multiple genetic variants within a meta-analysis framework is a popular technique for assessing causality in epidemiology. If all genetic variants satisfy the instrumental variable (IV) and necessary modelling assumptions, then their individual ratio estimates of causal effect should be homogeneous. Observed heterogeneity signals that one or more of these assumptions could have been violated. METHODS: Causal estimation and heterogeneity assessment in MR require an approximation for the variance, or equivalently the inverse-variance weight, of each ratio estimate. We show that the most popular ‘first-order’ weights can lead to an inflation in the chances of detecting heterogeneity when in fact it is not present. Conversely, ostensibly more accurate ‘second-order’ weights can dramatically increase the chances of failing to detect heterogeneity when it is truly present. We derive modified weights to mitigate both of these adverse effects. RESULTS: Using Monte Carlo simulations, we show that the modified weights outperform first- and second-order weights in terms of heterogeneity quantification. Modified weights are also shown to remove the phenomenon of regression dilution bias in MR estimates obtained from weak instruments, unlike those obtained using first- and second-order weights. However, with small numbers of weak instruments, this comes at the cost of a reduction in estimate precision and power to detect a causal effect compared with first-order weighting. Moreover, first-order weights always furnish unbiased estimates and preserve the type I error rate under the causal null. We illustrate the utility of the new method using data from a recent two-sample summary-data MR analysis to assess the causal role of systolic blood pressure on coronary heart disease risk. CONCLUSIONS: We propose the use of modified weights within two-sample summary-data MR studies for accurately quantifying heterogeneity and detecting outliers in the presence of weak instruments. Modified weights also have an important role to play in terms of causal estimation (in tandem with first-order weights) but further research is required to understand their strengths and weaknesses in specific settings. Oxford University Press 2019-06 2018-12-18 /pmc/articles/PMC6659376/ /pubmed/30561657 http://dx.doi.org/10.1093/ije/dyy258 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the International Epidemiological Association. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Mendelian Randomization
Bowden, Jack
Del Greco M, Fabiola
Minelli, Cosetta
Zhao, Qingyuan
Lawlor, Debbie A
Sheehan, Nuala A
Thompson, John
Davey Smith, George
Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
title Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
title_full Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
title_fullStr Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
title_full_unstemmed Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
title_short Improving the accuracy of two-sample summary-data Mendelian randomization: moving beyond the NOME assumption
title_sort improving the accuracy of two-sample summary-data mendelian randomization: moving beyond the nome assumption
topic Mendelian Randomization
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659376/
https://www.ncbi.nlm.nih.gov/pubmed/30561657
http://dx.doi.org/10.1093/ije/dyy258
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