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Use of allele scores as instrumental variables for Mendelian randomization
Background An allele score is a single variable summarizing multiple genetic variants associated with a risk factor. It is calculated as the total number of risk factor-increasing alleles for an individual (unweighted score), or the sum of weights for each allele corresponding to estimated genetic e...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2013
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3780999/ https://www.ncbi.nlm.nih.gov/pubmed/24062299 http://dx.doi.org/10.1093/ije/dyt093 |
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author | Burgess, Stephen Thompson, Simon G |
author_facet | Burgess, Stephen Thompson, Simon G |
author_sort | Burgess, Stephen |
collection | PubMed |
description | Background An allele score is a single variable summarizing multiple genetic variants associated with a risk factor. It is calculated as the total number of risk factor-increasing alleles for an individual (unweighted score), or the sum of weights for each allele corresponding to estimated genetic effect sizes (weighted score). An allele score can be used in a Mendelian randomization analysis to estimate the causal effect of the risk factor on an outcome. Methods Data were simulated to investigate the use of allele scores in Mendelian randomization where conventional instrumental variable techniques using multiple genetic variants demonstrate ‘weak instrument’ bias. The robustness of estimates using the allele score to misspecification (for example non-linearity, effect modification) and to violations of the instrumental variable assumptions was assessed. Results Causal estimates using a correctly specified allele score were unbiased with appropriate coverage levels. The estimates were generally robust to misspecification of the allele score, but not to instrumental variable violations, even if the majority of variants in the allele score were valid instruments. Using a weighted rather than an unweighted allele score increased power, but the increase was small when genetic variants had similar effect sizes. Naive use of the data under analysis to choose which variants to include in an allele score, or for deriving weights, resulted in substantial biases. Conclusions Allele scores enable valid causal estimates with large numbers of genetic variants. The stringency of criteria for genetic variants in Mendelian randomization should be maintained for all variants in an allele score. |
format | Online Article Text |
id | pubmed-3780999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-37809992013-09-24 Use of allele scores as instrumental variables for Mendelian randomization Burgess, Stephen Thompson, Simon G Int J Epidemiol Methodology Background An allele score is a single variable summarizing multiple genetic variants associated with a risk factor. It is calculated as the total number of risk factor-increasing alleles for an individual (unweighted score), or the sum of weights for each allele corresponding to estimated genetic effect sizes (weighted score). An allele score can be used in a Mendelian randomization analysis to estimate the causal effect of the risk factor on an outcome. Methods Data were simulated to investigate the use of allele scores in Mendelian randomization where conventional instrumental variable techniques using multiple genetic variants demonstrate ‘weak instrument’ bias. The robustness of estimates using the allele score to misspecification (for example non-linearity, effect modification) and to violations of the instrumental variable assumptions was assessed. Results Causal estimates using a correctly specified allele score were unbiased with appropriate coverage levels. The estimates were generally robust to misspecification of the allele score, but not to instrumental variable violations, even if the majority of variants in the allele score were valid instruments. Using a weighted rather than an unweighted allele score increased power, but the increase was small when genetic variants had similar effect sizes. Naive use of the data under analysis to choose which variants to include in an allele score, or for deriving weights, resulted in substantial biases. Conclusions Allele scores enable valid causal estimates with large numbers of genetic variants. The stringency of criteria for genetic variants in Mendelian randomization should be maintained for all variants in an allele score. Oxford University Press 2013-08 2013-08-30 /pmc/articles/PMC3780999/ /pubmed/24062299 http://dx.doi.org/10.1093/ije/dyt093 Text en Published by Oxford University Press on behalf of the International Epidemiological Association © The Author 2013. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methodology Burgess, Stephen Thompson, Simon G Use of allele scores as instrumental variables for Mendelian randomization |
title | Use of allele scores as instrumental variables for Mendelian randomization |
title_full | Use of allele scores as instrumental variables for Mendelian randomization |
title_fullStr | Use of allele scores as instrumental variables for Mendelian randomization |
title_full_unstemmed | Use of allele scores as instrumental variables for Mendelian randomization |
title_short | Use of allele scores as instrumental variables for Mendelian randomization |
title_sort | use of allele scores as instrumental variables for mendelian randomization |
topic | Methodology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3780999/ https://www.ncbi.nlm.nih.gov/pubmed/24062299 http://dx.doi.org/10.1093/ije/dyt093 |
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