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Constrained instruments and their application to Mendelian randomization with pleiotropy
In Mendelian randomization (MR), inference about causal relationship between a phenotype of interest and a response or disease outcome can be obtained by constructing instrumental variables from genetic variants. However, MR inference requires three assumptions, one of which is that the genetic vari...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537099/ https://www.ncbi.nlm.nih.gov/pubmed/30635941 http://dx.doi.org/10.1002/gepi.22184 |
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author | Jiang, Lai Oualkacha, Karim Didelez, Vanessa Ciampi, Antonio Rosa‐Neto, Pedro Benedet, Andrea L. Mathotaarachchi, Sulantha Richards, John Brent Greenwood, Celia M. T. |
author_facet | Jiang, Lai Oualkacha, Karim Didelez, Vanessa Ciampi, Antonio Rosa‐Neto, Pedro Benedet, Andrea L. Mathotaarachchi, Sulantha Richards, John Brent Greenwood, Celia M. T. |
author_sort | Jiang, Lai |
collection | PubMed |
description | In Mendelian randomization (MR), inference about causal relationship between a phenotype of interest and a response or disease outcome can be obtained by constructing instrumental variables from genetic variants. However, MR inference requires three assumptions, one of which is that the genetic variants only influence the outcome through phenotype of interest. Pleiotropy, that is, the situation in which some genetic variants affect more than one phenotype, can invalidate these genetic variants for use as instrumental variables; thus a naive analysis will give biased estimates of the causal relation. Here, we present new methods (constrained instrumental variable [CIV] methods) to construct valid instrumental variables and perform adjusted causal effect estimation when pleiotropy exists and when the pleiotropic phenotypes are available. We demonstrate that a smoothed version of CIV performs approximate selection of genetic variants that are valid instruments, and provides unbiased estimates of the causal effects. We provide details on a number of existing methods, together with a comparison of their performance in a large series of simulations. CIV performs robustly across different pleiotropic violations of the MR assumptions. We also analyzed the data from the Alzheimer’s disease (AD) neuroimaging initiative (ADNI; Mueller et al., 2005. Alzheimer's Dementia, 11(1), 55–66) to disentangle causal relationships of several biomarkers with AD progression. |
format | Online Article Text |
id | pubmed-6537099 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65370992019-06-01 Constrained instruments and their application to Mendelian randomization with pleiotropy Jiang, Lai Oualkacha, Karim Didelez, Vanessa Ciampi, Antonio Rosa‐Neto, Pedro Benedet, Andrea L. Mathotaarachchi, Sulantha Richards, John Brent Greenwood, Celia M. T. Genet Epidemiol Research Articles In Mendelian randomization (MR), inference about causal relationship between a phenotype of interest and a response or disease outcome can be obtained by constructing instrumental variables from genetic variants. However, MR inference requires three assumptions, one of which is that the genetic variants only influence the outcome through phenotype of interest. Pleiotropy, that is, the situation in which some genetic variants affect more than one phenotype, can invalidate these genetic variants for use as instrumental variables; thus a naive analysis will give biased estimates of the causal relation. Here, we present new methods (constrained instrumental variable [CIV] methods) to construct valid instrumental variables and perform adjusted causal effect estimation when pleiotropy exists and when the pleiotropic phenotypes are available. We demonstrate that a smoothed version of CIV performs approximate selection of genetic variants that are valid instruments, and provides unbiased estimates of the causal effects. We provide details on a number of existing methods, together with a comparison of their performance in a large series of simulations. CIV performs robustly across different pleiotropic violations of the MR assumptions. We also analyzed the data from the Alzheimer’s disease (AD) neuroimaging initiative (ADNI; Mueller et al., 2005. Alzheimer's Dementia, 11(1), 55–66) to disentangle causal relationships of several biomarkers with AD progression. John Wiley and Sons Inc. 2019-01-12 2019-06 /pmc/articles/PMC6537099/ /pubmed/30635941 http://dx.doi.org/10.1002/gepi.22184 Text en © 2019 The Authors. Genetic Epidemiology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Jiang, Lai Oualkacha, Karim Didelez, Vanessa Ciampi, Antonio Rosa‐Neto, Pedro Benedet, Andrea L. Mathotaarachchi, Sulantha Richards, John Brent Greenwood, Celia M. T. Constrained instruments and their application to Mendelian randomization with pleiotropy |
title | Constrained instruments and their application to Mendelian randomization with pleiotropy |
title_full | Constrained instruments and their application to Mendelian randomization with pleiotropy |
title_fullStr | Constrained instruments and their application to Mendelian randomization with pleiotropy |
title_full_unstemmed | Constrained instruments and their application to Mendelian randomization with pleiotropy |
title_short | Constrained instruments and their application to Mendelian randomization with pleiotropy |
title_sort | constrained instruments and their application to mendelian randomization with pleiotropy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6537099/ https://www.ncbi.nlm.nih.gov/pubmed/30635941 http://dx.doi.org/10.1002/gepi.22184 |
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