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Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations

In genetic association studies, it is important to distinguish direct and indirect genetic effects in order to build truly functional models. For this purpose, we consider a directed acyclic graph setting with genetic variants, primary and intermediate phenotypes, and confounding factors. In order t...

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Autores principales: Konigorski, Stefan, Wang, Yuan, Cigsar, Candemir, Yilmaz, Yildiz E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619348/
https://www.ncbi.nlm.nih.gov/pubmed/29265408
http://dx.doi.org/10.1002/gepi.22107
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author Konigorski, Stefan
Wang, Yuan
Cigsar, Candemir
Yilmaz, Yildiz E.
author_facet Konigorski, Stefan
Wang, Yuan
Cigsar, Candemir
Yilmaz, Yildiz E.
author_sort Konigorski, Stefan
collection PubMed
description In genetic association studies, it is important to distinguish direct and indirect genetic effects in order to build truly functional models. For this purpose, we consider a directed acyclic graph setting with genetic variants, primary and intermediate phenotypes, and confounding factors. In order to make valid statistical inference on direct genetic effects on the primary phenotype, it is necessary to consider all potential effects in the graph, and we propose to use the estimating equations method with robust Huber–White sandwich standard errors. We evaluate the proposed causal inference based on estimating equations (CIEE) method and compare it with traditional multiple regression methods, the structural equation modeling method, and sequential G‐estimation methods through a simulation study for the analysis of (completely observed) quantitative traits and time‐to‐event traits subject to censoring as primary phenotypes. The results show that CIEE provides valid estimators and inference by successfully removing the effect of intermediate phenotypes from the primary phenotype and is robust against measured and unmeasured confounding of the indirect effect through observed factors. All other methods except the sequential G‐estimation method for quantitative traits fail in some scenarios where their test statistics yield inflated type I errors. In the analysis of the Genetic Analysis Workshop 19 dataset, we estimate and test genetic effects on blood pressure accounting for intermediate gene expression phenotypes. The results show that CIEE can identify genetic variants that would be missed by traditional regression analyses. CIEE is computationally fast, widely applicable to different fields, and available as an R package.
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spelling pubmed-66193482019-07-22 Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations Konigorski, Stefan Wang, Yuan Cigsar, Candemir Yilmaz, Yildiz E. Genet Epidemiol Research Articles In genetic association studies, it is important to distinguish direct and indirect genetic effects in order to build truly functional models. For this purpose, we consider a directed acyclic graph setting with genetic variants, primary and intermediate phenotypes, and confounding factors. In order to make valid statistical inference on direct genetic effects on the primary phenotype, it is necessary to consider all potential effects in the graph, and we propose to use the estimating equations method with robust Huber–White sandwich standard errors. We evaluate the proposed causal inference based on estimating equations (CIEE) method and compare it with traditional multiple regression methods, the structural equation modeling method, and sequential G‐estimation methods through a simulation study for the analysis of (completely observed) quantitative traits and time‐to‐event traits subject to censoring as primary phenotypes. The results show that CIEE provides valid estimators and inference by successfully removing the effect of intermediate phenotypes from the primary phenotype and is robust against measured and unmeasured confounding of the indirect effect through observed factors. All other methods except the sequential G‐estimation method for quantitative traits fail in some scenarios where their test statistics yield inflated type I errors. In the analysis of the Genetic Analysis Workshop 19 dataset, we estimate and test genetic effects on blood pressure accounting for intermediate gene expression phenotypes. The results show that CIEE can identify genetic variants that would be missed by traditional regression analyses. CIEE is computationally fast, widely applicable to different fields, and available as an R package. John Wiley and Sons Inc. 2017-12-18 2018-03 /pmc/articles/PMC6619348/ /pubmed/29265408 http://dx.doi.org/10.1002/gepi.22107 Text en © 2017 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-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Konigorski, Stefan
Wang, Yuan
Cigsar, Candemir
Yilmaz, Yildiz E.
Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
title Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
title_full Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
title_fullStr Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
title_full_unstemmed Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
title_short Estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
title_sort estimating and testing direct genetic effects in directed acyclic graphs using estimating equations
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6619348/
https://www.ncbi.nlm.nih.gov/pubmed/29265408
http://dx.doi.org/10.1002/gepi.22107
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