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A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits

Genetic pleiotropy refers to the situation in which a single gene influences multiple traits and so it is considered as a major factor that underlies genetic correlation among traits. To identify pleiotropy, an important focus in genome-wide association studies (GWAS) is on finding genetic variants...

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Autores principales: Wang, Weiqiang, Feng, Zeny, Bull, Shelley B., Wang, Zuoheng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202779/
https://www.ncbi.nlm.nih.gov/pubmed/25368629
http://dx.doi.org/10.3389/fgene.2014.00357
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author Wang, Weiqiang
Feng, Zeny
Bull, Shelley B.
Wang, Zuoheng
author_facet Wang, Weiqiang
Feng, Zeny
Bull, Shelley B.
Wang, Zuoheng
author_sort Wang, Weiqiang
collection PubMed
description Genetic pleiotropy refers to the situation in which a single gene influences multiple traits and so it is considered as a major factor that underlies genetic correlation among traits. To identify pleiotropy, an important focus in genome-wide association studies (GWAS) is on finding genetic variants that are simultaneously associated with multiple traits. On the other hand, longitudinal designs are often employed in many complex disease studies, such that, traits are measured repeatedly over time within the same subject. Performing genetic association analysis simultaneously on multiple longitudinal traits for detecting pleiotropic effects is interesting but challenging. In this paper, we propose a 2-step method for simultaneously testing the genetic association with multiple longitudinal traits. In the first step, a mixed effects model is used to analyze each longitudinal trait. We focus on estimation of the random effect that accounts for the subject-specific genetic contribution to the trait; fixed effects of other confounding covariates are also estimated. This first step enables separation of the genetic effect from other confounding effects for each subject and for each longitudinal trait. Then in the second step, we perform a simultaneous association test on multiple estimated random effects arising from multiple longitudinal traits. The proposed method can efficiently detect pleiotropic effects on multiple longitudinal traits and can flexibly handle traits of different data types such as quantitative, binary, or count data. We apply this method to analyze the 16th Genetic Analysis Workshop (GAW16) Framingham Heart Study (FHS) data. A simulation study is also conducted to validate this 2-step method and evaluate its performance.
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spelling pubmed-42027792014-11-03 A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits Wang, Weiqiang Feng, Zeny Bull, Shelley B. Wang, Zuoheng Front Genet Genetics Genetic pleiotropy refers to the situation in which a single gene influences multiple traits and so it is considered as a major factor that underlies genetic correlation among traits. To identify pleiotropy, an important focus in genome-wide association studies (GWAS) is on finding genetic variants that are simultaneously associated with multiple traits. On the other hand, longitudinal designs are often employed in many complex disease studies, such that, traits are measured repeatedly over time within the same subject. Performing genetic association analysis simultaneously on multiple longitudinal traits for detecting pleiotropic effects is interesting but challenging. In this paper, we propose a 2-step method for simultaneously testing the genetic association with multiple longitudinal traits. In the first step, a mixed effects model is used to analyze each longitudinal trait. We focus on estimation of the random effect that accounts for the subject-specific genetic contribution to the trait; fixed effects of other confounding covariates are also estimated. This first step enables separation of the genetic effect from other confounding effects for each subject and for each longitudinal trait. Then in the second step, we perform a simultaneous association test on multiple estimated random effects arising from multiple longitudinal traits. The proposed method can efficiently detect pleiotropic effects on multiple longitudinal traits and can flexibly handle traits of different data types such as quantitative, binary, or count data. We apply this method to analyze the 16th Genetic Analysis Workshop (GAW16) Framingham Heart Study (FHS) data. A simulation study is also conducted to validate this 2-step method and evaluate its performance. Frontiers Media S.A. 2014-10-20 /pmc/articles/PMC4202779/ /pubmed/25368629 http://dx.doi.org/10.3389/fgene.2014.00357 Text en Copyright © 2014 Wang, Feng, Bull and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Genetics
Wang, Weiqiang
Feng, Zeny
Bull, Shelley B.
Wang, Zuoheng
A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
title A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
title_full A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
title_fullStr A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
title_full_unstemmed A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
title_short A 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
title_sort 2-step strategy for detecting pleiotropic effects on multiple longitudinal traits
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4202779/
https://www.ncbi.nlm.nih.gov/pubmed/25368629
http://dx.doi.org/10.3389/fgene.2014.00357
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