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A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study

Genetic association studies are now routinely used to identify single nucleotide polymorphisms (SNPs) linked with human diseases or traits through single SNP-single trait tests. Here we introduced partial least squares path modeling (PLSPM) for association between single or multiple SNPs and a laten...

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Autores principales: Xue, Fuzhong, Li, Shengxu, Luan, Jian'an, Yuan, Zhongshang, Luben, Robert N., Khaw, Kay-Tee, Wareham, Nicholas J., Loos, Ruth J. F., Zhao, Jing Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288051/
https://www.ncbi.nlm.nih.gov/pubmed/22384102
http://dx.doi.org/10.1371/journal.pone.0031927
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author Xue, Fuzhong
Li, Shengxu
Luan, Jian'an
Yuan, Zhongshang
Luben, Robert N.
Khaw, Kay-Tee
Wareham, Nicholas J.
Loos, Ruth J. F.
Zhao, Jing Hua
author_facet Xue, Fuzhong
Li, Shengxu
Luan, Jian'an
Yuan, Zhongshang
Luben, Robert N.
Khaw, Kay-Tee
Wareham, Nicholas J.
Loos, Ruth J. F.
Zhao, Jing Hua
author_sort Xue, Fuzhong
collection PubMed
description Genetic association studies are now routinely used to identify single nucleotide polymorphisms (SNPs) linked with human diseases or traits through single SNP-single trait tests. Here we introduced partial least squares path modeling (PLSPM) for association between single or multiple SNPs and a latent trait that can involve single or multiple correlated measurement(s). Furthermore, the framework naturally provides estimators of polygenic effect by appropriately weighting trait-attributing alleles. We conducted computer simulations to assess the performance via multiple SNPs and human obesity-related traits as measured by body mass index (BMI), waist and hip circumferences. Our results showed that the associate statistics had type I error rates close to nominal level and were powerful for a range of effect and sample sizes. When applied to 12 candidate regions in data (N = 2,417) from the European Prospective Investigation of Cancer (EPIC)-Norfolk study, a region in FTO was found to have stronger association (rs7204609∼rs9939881 at the first intron P = 4.29×10(−7)) than single SNP analysis (all with P>10(−4)) and a latent quantitative phenotype was obtained using a subset sample of EPIC-Norfolk (N = 12,559). We believe our method is appropriate for assessment of regional association and polygenic effect on a single or multiple traits.
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spelling pubmed-32880512012-03-01 A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study Xue, Fuzhong Li, Shengxu Luan, Jian'an Yuan, Zhongshang Luben, Robert N. Khaw, Kay-Tee Wareham, Nicholas J. Loos, Ruth J. F. Zhao, Jing Hua PLoS One Research Article Genetic association studies are now routinely used to identify single nucleotide polymorphisms (SNPs) linked with human diseases or traits through single SNP-single trait tests. Here we introduced partial least squares path modeling (PLSPM) for association between single or multiple SNPs and a latent trait that can involve single or multiple correlated measurement(s). Furthermore, the framework naturally provides estimators of polygenic effect by appropriately weighting trait-attributing alleles. We conducted computer simulations to assess the performance via multiple SNPs and human obesity-related traits as measured by body mass index (BMI), waist and hip circumferences. Our results showed that the associate statistics had type I error rates close to nominal level and were powerful for a range of effect and sample sizes. When applied to 12 candidate regions in data (N = 2,417) from the European Prospective Investigation of Cancer (EPIC)-Norfolk study, a region in FTO was found to have stronger association (rs7204609∼rs9939881 at the first intron P = 4.29×10(−7)) than single SNP analysis (all with P>10(−4)) and a latent quantitative phenotype was obtained using a subset sample of EPIC-Norfolk (N = 12,559). We believe our method is appropriate for assessment of regional association and polygenic effect on a single or multiple traits. Public Library of Science 2012-02-27 /pmc/articles/PMC3288051/ /pubmed/22384102 http://dx.doi.org/10.1371/journal.pone.0031927 Text en Xue et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Xue, Fuzhong
Li, Shengxu
Luan, Jian'an
Yuan, Zhongshang
Luben, Robert N.
Khaw, Kay-Tee
Wareham, Nicholas J.
Loos, Ruth J. F.
Zhao, Jing Hua
A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
title A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
title_full A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
title_fullStr A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
title_full_unstemmed A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
title_short A Latent Variable Partial Least Squares Path Modeling Approach to Regional Association and Polygenic Effect with Applications to a Human Obesity Study
title_sort latent variable partial least squares path modeling approach to regional association and polygenic effect with applications to a human obesity study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3288051/
https://www.ncbi.nlm.nih.gov/pubmed/22384102
http://dx.doi.org/10.1371/journal.pone.0031927
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