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Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components

BACKGROUND: Quantitative traits often underlie risk for complex diseases. For example, weight and body mass index (BMI) underlie the human abdominal obesity-metabolic syndrome. Many attempts have been made to identify quantitative trait loci (QTL) over the past decade, including association studies....

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Autores principales: Mei, Hao, Chen, Wei, Dellinger, Andrew, He, Jiang, Wang, Meng, Yau, Canddy, Srinivasan, Sathanur R, Berenson, Gerald S
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991276/
https://www.ncbi.nlm.nih.gov/pubmed/21062472
http://dx.doi.org/10.1186/1471-2156-11-100
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author Mei, Hao
Chen, Wei
Dellinger, Andrew
He, Jiang
Wang, Meng
Yau, Canddy
Srinivasan, Sathanur R
Berenson, Gerald S
author_facet Mei, Hao
Chen, Wei
Dellinger, Andrew
He, Jiang
Wang, Meng
Yau, Canddy
Srinivasan, Sathanur R
Berenson, Gerald S
author_sort Mei, Hao
collection PubMed
description BACKGROUND: Quantitative traits often underlie risk for complex diseases. For example, weight and body mass index (BMI) underlie the human abdominal obesity-metabolic syndrome. Many attempts have been made to identify quantitative trait loci (QTL) over the past decade, including association studies. However, a single QTL is often capable of affecting multiple traits, a quality known as gene pleiotropy. Gene pleiotropy may therefore cause a loss of power in association studies focused only on a single trait, whether based on single or multiple markers. RESULTS: We propose using principal-component-based multivariate regression (PCBMR) to test for gene pleiotropy with comprehensive evaluation. This method generates one or more independent canonical variables based on the principal components of original traits and conducts a multivariate regression to test for association with these new variables. Systematic simulation studies have shown that PCBMR has great power. PCBMR-based pleiotropic association studies of abdominal obesity-metabolic syndrome and its possible linkage to chromosomal band 3q27 identified 11 susceptibility genes with significant associations. Whereas some of these genes had been previously reported to be associated with metabolic traits, others had never been identified as metabolism-associated genes. CONCLUSIONS: PCBMR is a computationally efficient and powerful test for gene pleiotropy. Application of PCBMR to abdominal obesity-metabolic syndrome indicated the existence of gene pleiotropy affecting this syndrome.
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spelling pubmed-29912762010-12-13 Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components Mei, Hao Chen, Wei Dellinger, Andrew He, Jiang Wang, Meng Yau, Canddy Srinivasan, Sathanur R Berenson, Gerald S BMC Genet Methodology Article BACKGROUND: Quantitative traits often underlie risk for complex diseases. For example, weight and body mass index (BMI) underlie the human abdominal obesity-metabolic syndrome. Many attempts have been made to identify quantitative trait loci (QTL) over the past decade, including association studies. However, a single QTL is often capable of affecting multiple traits, a quality known as gene pleiotropy. Gene pleiotropy may therefore cause a loss of power in association studies focused only on a single trait, whether based on single or multiple markers. RESULTS: We propose using principal-component-based multivariate regression (PCBMR) to test for gene pleiotropy with comprehensive evaluation. This method generates one or more independent canonical variables based on the principal components of original traits and conducts a multivariate regression to test for association with these new variables. Systematic simulation studies have shown that PCBMR has great power. PCBMR-based pleiotropic association studies of abdominal obesity-metabolic syndrome and its possible linkage to chromosomal band 3q27 identified 11 susceptibility genes with significant associations. Whereas some of these genes had been previously reported to be associated with metabolic traits, others had never been identified as metabolism-associated genes. CONCLUSIONS: PCBMR is a computationally efficient and powerful test for gene pleiotropy. Application of PCBMR to abdominal obesity-metabolic syndrome indicated the existence of gene pleiotropy affecting this syndrome. BioMed Central 2010-11-09 /pmc/articles/PMC2991276/ /pubmed/21062472 http://dx.doi.org/10.1186/1471-2156-11-100 Text en Copyright ©2010 Mei et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methodology Article
Mei, Hao
Chen, Wei
Dellinger, Andrew
He, Jiang
Wang, Meng
Yau, Canddy
Srinivasan, Sathanur R
Berenson, Gerald S
Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components
title Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components
title_full Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components
title_fullStr Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components
title_full_unstemmed Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components
title_short Principal-component-based multivariate regression for genetic association studies of metabolic syndrome components
title_sort principal-component-based multivariate regression for genetic association studies of metabolic syndrome components
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2991276/
https://www.ncbi.nlm.nih.gov/pubmed/21062472
http://dx.doi.org/10.1186/1471-2156-11-100
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