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Optimized Phenotypic Biomarker Discovery and Confounder Elimination via Covariate-Adjusted Projection to Latent Structures from Metabolic Spectroscopy Data
[Image: see text] Metabolism is altered by genetics, diet, disease status, environment, and many other factors. Modeling either one of these is often done without considering the effects of the other covariates. Attributing differences in metabolic profile to one of these factors needs to be done wh...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891819/ https://www.ncbi.nlm.nih.gov/pubmed/29457906 http://dx.doi.org/10.1021/acs.jproteome.7b00879 |
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author | Posma, Joram M. Garcia-Perez, Isabel Ebbels, Timothy M. D. Lindon, John C. Stamler, Jeremiah Elliott, Paul Holmes, Elaine Nicholson, Jeremy K. |
author_facet | Posma, Joram M. Garcia-Perez, Isabel Ebbels, Timothy M. D. Lindon, John C. Stamler, Jeremiah Elliott, Paul Holmes, Elaine Nicholson, Jeremy K. |
author_sort | Posma, Joram M. |
collection | PubMed |
description | [Image: see text] Metabolism is altered by genetics, diet, disease status, environment, and many other factors. Modeling either one of these is often done without considering the effects of the other covariates. Attributing differences in metabolic profile to one of these factors needs to be done while controlling for the metabolic influence of the rest. We describe here a data analysis framework and novel confounder-adjustment algorithm for multivariate analysis of metabolic profiling data. Using simulated data, we show that similar numbers of true associations and significantly less false positives are found compared to other commonly used methods. Covariate-adjusted projections to latent structures (CA-PLS) are exemplified here using a large-scale metabolic phenotyping study of two Chinese populations at different risks for cardiovascular disease. Using CA-PLS, we find that some previously reported differences are actually associated with external factors and discover a number of previously unreported biomarkers linked to different metabolic pathways. CA-PLS can be applied to any multivariate data where confounding may be an issue and the confounder-adjustment procedure is translatable to other multivariate regression techniques. |
format | Online Article Text |
id | pubmed-5891819 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-58918192018-04-11 Optimized Phenotypic Biomarker Discovery and Confounder Elimination via Covariate-Adjusted Projection to Latent Structures from Metabolic Spectroscopy Data Posma, Joram M. Garcia-Perez, Isabel Ebbels, Timothy M. D. Lindon, John C. Stamler, Jeremiah Elliott, Paul Holmes, Elaine Nicholson, Jeremy K. J Proteome Res [Image: see text] Metabolism is altered by genetics, diet, disease status, environment, and many other factors. Modeling either one of these is often done without considering the effects of the other covariates. Attributing differences in metabolic profile to one of these factors needs to be done while controlling for the metabolic influence of the rest. We describe here a data analysis framework and novel confounder-adjustment algorithm for multivariate analysis of metabolic profiling data. Using simulated data, we show that similar numbers of true associations and significantly less false positives are found compared to other commonly used methods. Covariate-adjusted projections to latent structures (CA-PLS) are exemplified here using a large-scale metabolic phenotyping study of two Chinese populations at different risks for cardiovascular disease. Using CA-PLS, we find that some previously reported differences are actually associated with external factors and discover a number of previously unreported biomarkers linked to different metabolic pathways. CA-PLS can be applied to any multivariate data where confounding may be an issue and the confounder-adjustment procedure is translatable to other multivariate regression techniques. American Chemical Society 2018-02-19 2018-04-06 /pmc/articles/PMC5891819/ /pubmed/29457906 http://dx.doi.org/10.1021/acs.jproteome.7b00879 Text en Copyright © 2018 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Posma, Joram M. Garcia-Perez, Isabel Ebbels, Timothy M. D. Lindon, John C. Stamler, Jeremiah Elliott, Paul Holmes, Elaine Nicholson, Jeremy K. Optimized Phenotypic Biomarker Discovery and Confounder Elimination via Covariate-Adjusted Projection to Latent Structures from Metabolic Spectroscopy Data |
title | Optimized Phenotypic
Biomarker Discovery and Confounder
Elimination via Covariate-Adjusted Projection to Latent Structures
from Metabolic Spectroscopy Data |
title_full | Optimized Phenotypic
Biomarker Discovery and Confounder
Elimination via Covariate-Adjusted Projection to Latent Structures
from Metabolic Spectroscopy Data |
title_fullStr | Optimized Phenotypic
Biomarker Discovery and Confounder
Elimination via Covariate-Adjusted Projection to Latent Structures
from Metabolic Spectroscopy Data |
title_full_unstemmed | Optimized Phenotypic
Biomarker Discovery and Confounder
Elimination via Covariate-Adjusted Projection to Latent Structures
from Metabolic Spectroscopy Data |
title_short | Optimized Phenotypic
Biomarker Discovery and Confounder
Elimination via Covariate-Adjusted Projection to Latent Structures
from Metabolic Spectroscopy Data |
title_sort | optimized phenotypic
biomarker discovery and confounder
elimination via covariate-adjusted projection to latent structures
from metabolic spectroscopy data |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5891819/ https://www.ncbi.nlm.nih.gov/pubmed/29457906 http://dx.doi.org/10.1021/acs.jproteome.7b00879 |
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