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A classification modeling approach for determining metabolite signatures in osteoarthritis
Multiple factors can help predict knee osteoarthritis (OA) patients from healthy individuals, including age, sex, and BMI, and possibly metabolite levels. Using plasma from individuals with primary OA undergoing total knee replacement and healthy volunteers, we measured lysophosphatidylcholine (lyso...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025859/ https://www.ncbi.nlm.nih.gov/pubmed/29958292 http://dx.doi.org/10.1371/journal.pone.0199618 |
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author | Rockel, Jason S. Zhang, Weidong Shestopaloff, Konstantin Likhodii, Sergei Sun, Guang Furey, Andrew Randell, Edward Sundararajan, Kala Gandhi, Rajiv Zhai, Guangju Kapoor, Mohit |
author_facet | Rockel, Jason S. Zhang, Weidong Shestopaloff, Konstantin Likhodii, Sergei Sun, Guang Furey, Andrew Randell, Edward Sundararajan, Kala Gandhi, Rajiv Zhai, Guangju Kapoor, Mohit |
author_sort | Rockel, Jason S. |
collection | PubMed |
description | Multiple factors can help predict knee osteoarthritis (OA) patients from healthy individuals, including age, sex, and BMI, and possibly metabolite levels. Using plasma from individuals with primary OA undergoing total knee replacement and healthy volunteers, we measured lysophosphatidylcholine (lysoPC) and phosphatidylcholine (PC) analogues by metabolomics. Populations were stratified on demographic factors and lysoPC and PC analogue signatures were determined by univariate receiver-operator curve (AUC) analysis. Using signatures, multivariate classification modeling was performed using various algorithms to select the most consistent method as measured by AUC differences between resampled training and test sets. Lists of metabolites indicative of OA [AUC > 0.5] were identified for each stratum. The signature from males age > 50 years old encompassed the majority of identified metabolites, suggesting lysoPCs and PCs are dominant indicators of OA in older males. Principal component regression with logistic regression was the most consistent multivariate classification algorithm tested. Using this algorithm, classification of older males had fair power to classify OA patients from healthy individuals. Thus, individual levels of lysoPC and PC analogues may be indicative of individuals with OA in older populations, particularly males. Our metabolite signature modeling method is likely to increase classification power in validation cohorts. |
format | Online Article Text |
id | pubmed-6025859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-60258592018-07-07 A classification modeling approach for determining metabolite signatures in osteoarthritis Rockel, Jason S. Zhang, Weidong Shestopaloff, Konstantin Likhodii, Sergei Sun, Guang Furey, Andrew Randell, Edward Sundararajan, Kala Gandhi, Rajiv Zhai, Guangju Kapoor, Mohit PLoS One Research Article Multiple factors can help predict knee osteoarthritis (OA) patients from healthy individuals, including age, sex, and BMI, and possibly metabolite levels. Using plasma from individuals with primary OA undergoing total knee replacement and healthy volunteers, we measured lysophosphatidylcholine (lysoPC) and phosphatidylcholine (PC) analogues by metabolomics. Populations were stratified on demographic factors and lysoPC and PC analogue signatures were determined by univariate receiver-operator curve (AUC) analysis. Using signatures, multivariate classification modeling was performed using various algorithms to select the most consistent method as measured by AUC differences between resampled training and test sets. Lists of metabolites indicative of OA [AUC > 0.5] were identified for each stratum. The signature from males age > 50 years old encompassed the majority of identified metabolites, suggesting lysoPCs and PCs are dominant indicators of OA in older males. Principal component regression with logistic regression was the most consistent multivariate classification algorithm tested. Using this algorithm, classification of older males had fair power to classify OA patients from healthy individuals. Thus, individual levels of lysoPC and PC analogues may be indicative of individuals with OA in older populations, particularly males. Our metabolite signature modeling method is likely to increase classification power in validation cohorts. Public Library of Science 2018-06-29 /pmc/articles/PMC6025859/ /pubmed/29958292 http://dx.doi.org/10.1371/journal.pone.0199618 Text en © 2018 Rockel 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Rockel, Jason S. Zhang, Weidong Shestopaloff, Konstantin Likhodii, Sergei Sun, Guang Furey, Andrew Randell, Edward Sundararajan, Kala Gandhi, Rajiv Zhai, Guangju Kapoor, Mohit A classification modeling approach for determining metabolite signatures in osteoarthritis |
title | A classification modeling approach for determining metabolite signatures in osteoarthritis |
title_full | A classification modeling approach for determining metabolite signatures in osteoarthritis |
title_fullStr | A classification modeling approach for determining metabolite signatures in osteoarthritis |
title_full_unstemmed | A classification modeling approach for determining metabolite signatures in osteoarthritis |
title_short | A classification modeling approach for determining metabolite signatures in osteoarthritis |
title_sort | classification modeling approach for determining metabolite signatures in osteoarthritis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6025859/ https://www.ncbi.nlm.nih.gov/pubmed/29958292 http://dx.doi.org/10.1371/journal.pone.0199618 |
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