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Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals

Chronic obstructive pulmonary disease (COPD) has seriously impacted the health of individuals and populations. In this study, proton nuclear magnetic resonance ((1)H NMR)-based metabonomics combined with multivariate pattern recognition analysis was applied to investigate the metabolic signatures of...

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Autores principales: Wang, Lingling, Tang, Yufu, Liu, Shuo, Mao, Shitao, Ling, Yuan, Liu, Dan, He, Xiaoyu, Wang, Xiaoge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675021/
https://www.ncbi.nlm.nih.gov/pubmed/23755267
http://dx.doi.org/10.1371/journal.pone.0065675
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author Wang, Lingling
Tang, Yufu
Liu, Shuo
Mao, Shitao
Ling, Yuan
Liu, Dan
He, Xiaoyu
Wang, Xiaoge
author_facet Wang, Lingling
Tang, Yufu
Liu, Shuo
Mao, Shitao
Ling, Yuan
Liu, Dan
He, Xiaoyu
Wang, Xiaoge
author_sort Wang, Lingling
collection PubMed
description Chronic obstructive pulmonary disease (COPD) has seriously impacted the health of individuals and populations. In this study, proton nuclear magnetic resonance ((1)H NMR)-based metabonomics combined with multivariate pattern recognition analysis was applied to investigate the metabolic signatures of patients with COPD. Serum and urine samples were collected from COPD patients (n = 32) and healthy controls (n = 21), respectively. Samples were analyzed by high resolution (1)H NMR (600 MHz), and the obtained spectral profiles were then subjected to multivariate data analysis. Consistent metabolic differences have been found in serum as well as in urine samples from COPD patients and healthy controls. Compared to healthy controls, COPD patients displayed decreased lipoprotein and amino acids, including branched-chain amino acids (BCAAs), and increased glycerolphosphocholine in serum. Moreover, metabolic differences in urine were more significant than in serum. Decreased urinary 1-methylnicotinamide, creatinine and lactate have been discovered in COPD patients in comparison with healthy controls. Conversely, acetate, ketone bodies, carnosine, m-hydroxyphenylacetate, phenylacetyglycine, pyruvate and α-ketoglutarate exhibited enhanced expression levels in COPD patients relative to healthy subjects. Our results illustrate the potential application of NMR-based metabonomics in early diagnosis and understanding the mechanisms of COPD.
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spelling pubmed-36750212013-06-10 Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals Wang, Lingling Tang, Yufu Liu, Shuo Mao, Shitao Ling, Yuan Liu, Dan He, Xiaoyu Wang, Xiaoge PLoS One Research Article Chronic obstructive pulmonary disease (COPD) has seriously impacted the health of individuals and populations. In this study, proton nuclear magnetic resonance ((1)H NMR)-based metabonomics combined with multivariate pattern recognition analysis was applied to investigate the metabolic signatures of patients with COPD. Serum and urine samples were collected from COPD patients (n = 32) and healthy controls (n = 21), respectively. Samples were analyzed by high resolution (1)H NMR (600 MHz), and the obtained spectral profiles were then subjected to multivariate data analysis. Consistent metabolic differences have been found in serum as well as in urine samples from COPD patients and healthy controls. Compared to healthy controls, COPD patients displayed decreased lipoprotein and amino acids, including branched-chain amino acids (BCAAs), and increased glycerolphosphocholine in serum. Moreover, metabolic differences in urine were more significant than in serum. Decreased urinary 1-methylnicotinamide, creatinine and lactate have been discovered in COPD patients in comparison with healthy controls. Conversely, acetate, ketone bodies, carnosine, m-hydroxyphenylacetate, phenylacetyglycine, pyruvate and α-ketoglutarate exhibited enhanced expression levels in COPD patients relative to healthy subjects. Our results illustrate the potential application of NMR-based metabonomics in early diagnosis and understanding the mechanisms of COPD. Public Library of Science 2013-06-06 /pmc/articles/PMC3675021/ /pubmed/23755267 http://dx.doi.org/10.1371/journal.pone.0065675 Text en © 2013 Wang 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
Wang, Lingling
Tang, Yufu
Liu, Shuo
Mao, Shitao
Ling, Yuan
Liu, Dan
He, Xiaoyu
Wang, Xiaoge
Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals
title Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals
title_full Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals
title_fullStr Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals
title_full_unstemmed Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals
title_short Metabonomic Profiling of Serum and Urine by (1)H NMR-Based Spectroscopy Discriminates Patients with Chronic Obstructive Pulmonary Disease and Healthy Individuals
title_sort metabonomic profiling of serum and urine by (1)h nmr-based spectroscopy discriminates patients with chronic obstructive pulmonary disease and healthy individuals
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3675021/
https://www.ncbi.nlm.nih.gov/pubmed/23755267
http://dx.doi.org/10.1371/journal.pone.0065675
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