Cargando…
Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion
Pleural effusion is a common clinical manifestation with various causes. Current diagnostic and therapeutic methods have exhibited numerous limitations. By involving the analysis of dynamic changes in low molecular weight catabolites, metabolomics has been widely applied in various types of disease...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562006/ https://www.ncbi.nlm.nih.gov/pubmed/28627685 http://dx.doi.org/10.3892/mmr.2017.6758 |
_version_ | 1783257904648814592 |
---|---|
author | Wang, Cheng Peng, Jingjin Kuang, Yanling Zhang, Jiaqiang Dai, Luming |
author_facet | Wang, Cheng Peng, Jingjin Kuang, Yanling Zhang, Jiaqiang Dai, Luming |
author_sort | Wang, Cheng |
collection | PubMed |
description | Pleural effusion is a common clinical manifestation with various causes. Current diagnostic and therapeutic methods have exhibited numerous limitations. By involving the analysis of dynamic changes in low molecular weight catabolites, metabolomics has been widely applied in various types of disease and have provided platforms to distinguish many novel biomarkers. However, to the best of our knowledge, there are few studies regarding the metabolic profiling for pleural effusion. In the current study, 58 pleural effusion samples were collected, among which 20 were malignant pleural effusions, 20 were tuberculous pleural effusions and 18 were transudative pleural effusions. The small molecule metabolite spectrums were obtained by adopting (1)H nuclear magnetic resonance technology, and pattern-recognition multi-variable statistical analysis was used to screen out different metabolites. One-way analysis of variance, and Student-Newman-Keuls and the Kruskal-Wallis test were adopted for statistical analysis. Over 400 metabolites were identified in the untargeted metabolomic analysis and 26 metabolites were identified as significantly different among tuberculous, malignant and transudative pleural effusions. These metabolites were predominantly involved in the metabolic pathways of amino acids metabolism, glycometabolism and lipid metabolism. Statistical analysis revealed that eight metabolites contributed to the distinction between the three groups: Tuberculous, malignant and transudative pleural effusion. In the current study, the feasibility of identifying small molecule biochemical profiles in different types of pleural effusion were investigated reveal novel biological insights into the underlying mechanisms. The results provide specific insights into the biology of tubercular, malignant and transudative pleural effusion and may offer novel strategies for the diagnosis and therapy of associated diseases, including tuberculosis, advanced lung cancer and congestive heart failure. |
format | Online Article Text |
id | pubmed-5562006 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-55620062017-10-23 Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion Wang, Cheng Peng, Jingjin Kuang, Yanling Zhang, Jiaqiang Dai, Luming Mol Med Rep Articles Pleural effusion is a common clinical manifestation with various causes. Current diagnostic and therapeutic methods have exhibited numerous limitations. By involving the analysis of dynamic changes in low molecular weight catabolites, metabolomics has been widely applied in various types of disease and have provided platforms to distinguish many novel biomarkers. However, to the best of our knowledge, there are few studies regarding the metabolic profiling for pleural effusion. In the current study, 58 pleural effusion samples were collected, among which 20 were malignant pleural effusions, 20 were tuberculous pleural effusions and 18 were transudative pleural effusions. The small molecule metabolite spectrums were obtained by adopting (1)H nuclear magnetic resonance technology, and pattern-recognition multi-variable statistical analysis was used to screen out different metabolites. One-way analysis of variance, and Student-Newman-Keuls and the Kruskal-Wallis test were adopted for statistical analysis. Over 400 metabolites were identified in the untargeted metabolomic analysis and 26 metabolites were identified as significantly different among tuberculous, malignant and transudative pleural effusions. These metabolites were predominantly involved in the metabolic pathways of amino acids metabolism, glycometabolism and lipid metabolism. Statistical analysis revealed that eight metabolites contributed to the distinction between the three groups: Tuberculous, malignant and transudative pleural effusion. In the current study, the feasibility of identifying small molecule biochemical profiles in different types of pleural effusion were investigated reveal novel biological insights into the underlying mechanisms. The results provide specific insights into the biology of tubercular, malignant and transudative pleural effusion and may offer novel strategies for the diagnosis and therapy of associated diseases, including tuberculosis, advanced lung cancer and congestive heart failure. D.A. Spandidos 2017-08 2017-06-12 /pmc/articles/PMC5562006/ /pubmed/28627685 http://dx.doi.org/10.3892/mmr.2017.6758 Text en Copyright: © Wang et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Wang, Cheng Peng, Jingjin Kuang, Yanling Zhang, Jiaqiang Dai, Luming Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion |
title | Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion |
title_full | Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion |
title_fullStr | Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion |
title_full_unstemmed | Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion |
title_short | Metabolomic analysis based on (1)H-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion |
title_sort | metabolomic analysis based on (1)h-nuclear magnetic resonance spectroscopy metabolic profiles in tuberculous, malignant and transudative pleural effusion |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5562006/ https://www.ncbi.nlm.nih.gov/pubmed/28627685 http://dx.doi.org/10.3892/mmr.2017.6758 |
work_keys_str_mv | AT wangcheng metabolomicanalysisbasedon1hnuclearmagneticresonancespectroscopymetabolicprofilesintuberculousmalignantandtransudativepleuraleffusion AT pengjingjin metabolomicanalysisbasedon1hnuclearmagneticresonancespectroscopymetabolicprofilesintuberculousmalignantandtransudativepleuraleffusion AT kuangyanling metabolomicanalysisbasedon1hnuclearmagneticresonancespectroscopymetabolicprofilesintuberculousmalignantandtransudativepleuraleffusion AT zhangjiaqiang metabolomicanalysisbasedon1hnuclearmagneticresonancespectroscopymetabolicprofilesintuberculousmalignantandtransudativepleuraleffusion AT dailuming metabolomicanalysisbasedon1hnuclearmagneticresonancespectroscopymetabolicprofilesintuberculousmalignantandtransudativepleuraleffusion |