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A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis
Early diagnosis of liver cirrhosis may prevent progression and development of complications. Liver biopsy is the current standard, but is invasive and associated with morbidity. We aimed to identify exhaled volatiles within a heterogeneous group of chronic liver disease (CLD) patients that discrimin...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731784/ https://www.ncbi.nlm.nih.gov/pubmed/26822454 http://dx.doi.org/10.1038/srep19903 |
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author | Pijls, Kirsten E. Smolinska, Agnieszka Jonkers, Daisy M. A. E. Dallinga, Jan W. Masclee, Ad A. M. Koek, Ger H. van Schooten, Frederik-Jan |
author_facet | Pijls, Kirsten E. Smolinska, Agnieszka Jonkers, Daisy M. A. E. Dallinga, Jan W. Masclee, Ad A. M. Koek, Ger H. van Schooten, Frederik-Jan |
author_sort | Pijls, Kirsten E. |
collection | PubMed |
description | Early diagnosis of liver cirrhosis may prevent progression and development of complications. Liver biopsy is the current standard, but is invasive and associated with morbidity. We aimed to identify exhaled volatiles within a heterogeneous group of chronic liver disease (CLD) patients that discriminates those with compensated cirrhosis (CIR) from those without cirrhosis, and compare this with serological markers. Breath samples were collected from 87 CLD and 34 CIR patients. Volatiles in exhaled air were measured by gas chromatography mass spectrometry. Discriminant Analysis was performed to identify the optimal panel of serological markers and VOCs for classifying our patients using a random training set of 27 CIR and 27 CLD patients. Two randomly selected independent internal validation sets and permutation test were used to validate the model. 5 serological markers were found to distinguish CIR and CLD patients with a sensitivity of 0.71 and specificity of 0.84. A set of 11 volatiles discriminated CIR from CLD patients with sensitivity of 0.83 and specificity of 0.87. Combining both did not further improve accuracy. A specific exhaled volatile profile can predict the presence of compensated cirrhosis among CLD patients with a higher accuracy than serological markers and can aid in reducing liver biopsies. |
format | Online Article Text |
id | pubmed-4731784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47317842016-02-04 A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis Pijls, Kirsten E. Smolinska, Agnieszka Jonkers, Daisy M. A. E. Dallinga, Jan W. Masclee, Ad A. M. Koek, Ger H. van Schooten, Frederik-Jan Sci Rep Article Early diagnosis of liver cirrhosis may prevent progression and development of complications. Liver biopsy is the current standard, but is invasive and associated with morbidity. We aimed to identify exhaled volatiles within a heterogeneous group of chronic liver disease (CLD) patients that discriminates those with compensated cirrhosis (CIR) from those without cirrhosis, and compare this with serological markers. Breath samples were collected from 87 CLD and 34 CIR patients. Volatiles in exhaled air were measured by gas chromatography mass spectrometry. Discriminant Analysis was performed to identify the optimal panel of serological markers and VOCs for classifying our patients using a random training set of 27 CIR and 27 CLD patients. Two randomly selected independent internal validation sets and permutation test were used to validate the model. 5 serological markers were found to distinguish CIR and CLD patients with a sensitivity of 0.71 and specificity of 0.84. A set of 11 volatiles discriminated CIR from CLD patients with sensitivity of 0.83 and specificity of 0.87. Combining both did not further improve accuracy. A specific exhaled volatile profile can predict the presence of compensated cirrhosis among CLD patients with a higher accuracy than serological markers and can aid in reducing liver biopsies. Nature Publishing Group 2016-01-29 /pmc/articles/PMC4731784/ /pubmed/26822454 http://dx.doi.org/10.1038/srep19903 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pijls, Kirsten E. Smolinska, Agnieszka Jonkers, Daisy M. A. E. Dallinga, Jan W. Masclee, Ad A. M. Koek, Ger H. van Schooten, Frederik-Jan A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis |
title | A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis |
title_full | A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis |
title_fullStr | A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis |
title_full_unstemmed | A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis |
title_short | A profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis |
title_sort | profile of volatile organic compounds in exhaled air as a potential non-invasive biomarker for liver cirrhosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4731784/ https://www.ncbi.nlm.nih.gov/pubmed/26822454 http://dx.doi.org/10.1038/srep19903 |
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