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Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer
BACKGROUND: Colorectal cancer remains a leading cause of mortality and morbidity. The UK Bowel Cancer Screening Programme (BCSP) has demonstrated that detection of colorectal cancer at an earlier stage and identification of advanced pre‐malignant adenomas reduces mortality and morbidity. AIM: To ass...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593415/ https://www.ncbi.nlm.nih.gov/pubmed/30828825 http://dx.doi.org/10.1111/apt.15140 |
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author | Bond, Ashley Greenwood, Rosemary Lewis, Stephen Corfe, Bernard Sarkar, Sanchoy O'Toole, Paul Rooney, Paul Burkitt, Michael Hold, Georgina Probert, Chris |
author_facet | Bond, Ashley Greenwood, Rosemary Lewis, Stephen Corfe, Bernard Sarkar, Sanchoy O'Toole, Paul Rooney, Paul Burkitt, Michael Hold, Georgina Probert, Chris |
author_sort | Bond, Ashley |
collection | PubMed |
description | BACKGROUND: Colorectal cancer remains a leading cause of mortality and morbidity. The UK Bowel Cancer Screening Programme (BCSP) has demonstrated that detection of colorectal cancer at an earlier stage and identification of advanced pre‐malignant adenomas reduces mortality and morbidity. AIM: To assess the utility of volatile organic compounds as a biomarker for colorectal neoplasia. METHODS: Faeces were collected from symptomatic patients and people participating in the UK BCSP, prior to colonoscopy. Headspace extraction followed by gas chromatography mass spectrometry was performed on faeces to identify volatile organic compounds. Logistic regression modelling and 10‐fold cross‐validation were used to test potential biomarkers. RESULTS: One hundred and thirty‐seven participants were included (mean age 64 years [range 22‐85], 54% were male): 60 had no neoplasia, 56 had adenomatous polyp(s) and 21 had adenocarcinoma. Propan‐2‐ol was significantly more abundant in the cancer samples (P < 0.0001, q = 0.004) with an area under ROC (AUROC) curve of 0.76. When combined with 3‐methylbutanoic acid the AUROC curve was 0.82, sensitivity 87.9% (95% CI 0.87‐0.99) and specificity 84.6% (95% CI 0.65‐1.0). Logistic regression analysis using the presence/absence of specific volatile organic compounds, identified a three volatile organic compound panel (propan‐2‐ol, hexan‐2‐one and ethyl 3‐methyl‐ butanoate) to have an AUROC of 0.73, with a person six times more likely to have cancer if all three volatile organic compounds were present (P < 0.0001). CONCLUSIONS: Volatile organic compound analysis may have a superior diagnostic ability for the identification of colorectal adenocarcinoma, when compared to other faecal biomarkers, including those currently employed in UK. Clinical trial details: National Research Ethics Service Committee South West ‐ Central Bristol (REC reference 14/SW/1162) with R&D approval from University of Liverpool and Broadgreen University Hospital Trust (UoL 001098). |
format | Online Article Text |
id | pubmed-6593415 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65934152019-07-10 Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer Bond, Ashley Greenwood, Rosemary Lewis, Stephen Corfe, Bernard Sarkar, Sanchoy O'Toole, Paul Rooney, Paul Burkitt, Michael Hold, Georgina Probert, Chris Aliment Pharmacol Ther Faecal Volatile Compounds as a Biomarker for Colorectal Neoplasia BACKGROUND: Colorectal cancer remains a leading cause of mortality and morbidity. The UK Bowel Cancer Screening Programme (BCSP) has demonstrated that detection of colorectal cancer at an earlier stage and identification of advanced pre‐malignant adenomas reduces mortality and morbidity. AIM: To assess the utility of volatile organic compounds as a biomarker for colorectal neoplasia. METHODS: Faeces were collected from symptomatic patients and people participating in the UK BCSP, prior to colonoscopy. Headspace extraction followed by gas chromatography mass spectrometry was performed on faeces to identify volatile organic compounds. Logistic regression modelling and 10‐fold cross‐validation were used to test potential biomarkers. RESULTS: One hundred and thirty‐seven participants were included (mean age 64 years [range 22‐85], 54% were male): 60 had no neoplasia, 56 had adenomatous polyp(s) and 21 had adenocarcinoma. Propan‐2‐ol was significantly more abundant in the cancer samples (P < 0.0001, q = 0.004) with an area under ROC (AUROC) curve of 0.76. When combined with 3‐methylbutanoic acid the AUROC curve was 0.82, sensitivity 87.9% (95% CI 0.87‐0.99) and specificity 84.6% (95% CI 0.65‐1.0). Logistic regression analysis using the presence/absence of specific volatile organic compounds, identified a three volatile organic compound panel (propan‐2‐ol, hexan‐2‐one and ethyl 3‐methyl‐ butanoate) to have an AUROC of 0.73, with a person six times more likely to have cancer if all three volatile organic compounds were present (P < 0.0001). CONCLUSIONS: Volatile organic compound analysis may have a superior diagnostic ability for the identification of colorectal adenocarcinoma, when compared to other faecal biomarkers, including those currently employed in UK. Clinical trial details: National Research Ethics Service Committee South West ‐ Central Bristol (REC reference 14/SW/1162) with R&D approval from University of Liverpool and Broadgreen University Hospital Trust (UoL 001098). John Wiley and Sons Inc. 2019-03-03 2019-04 /pmc/articles/PMC6593415/ /pubmed/30828825 http://dx.doi.org/10.1111/apt.15140 Text en © 2019 The Authors. Alimentary Pharmacology & Therapeutics Published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Faecal Volatile Compounds as a Biomarker for Colorectal Neoplasia Bond, Ashley Greenwood, Rosemary Lewis, Stephen Corfe, Bernard Sarkar, Sanchoy O'Toole, Paul Rooney, Paul Burkitt, Michael Hold, Georgina Probert, Chris Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer |
title | Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer |
title_full | Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer |
title_fullStr | Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer |
title_full_unstemmed | Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer |
title_short | Volatile organic compounds emitted from faeces as a biomarker for colorectal cancer |
title_sort | volatile organic compounds emitted from faeces as a biomarker for colorectal cancer |
topic | Faecal Volatile Compounds as a Biomarker for Colorectal Neoplasia |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6593415/ https://www.ncbi.nlm.nih.gov/pubmed/30828825 http://dx.doi.org/10.1111/apt.15140 |
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