Detection of colorectal cancer (CRC) by urinary volatile organic compound analysis

Colorectal cancer (CRC) is a leading cause of cancer related death in Europe and the USA. There is no universally accepted effective non-invasive screening test for CRC. Guaiac based faecal occult blood (gFOB) testing has largely been superseded by Faecal Immunochemical testing (FIT), but sensitivit...

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Published inPloS one Vol. 9; no. 9; p. e108750
Main Authors Arasaradnam, Ramesh P, McFarlane, Michael J, Ryan-Fisher, Courtenay, Westenbrink, Erik, Hodges, Phoebe, Hodges, Paula, Thomas, Matthew G, Chambers, Samantha, O'Connell, Nicola, Bailey, Catherine, Harmston, Christopher, Nwokolo, Chuka U, Bardhan, Karna D, Covington, James A
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 30.09.2014
Public Library of Science (PLoS)
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Abstract Colorectal cancer (CRC) is a leading cause of cancer related death in Europe and the USA. There is no universally accepted effective non-invasive screening test for CRC. Guaiac based faecal occult blood (gFOB) testing has largely been superseded by Faecal Immunochemical testing (FIT), but sensitivity still remains poor. The uptake of population based FOBt testing in the UK is also low at around 50%. The detection of volatile organic compounds (VOCs) signature(s) for many cancer subtypes is receiving increasing interest using a variety of gas phase analytical instruments. One such example is FAIMS (Field Asymmetric Ion Mobility Spectrometer). FAIMS is able to identify Inflammatory Bowel disease (IBD) patients by analysing shifts in VOCs patterns in both urine and faeces. This study extends this concept to determine whether CRC patients can be identified through non-invasive analysis of urine, using FAIMS. 133 patients were recruited; 83 CRC patients and 50 healthy controls. Urine was collected at the time of CRC diagnosis and headspace analysis undertaken using a FAIMS instrument (Owlstone, Lonestar, UK). Data was processed using Fisher Discriminant Analysis (FDA) after feature extraction from the raw data. FAIMS analyses demonstrated that the VOC profiles of CRC patients were tightly clustered and could be distinguished from healthy controls. Sensitivity and specificity for CRC detection with FAIMS were 88% and 60% respectively. This study suggests that VOC signatures emanating from urine can be detected in patients with CRC using ion mobility spectroscopy technology (FAIMS) with potential as a novel screening tool.
AbstractList Colorectal cancer (CRC) is a leading cause of cancer related death in Europe and the USA. There is no universally accepted effective non-invasive screening test for CRC. Guaiac based faecal occult blood (gFOB) testing has largely been superseded by Faecal Immunochemical testing (FIT), but sensitivity still remains poor. The uptake of population based FOBt testing in the UK is also low at around 50%. The detection of volatile organic compounds (VOCs) signature(s) for many cancer subtypes is receiving increasing interest using a variety of gas phase analytical instruments. One such example is FAIMS (Field Asymmetric Ion Mobility Spectrometer). FAIMS is able to identify Inflammatory Bowel disease (IBD) patients by analysing shifts in VOCs patterns in both urine and faeces. This study extends this concept to determine whether CRC patients can be identified through non-invasive analysis of urine, using FAIMS. 133 patients were recruited; 83 CRC patients and 50 healthy controls. Urine was collected at the time of CRC diagnosis and headspace analysis undertaken using a FAIMS instrument (Owlstone, Lonestar, UK). Data was processed using Fisher Discriminant Analysis (FDA) after feature extraction from the raw data. FAIMS analyses demonstrated that the VOC profiles of CRC patients were tightly clustered and could be distinguished from healthy controls. Sensitivity and specificity for CRC detection with FAIMS were 88% and 60% respectively. This study suggests that VOC signatures emanating from urine can be detected in patients with CRC using ion mobility spectroscopy technology (FAIMS) with potential as a novel screening tool.
Audience Academic
Author Arasaradnam, Ramesh P
Hodges, Phoebe
Hodges, Paula
Covington, James A
Chambers, Samantha
Thomas, Matthew G
Westenbrink, Erik
Bailey, Catherine
Nwokolo, Chuka U
McFarlane, Michael J
O'Connell, Nicola
Ryan-Fisher, Courtenay
Bardhan, Karna D
Harmston, Christopher
AuthorAffiliation 2 School of Engineering, University of Warwick, Coventry, Warwickshire, United Kingdom
6 MOAC Doctoral Training Centre, University of Warwick, Coventry, Warwickshire, United Kingdom
3 Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
The University of Texas MD Anderson Cancer Center, United States of America
1 Clinical Sciences Research Institute, University of Warwick, Coventry, Warwickshire, United Kingdom
4 Department of Gastroenterology, Rotherham General Hospital, Rotherham, Yorkshire, United Kingdom
5 Department of Surgery, University Hospital Coventry and Warwickshire, Coventry, Warwickshire, United Kingdom
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  givenname: Ramesh P
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  organization: Clinical Sciences Research Institute, University of Warwick, Coventry, Warwickshire, United Kingdom; Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
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  surname: McFarlane
  fullname: McFarlane, Michael J
  organization: Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
– sequence: 3
  givenname: Courtenay
  surname: Ryan-Fisher
  fullname: Ryan-Fisher, Courtenay
  organization: Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
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  surname: Westenbrink
  fullname: Westenbrink, Erik
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  fullname: Hodges, Paula
  organization: Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
– sequence: 7
  givenname: Matthew G
  surname: Thomas
  fullname: Thomas, Matthew G
  organization: School of Engineering, University of Warwick, Coventry, Warwickshire, United Kingdom; MOAC Doctoral Training Centre, University of Warwick, Coventry, Warwickshire, United Kingdom
– sequence: 8
  givenname: Samantha
  surname: Chambers
  fullname: Chambers, Samantha
  organization: Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
– sequence: 9
  givenname: Nicola
  surname: O'Connell
  fullname: O'Connell, Nicola
  organization: Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
– sequence: 10
  givenname: Catherine
  surname: Bailey
  fullname: Bailey, Catherine
  organization: Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
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  givenname: Christopher
  surname: Harmston
  fullname: Harmston, Christopher
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  givenname: Chuka U
  surname: Nwokolo
  fullname: Nwokolo, Chuka U
  organization: Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom
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  givenname: Karna D
  surname: Bardhan
  fullname: Bardhan, Karna D
  organization: Clinical Sciences Research Institute, University of Warwick, Coventry, Warwickshire, United Kingdom; Department of Gastroenterology, Rotherham General Hospital, Rotherham, Yorkshire, United Kingdom
– sequence: 14
  givenname: James A
  surname: Covington
  fullname: Covington, James A
  organization: School of Engineering, University of Warwick, Coventry, Warwickshire, United Kingdom
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25268885$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright COPYRIGHT 2014 Public Library of Science
2014 Arasaradnam et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2014 Arasaradnam et al 2014 Arasaradnam et al
Copyright_xml – notice: COPYRIGHT 2014 Public Library of Science
– notice: 2014 Arasaradnam et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
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Competing Interests: The authors have declared that no competing interests exist.
Conceived and designed the experiments: RA CN KB JC. Performed the experiments: EW MT JC. Analyzed the data: RA MM EW MT JC. Contributed reagents/materials/analysis tools: RA EW MT JA. Wrote the paper: RA MM SC MT CH CN KB JC. Recruitment of patients: CRF PH NOC CB.
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Snippet Colorectal cancer (CRC) is a leading cause of cancer related death in Europe and the USA. There is no universally accepted effective non-invasive screening...
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StartPage e108750
SubjectTerms Adult
Aged
Analysis
Biomarkers
Biomarkers, Tumor - urine
Cancer
Cancer diagnosis
Chromatography
Cluster Analysis
Colorectal cancer
Colorectal carcinoma
Colorectal Neoplasms - diagnosis
Data processing
Discriminant Analysis
Disease
Engineering schools
Feature extraction
Female
Fermentation
Gas Chromatography-Mass Spectrometry
Gases
Gastroenterology
Gastrointestinal diseases
Headspace
Health aspects
Humans
Inflammatory bowel diseases
Intestine
Ion mobility spectroscopy
Ionic mobility
Male
Mass Spectrometry
Medical screening
Medicine and Health Sciences
Middle Aged
Mobility
Organic compounds
Patients
Pollution control
Prostate
Scientific imaging
Sensitivity
Sensitivity and Specificity
Spectroscopy
Tumors
Urine
VOCs
Volatile organic compounds
Volatile Organic Compounds - urine
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Title Detection of colorectal cancer (CRC) by urinary volatile organic compound analysis
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