Evidence map›Paper›PMID 25330367›Full record

ArticlePloS one2014

Differentiating coeliac disease from irritable bowel syndrome by urinary volatile organic compound analysis--a pilot study.

Ramesh P Arasaradnam, Eric Westenbrink, Michael J McFarlane, Ruth Harbord, Samantha Chambers, Nicola O'Connell, Catherine Bailey, Chuka U Nwokolo, Karna D Bardhan, Richard Savage and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 2 syntheses or guidelines pooled it, 84 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 1 country.

Ramesh P ArasaradnamClinical Sciences Research Institute, University of Warwick, Coventry, Warwickshire, United Kingdom; Department of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom.
Eric WestenbrinkSchool of Engineering, University of Warwick, Coventry, Warwickshire, United Kingdom.
Michael J McFarlaneDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom.
Ruth HarbordMOAC Doctoral Training Centre, University of Warwick, Coventry, Warwickshire, United Kingdom.
Samantha ChambersDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom.
Nicola O'ConnellDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom.
Catherine BaileyDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom.
Chuka U NwokoloDepartment of Gastroenterology, University Hospital Coventry & Warwickshire, Coventry, Warwickshire, United Kingdom.
Karna D BardhanRotherham General Hospital, Rotherham, Yorkshire, United Kingdom.
Richard SavageDepartment of Bioinformatics, University of Warwick, Coventry, Warwickshire, United Kingdom.
James A CovingtonSchool of Engineering, University of Warwick, Coventry, Warwickshire, United Kingdom.
University Hospital Coventry · GBUniversity of Warwick · GBRotherham General Hospital · GB

Funding

Medical Research Council G0902104
6 · The paper itself

Abstract

Coeliac disease (CD), a T-cell-mediated gluten sensitive enteropathy, affects ∼ 1% of the UK population and can present with wide ranging clinical features, often being mistaken for Irritable Bowel Syndrome (IBS). Heightened clinical awareness and serological screening identifies those with potential coeliac disease; the diagnosis is confirmed with duodenal biopsies, and symptom improvement with a gluten-free diet. Limitations to diagnosis are false negative serology and reluctance to undergo biopsy. The gut microbiome is altered in several gastrointestinal disorders, causing altered gut fermentation patterns recognisable by volatile organic compounds (VOC) analysis in urine, breath and faeces. We aimed to determine if CD alters the urinary VOC pattern, distinguishing it from IBS. 47 patients were recruited, 27 with established CD, on gluten free diets, and 20 with diarrhoea-predominant IBS (D-IBS). Collected urine was stored frozen in 10 ml aliquots. For assay, the specimens were heated to 40 ± 0.1°C and the headspace analysed by Field Asymmetric Ion Mobility Spectrometry (FAIMS). Machine learning algorithms were used for statistical evaluation. Samples were also analysed using Gas chromatography and mass spectroscopy (GC-MS). Sparse logistic regression showed that FAIMS distinguishes VOCs in CD vs D-IBS with ROC curve AUC of 0.91 (0.83-0.99), sensitivity and specificity of 85% respectively. GCMS showed a unique peak at 4'67 found only in CD, not D-IBS, which correlated with the compound 1,3,5,7 cyclooctatetraene. This study suggests that FAIMS offers a novel, non-invasive approach to identify those with possible CD, and distinguishes from D-IBS. It offers the potential for monitoring compliance with a gluten-free diet at home. The presence of cyclooctatetraene in CD specimens will need further validation.

Indexed as

AdultCeliac DiseaseDiagnosis, DifferentialFemaleGas Chromatography-Mass SpectrometryHumansIrritable Bowel SyndromeMaleMiddle AgedPilot ProjectsVolatile Organic CompoundsVolatile Organic Compounds

Identifiers

PMID25330367
PMCPMC4199520
OpenAlexW2022110523

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.