TY - JOUR
T1 - Faecal gas analysis by electronic nose as novel, non-invasive method for assessment of active and quiescent paediatric inflammatory bowel disease
T2 - Proof of principle study
AU - De Meij, Tim G.J.
AU - de Boer, Nanne K.H.
AU - Benninga, Marc A.
AU - Lentferink, Yvette E.
AU - de Groot, Evelien F.J.
AU - van der Velden, Mirjam E.
AU - van Bodegraven, Adriaan A.
AU - van der Schee, Marc P.
PY - 2014/7/8
Y1 - 2014/7/8
N2 - Background and aims: Inflammatory bowel disease (IBD) and its two phenotypes ulcerative colitis (UC) and Crohn's disease (CD) are essentially assessed by endoscopy, both in initial diagnostic work-up and during follow-up. This carries a high burden, especially on paediatric patients. Faecal volatile organic compounds (VOCs) are considered potential non-invasive biomarkers for intestinal diseases linked to gut microbiota alterations. We hypothesized that faecal VOC analysis by electronic nose allows discrimination of children with CD, UC and controls during active disease and remission. Methods: Faecal VOC patterns of children with newly diagnosed IBD and controls were studied by an electronic nose (Cyranose 320®), at baseline and upon achieving remission at 6-weeks of follow-up. Disease activity was assessed by global physician's assessment, substantiated by serum C-reactive protein and faecal calprotectin. Internally cross-validated receiver-operator-characteristic curves and corresponding sensitivity and specificity for detection of IBD were calculated. . Results: Faecal VOC profiles of patients with UC (26) and CD (29) differed from controls (28); in active disease (AUC. ±. 95% CI, p-value, sensitivity, specificity: 1.00. ±. 0.00; p. <. 0.001, 100%, 100%) and (0.85. ±. 0.05, p. <. 0.001, 86%, 67%) and in clinical remission (0.94. ±. 0.06, p. <. 0.001, 94%, 94%) and (0.94. ±. 0.06, p. <. 0.001, 94%, 94%), respectively. Furthermore, CD-patients differed from UC-patients during active disease (0.96. ±. 0.03; p. <. 0.001, 97%, 92%), and upon achieving clinical remission (0.81. ±. 0.08, p. =. 0.002, 88%, 72%). Conclusion: Faecal VOC analysis allowed discrimination of paediatric patients with IBD from controls, both during active disease and remission. It therefore has potential as non-invasive test, in both diagnostic work-up and assessment of disease activity in IBD.
AB - Background and aims: Inflammatory bowel disease (IBD) and its two phenotypes ulcerative colitis (UC) and Crohn's disease (CD) are essentially assessed by endoscopy, both in initial diagnostic work-up and during follow-up. This carries a high burden, especially on paediatric patients. Faecal volatile organic compounds (VOCs) are considered potential non-invasive biomarkers for intestinal diseases linked to gut microbiota alterations. We hypothesized that faecal VOC analysis by electronic nose allows discrimination of children with CD, UC and controls during active disease and remission. Methods: Faecal VOC patterns of children with newly diagnosed IBD and controls were studied by an electronic nose (Cyranose 320®), at baseline and upon achieving remission at 6-weeks of follow-up. Disease activity was assessed by global physician's assessment, substantiated by serum C-reactive protein and faecal calprotectin. Internally cross-validated receiver-operator-characteristic curves and corresponding sensitivity and specificity for detection of IBD were calculated. . Results: Faecal VOC profiles of patients with UC (26) and CD (29) differed from controls (28); in active disease (AUC. ±. 95% CI, p-value, sensitivity, specificity: 1.00. ±. 0.00; p. <. 0.001, 100%, 100%) and (0.85. ±. 0.05, p. <. 0.001, 86%, 67%) and in clinical remission (0.94. ±. 0.06, p. <. 0.001, 94%, 94%) and (0.94. ±. 0.06, p. <. 0.001, 94%, 94%), respectively. Furthermore, CD-patients differed from UC-patients during active disease (0.96. ±. 0.03; p. <. 0.001, 97%, 92%), and upon achieving clinical remission (0.81. ±. 0.08, p. =. 0.002, 88%, 72%). Conclusion: Faecal VOC analysis allowed discrimination of paediatric patients with IBD from controls, both during active disease and remission. It therefore has potential as non-invasive test, in both diagnostic work-up and assessment of disease activity in IBD.
KW - Biomarkers
KW - Electronic nose
KW - Faecal gas analysis
KW - Flatography
KW - Inflammatory bowel disease
KW - Volatile organic compounds
UR - http://www.scopus.com/inward/record.url?scp=84913558006&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.crohns.2014.09.004
DO - https://doi.org/10.1016/j.crohns.2014.09.004
M3 - Article
SN - 1873-9946
JO - Journal of Crohn's and Colitis
JF - Journal of Crohn's and Colitis
ER -