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Diagnosis of inflammatory bowel disease (IBD) requires complex and invasive investigations and places a heavy burden, both
on healthcare resources, because of the cost, and on the individual, in times of disease-related disability and poor quality of
life. Recently, there has been increasing interest in non-invasive biomarkers to diagnose and monitor the disease activity. Since the
introduction of biological therapies, an increasing number of studies have focused on the utilization of non-invasive biomarkers of
inflammation. Among the more extensively investigated are standard serum markers such CRP, and faecal biomarkers, such as faecal
calprotectin (FC) and lactoferrin (FL). In general, although there are some limitations as these markers are also raised in systemic
infection / inflammation, colorectal cancer, NSAID-induced bowel inflammation and polyps. The development of sophisticated
analytical techniques has enabled the study and interpretation of changes in the faecal volatile organic metabolites (VOMs) and its
correlation with the pathophysiological mechanisms in the gut. VOMs are the chemicals that are the products and intermediates of
metabolism and may be altered in different bowel diseases. Changes in faecal VOMs should reflect GI disorders and could potentially
provide diagnostic information about these conditions. Multiple studies reported the differences in VOM profiles of healthy controls
vs. patients with active and inactive IBD. VOM profiles have been used to segregate patients by disease activity and, in the case of
colitis, the type of disease. The correlation of VOMs with microbiota is interesting and supports the hypothesis of gut microbial
dysbiosis in the etiology of IBD. This provides an important platform to explore the role of dysbiosis in IBD pathogenesis and
development of novel therapeutic targets. In future, further understanding of faecal VOMs may lead to the development of a rapid
and simple point of care diagnosis and monitoring of IBD.