Jeremy Tibble
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Featured researches published by Jeremy Tibble.
Gut | 2000
Jeremy Tibble; Kathy Teahon; Bjarni Thjodleifsson; Arne G. Roseth; G Sigthorsson; S. Bridger; R Foster; R Sherwood; Magne K. Fagerhol; Ingvar Bjarnason
BACKGROUND AND AIMS Assessing the presence and degree of intestinal inflammation objectively, simply, and reliably is a significant problem in gastroenterology. We assessed faecal excretion of calprotectin, a stable neutrophil specific marker, as an index of intestinal inflammation and its potential use as a screening test to discriminate between patients with Crohns disease and those with irritable bowel syndrome. METHODS The validity of faecal calprotectin as a marker of intestinal inflammation was assessed in 22 patients with Crohns disease (35 studies) by comparing faecal excretions and concentrations using four day faecal excretion of111indium white cells. A cross sectional study assessed the sensitivity of faecal calprotectin concentration for the detection of established Crohns disease (n=116). A prospective study assessed the value of faecal calprotectin in discriminating between patients with Crohns disease and irritable bowel syndrome in 220 patients referred to a gastroenterology clinic. RESULTS Four day faecal excretion of 111indium (median 8.7%; 95% confidence interval (CI) 7–17%; normal <1.0%) correlated significantly (p<0.0001) with daily (median ranged from 39 to 47 mg; normal <3 mg; r=0.76–0.82) and four day faecal calprotectin excretion (median 101 mg; 95% CI 45–168 mg; normal <11 mg; r=0.80) and single stool calprotectin concentrations (median 118 mg/l; 95% CI 36–175 mg/l; normal <10 mg/l; r=0.70) in patients with Crohns disease. The cross sectional study showed a sensitivity of 96% for calprotectin in discriminating between normal subjects (2 mg/l; 95% CI 2–3 mg/l) and those with Crohns disease (91 mg/l; 95% CI 59–105 mg/l). With a cut off point of 30 mg/l faecal calprotectin has 100% sensitivity and 97% specificity in discriminating between active Crohns disease and irritable bowel syndrome. CONCLUSION The calprotectin method may be a useful adjuvant for discriminating between patients with Crohns disease and irritable bowel syndrome.
Gut | 1999
Jeremy Tibble; G Sigthorsson; R Foster; David Scott; Magne K. Fagerhol; A Roseth; Ingvar Bjarnason
BACKGROUND The diagnosis of non-steroidal anti-inflammatory drug (NSAID) induced enteropathy is difficult, requiring enteroscopy or the use of four day faecal excretion of 111In labelled white cells. AIMS To assess faecal calprotectin (a non-degraded neutrophil cytosolic protein) as a method for diagnosing NSAID enteropathy. METHODS Single stool faecal calprotectin concentrations were compared with the four day faecal excretion of 111In labelled white cells in 47 patients taking NSAIDs. The prevalence and severity of NSAID enteropathy was assessed using this method in 312 patients (192 with rheumatoid arthritis, 65 with osteoarthritis, 55 with other conditions) taking 18 different NSAIDs. RESULTS The four day faecal excretion of 111In white cells correlated significantly with faecal calprotectin concentrations. In the group of 312 patients on NSAIDs faecal calprotectin concentrations were significantly higher than in controls, the prevalence of NSAID enteropathy being 44%. The prevalence and severity of NSAID enteropathy was independent of the particular type or dose of NSAID being taken or other patient variables. CONCLUSIONS Assay of faecal calprotectin provides a simple practical method for diagnosing NSAID enteropathy in man. Forty four per cent of patients receiving these drugs had NSAID induced enteropathy when assessed by this technique; 20% of these had comparable levels of inflammation to that previously reported in patients with inflammatory bowel disease.
Current Opinion in Gastroenterology | 2000
Simon Smale; Jeremy Tibble; Ingvar Bjarnason
The noninvasive assessment of small intestinal permeability in humans is now within the capability of any routine biochemistry laboratory. There remain however, many pitfalls for the unwary when performing these tests. Importantly, it has now been shown that normal intestinal permeability relates to geographical location rather than race. Recent studies show that it may be possible to simplify the procedure even further. The main recent focus of interest in measuring intestinal permeability relates to patients with AIDS and inflammatory bowel disease, the effects of nonsteroidal anti-inflammatory drugs on the small bowel, and the use of these tests in the pediatric population and critically ill. Some groups have now started to focus their attention on the possible systemic consequences of increased intestinal permeability, whereas others have shown that increased small bowel permeability results in small intestinal inflammation that may in turn be associated with blood and protein loss.
Alimentary Pharmacology & Therapeutics | 2001
Jeremy Tibble; G Sigthorsson; C Caldwell; R H Palmer; Ingvar Bjarnason
Failure of ulcer healing may be critically important to the development of serious gastrointestinal complications in patients on long‐term NSAIDs.
Gastroenterology | 2000
Jeremy Tibble; G Sigthorsson; S. Bridger; Magne K. Fagerhol; Ingvar Bjarnason
Gastroenterology | 2002
Jeremy Tibble; G Sigthorsson; R Foster; Ian Forgacs; Ingvar Bjarnason
Gut | 2001
Jeremy Tibble; G Sigthorsson; R Foster; R Sherwood; Magne K. Fagerhol; Ingvar Bjarnason
Best Practice & Research in Clinical Gastroenterology | 2001
Simon Smale; Jeremy Tibble; G Sigthorsson; Ingvar Bjarnason
Gastroenterology | 1998
Jeremy Tibble; R Foster; G Sigthorsson; D Scott; A Roseth; Ingvar Bjarnason
Endoscopy | 2000
Jeremy Tibble; Ian Forgacs; Ingvar Bjarnason; R Przemioslo