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First published online June 15, 2007, 10.2967/jnumed.107.040436
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Journal of Nuclear Medicine Vol. 48 No. 7 1053-1059
© 2007 by Society of Nuclear Medicine

doi: 10.2967/jnumed.107.040436

Clinical Investigation

Noninvasive Assessment of Crohn's Disease Intestinal Lesions with 18F-FDG PET/CT

Edouard Louis1, Geoffrey Ancion2, Arnaud Colard1, Veronique Spote3, Jacques Belaiche1 and Roland Hustinx2

1 Department of Gastroenterology, CHU of Liège, University of Liège, Liège, Belgium; 2 Department of Nuclear Medicine, CHU of Liège, University of Liège, Liège, Belgium; and 3 Department of Medical Imaging, CHU of Liège, University of Liège, Liège, Belgium

Correspondence: For correspondence or reprints contact: Edouard Louis, Service of Gastroenterology, CHU de Liège, 4000 Liège, Belgium. E-mail: Edouard.louis{at}ulg.ac.be

Pilot studies have shown good sensitivity and specificity for 18F-FDG PET in detecting gastrointestinal lesions of Crohn's disease. The combination of 18F-FDG PET with CT may further improve the localization and characterization of lesions with increased 18F-FDG uptake. Our aim was to assess the use of 18F-FDG PET/CT in evaluating the activity and location of Crohn's disease along the gastrointestinal tract. Methods: After giving informed consent, 22 patients with Crohn's disease were prospectively studied. They underwent 18F-FDG PET/CT, followed by ileocolonoscopy within 1 wk (mean, 2 d). The Crohn's disease activity index (CDAI) was calculated, and serum C-reactive protein (CRP) and fecal calprotectin were measured before endoscopy. The Crohn's disease endoscopy index of severity (CDEIS) was calculated during endoscopy. The global CDEIS score and endoscopic subscores for various ileocolonic segments were used for analysis. Results: Globally, 95 intestinal and colonic segments in 22 patients were analyzed. 18F-FDG PET/CT detected 35 of 48 endoscopically affected segments (sensitivity for the detection of endoscopic lesions, 72.9%). The sensitivity of 18F-FDG PET/CT for the detection of severe endoscopic lesions (deep ulcers and strictures) was 100% (14/14). The global PET/CT score significantly correlated with CDEIS (r = 0.51; 95% confidence interval [CI], 0.09–0.77; P = 0.017), CDAI (r = 0.58; 95% CI, 0.17–0.80; P = 0.005), and CRP (r = 0.56; 95% CI, 0.19–0.81; P = 0.007). Conclusion: 18F-FDG PET/CT was globally well correlated to the clinical, endoscopic, and biologic activity of Crohn's disease. Above all, this technique had a good sensitivity for the detection of intestinal and colonic segments with moderate to severe mucosal lesions. The potential impact of this promising tool on the global management of patients with Crohn's disease should be further evaluated in prospective studies.

Key Words: Crohn's disease • positron emission tomography • Crohn's disease endoscopic index of severity • CT scanner • Crohn's disease activity index

COPYRIGHT © 2007 by the Society of Nuclear Medicine, Inc.


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