Capsule endoscopy in adult celiac disease: a potential role in equivocal cases of celiac disease?

There have been limited studies evaluating capsule endoscopy (CE) in equivocal celiac disease (CD). To determine the role CE may have in equivocal CD cases, compared with patients with biopsy-proven and serology-proven CD who have persisting symptoms. Prospective cohort study. University hospital. A total of 62 patients with equivocal CD and 69 patients with nonresponsive CD. CE. Diagnostic yield of CE in equivocal cases and accuracy of mucosal abnormality detection in patients with nonresponsive CD. Equivocal cases (n = 62) were divided into two subgroups: group A (antibody-negative villous atrophy, n = 32) and group B (Marsh 1-2 changes, n = 30). In group A, CE secured a diagnosis of CD or Crohn's disease in 28% (9/32), significantly higher than the diagnostic yield in group B (7%; P = .044). In patients with CD with persisting symptoms, significant CE findings were identified in 12% (8/69), including 2 cases of enteropathy-associated lymphoma, 4 type 1 refractory disease cases, 1 polypoidal mass histologically confirmed to be a fibroepithelial polyp, and 1 case of ulcerative jejunitis. This outcome was significantly lower than the diagnostic yield of CE in antibody-negative villous atrophy (P = .048). Single center. There have been no previous reports systematically evaluating equivocal CD by using CE. The diagnostic yield of CE in patients with antibody-negative villous atrophy is better than that of CE in patients with CD with persisting symptoms. We advocate the use of CE in equivocal cases, particularly in patients with antibody-negative villous atrophy. Copyright © 2013 American Society for Gastrointestinal Endoscopy. Published by Mosby, Inc. All rights reserved.

Citation

Matthew Kurien, Kate E Evans, Imran Aziz, Reena Sidhu, Kaye Drew, Thea L Rogers, Mark E McAlindon, David S Sanders. Capsule endoscopy in adult celiac disease: a potential role in equivocal cases of celiac disease? Gastrointestinal endoscopy. 2013 Feb;77(2):227-32

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PMID: 23200728

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