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Measurement of Prostaglandin Metabolites is Useful in Diagnosis of Small Bowel Ulcerations

Abstract

Background: We recently reported on a hereditary enteropathy associated with a gene encoding a prostaglandin transporter and referred to as chronic enteropathy associated with gene (CEAS). Crohn's disease (CD) is a major differential diagnosis of CEAS, because these diseases share some clinical features. Therefore, there is a need to develop a convenient screening test to distinguish CEAS from CD.

Aim: To examine whether prostaglandin E major urinary metabolites (PGE-MUM) can serve as a biomarker to distinguish CEAS from CD.

Methods: This was a transactional study of 20 patients with CEAS and 98 patients with CD. CEAS was diagnosed by the confirmation of homozygous or compound heterozygous mutation of . We measured the concentration of PGE-MUM in spot urine by radioimmunoassay, and the concentration was compared between the two groups of patients. We also determined the optimal cut-off value of PGE-MUM to distinguish CEAS from CD by receiver operating characteristic (ROC) curve analysis.

Results: Twenty Japanese patients with CEAS and 98 patients with CD were enrolled. PGE-MUM concentration in patients with CEAS was significantly higher than that in patients with CD (median 102.7 27.9 μg/g × Cre, < 0.0001). One log unit increase in PGE-MUM contributed to 7.3 increase in the likelihood for the diagnosis of CEAS [95% confidence interval (CI) 3.2-16.7]. A logistic regression analysis revealed that the association was significant even after adjusting confounding factors (adjusted odds ratio 29.6, 95%CI 4.7-185.7). ROC curve analysis revealed the optimal PGE-MUM cut-off value for the distinction of CEAS from CD to be 48.9 μg/g × Cre with 95.0% sensitivity and 79.6% specificity.

Conclusion: PGE-MUM measurement is a convenient, non-invasive and useful test for the distinction of CEAS from CD.

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References
1.
Fujiwara M, Okayasu I, Oritsu M, Komatsu J, Yoshitsugu M, Katoh Y . Significant increase in prostaglandin E-main urinary metabolite by laxative administration: comparison with ulcerative colitis. Digestion. 2000; 61(3):201-6. DOI: 10.1159/000007758. View

2.
Iddan G, Meron G, Glukhovsky A, Swain P . Wireless capsule endoscopy. Nature. 2000; 405(6785):417. DOI: 10.1038/35013140. View

3.
Perlemuter G, Guillevin L, Legman P, WEISS L, Couturier D, Chaussade S . Cryptogenetic multifocal ulcerous stenosing enteritis: an atypical type of vasculitis or a disease mimicking vasculitis. Gut. 2001; 48(3):333-8. PMC: 1760126. DOI: 10.1136/gut.48.3.333. View

4.
Yamamoto H, Sekine Y, Sato Y, Higashizawa T, Miyata T, Iino S . Total enteroscopy with a nonsurgical steerable double-balloon method. Gastrointest Endosc. 2001; 53(2):216-20. DOI: 10.1067/mge.2001.112181. View

5.
Kunikata T, Tanaka A, Miyazawa T, Kato S, Takeuchi K . 16,16-Dimethyl prostaglandin E2 inhibits indomethacin-induced small intestinal lesions through EP3 and EP4 receptors. Dig Dis Sci. 2002; 47(4):894-904. DOI: 10.1023/a:1014725024519. View