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Histology of symptomatic gastroesophageal reflux disease: Is it predictive of response to proton pump inhibitors?

Authors :
Tadayuki Oshima
Junko Aida
Yoshikazu Kinoshita
Tomohiko Shimatani
Michio Hongo
Tsuneya Wada
Susumu Kurosawa
Takahisa Furuta
Junji Tanaka
Tsutomu Chiba
Kaiyo Takubo
Yusuke Watanabe
Takashi Joh
Yasuki Habu
Hiroto Miwa
Masanori Ito
Source :
Journal of Gastroenterology and Hepatology. 28:479-487
Publication Year :
2013
Publisher :
Wiley, 2013.

Abstract

Background and Aim To examine the differences in esophageal histopathology between non-erosive reflux disease (NERD) and reflux esophagitis (RE), and to investigate whether baseline esophageal histopathology can predict the therapeutic response to proton pump inhibitors (PPIs). Method The subjects comprised 94 patients with NERD (n = 71) or mild RE (n = 23). Tissue was biopsied from 5 cm above the squamo-columnar junction (SCJ), and the degree or presence of nine histopathological markers was assessed. The patients were treated with rabeprazole (RPZ) 10 mg once daily for 4 weeks. If complete heartburn relief was not achieved, RPZ was increased to 10 mg twice daily for another 2 weeks, and then to 20 mg twice daily for another 2 weeks if heartburn remained. Results Features of esophageal histopathology 5 cm above the SCJ differed between NERD and RE patients. The esophageal histopathology in patients unresponsive to RPZ was characterized by Protein Gene Product (PGP) 9.5 negativity in those with NERD, and intraepithelial bleeding in those with RE. In addition, the combination of dilated intercellular spaces (DIS) (+)/PGP 9.5 (−) was indicative of strong resistance to PPI therapy in NERD patients. Conclusion The therapeutic efficacy of PPI can be predicted from the features of biopsied esophageal tissue. Factors predictive of resistance to treatment with PPI are negativity for PGP 9.5 in NERD patients and intraepithelial bleeding in RE patients.

Details

ISSN :
08159319
Volume :
28
Database :
OpenAIRE
Journal :
Journal of Gastroenterology and Hepatology
Accession number :
edsair.doi...........2aea2ba39e4e1823ae5f7944ec83bcfa
Full Text :
https://doi.org/10.1111/j.1440-1746.2012.07266.x