Proton pump inhibitor therapy did not increase the prevalence of small-bowel injury: A propensity-matched analysis
Previous studies have reported that the suppression of acid secretion by using proton pump inhibitors (PPIs) results in dysbiosis of the small-bowel microbiota, leading to exacerbated small-bowel injuries, including erosions and ulcers. This study was designed to assess the association between PPI t...
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Published in | PloS one Vol. 12; no. 8; p. e0182586 |
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Main Authors | , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
Public Library of Science
03.08.2017
Public Library of Science (PLoS) |
Subjects | |
Online Access | Get full text |
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Summary: | Previous studies have reported that the suppression of acid secretion by using proton pump inhibitors (PPIs) results in dysbiosis of the small-bowel microbiota, leading to exacerbated small-bowel injuries, including erosions and ulcers. This study was designed to assess the association between PPI therapy and small-bowel lesions after adjustment for the differences in baseline characteristics between users and non-users of PPIs.
We retrospectively studied patients suspected to be suffering from small-bowel diseases, who underwent capsule endoscopy between 2010 and 2013. We used propensity matching to adjust for the differences in baseline characteristics between users and non-users of PPIs. The outcomes included the prevalence of small-bowel lesions: erosion, ulcer, angioectasia, varices, and tumor.
We selected 327 patient pairs for analysis after propensity matching, and found no significant differences in the prevalence of small-bowel injuries, including erosions and ulcers, between users and non-users of PPIs. Two subgroup analyses of the effect of the type of PPI and the effect of PPI therapy in users and non-users of nonsteroidal anti-inflammatory drugs indicated no significant differences in the prevalence of small-bowel injuries in these two groups.
PPI therapy did not increase the prevalence of small-bowel injury, regardless of the type of PPI used and the use of nonsteroidal anti-inflammatory drugs. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Competing Interests: Dr Mitsuhiro Fujishiro has received a lecture honorarium from Takeda Pharmaceutical Company Limited, Eisai Co., Ltd., Zeria Pharmaceutical Co., Ltd., and Nihon Parametric Technology, and a collaborative fund from HOYA-Pentax Company as a chief investigator of The University of Tokyo. Dr Atsushi Nakajima has received grant support from Ajinomoto Co. Inc., Astellas Pharma Inc., Takeda Pharmaceutical Company Limited, Mylan N.V., Otsuka Pharmaceutical Co., Ltd., Biofermin Seiyaku Co., Ltd., and Taisho Pharmaceutical Co., Ltd. Dr Naoki Ohmiya has received grant support from Ajinomoto Co. Inc., Japan Immunoresearch Laboratories Company Limited, Mitsubishi Tanabe Pharma Corporation, Medical Corporation Fukuyukai, and Eisai Co., Ltd. Dr. Takayuki Matsumoto has received grant support or speaker fees from EA Pharma Co., Ltd., Mitsubishi Tanabe Pharma Corporation, Japan Immunoresearch Laboratories Company Limited, Otsuka Pharmaceutical Co., Ltd., Daiichi Sankyo Company, Limited, Kyorin Pharmaceutical Co., Ltd., Kyowa Hakko Kirin Co., Ltd., and Jansen Pharmaceutical K.K. Dr Shinji Tanaka has received grant support or speaker fees from AstraZeneca K.K., Otsuka Pharmaceutical Co., Ltd., Daiichi Sankyo Company Limited, Eisai Co., Mitsubishi Tanabe Pharma Corporation, Zeria Pharmaceutical Co., Ltd., and Asahi Kasei Medical Co., Ltd.. Dr Choitsu Sakamoto has received speaker fees from Pfizer Japan Inc., Astellas Pharma Inc., and AstraZeneca K.K. The other authors declare no conflict of interest. This does not alter our adherence to PLOS ONE policies on sharing data and materials. |
ISSN: | 1932-6203 1932-6203 |
DOI: | 10.1371/journal.pone.0182586 |