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The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries

OBJECTIVE: Aspirin usage is associated with increased risk of gastrointestinal bleeding. The present study explored the potential of teprenone, an antiulcerative, in preventing aspirin-related gastric mucosal injuries. METHODS: 280 patients with coronary diseases, naïve to aspirin medication, were a...

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Autores principales: Zhao, Jing, Fan, Yihong, Ye, Wu, Feng, Wen, Hu, Yue, Cai, Lijun, Lu, Bin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604287/
https://www.ncbi.nlm.nih.gov/pubmed/31316561
http://dx.doi.org/10.1155/2019/6532876
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author Zhao, Jing
Fan, Yihong
Ye, Wu
Feng, Wen
Hu, Yue
Cai, Lijun
Lu, Bin
author_facet Zhao, Jing
Fan, Yihong
Ye, Wu
Feng, Wen
Hu, Yue
Cai, Lijun
Lu, Bin
author_sort Zhao, Jing
collection PubMed
description OBJECTIVE: Aspirin usage is associated with increased risk of gastrointestinal bleeding. The present study explored the potential of teprenone, an antiulcerative, in preventing aspirin-related gastric mucosal injuries. METHODS: 280 patients with coronary diseases, naïve to aspirin medication, were admitted between 2011 and 2013 at the First Affiliated Hospital of Zhejiang Chinese Medical University and randomized into two groups (n = 140). The aspirin group received aspirin enteric-coated tablets 100 mg/day, while the aspirin+teprenone group received teprenone 50 mg 3 times/day along with aspirin. The patients were recorded for gastrointestinal symptoms and gastric mucosal injuries during a follow-up period of 12 months with 3-month intervals. RESULTS: During the 3-month follow-up, no significant difference was observed in the incidence rate of gastrointestinal symptoms between the two groups (P = 0.498). However, the incidence rate of gastrointestinal symptoms was significantly lower in the aspirin+teprenone group than in the aspirin group during the follow-ups at 6 months (P = 0.036) and 12 months (P = 0.036). The incidence rate of gastric mucosal injuries in the aspirin group was significantly increased at 12 months compared to that at 3 months (P = 0.016). The incidence rates at 12 months and cumulative for the entire follow-up period in the aspirin+teprenone group were both significantly lower than those of the aspirin group (P = 0.049 and P = 0.001, respectively). CONCLUSION: Long-term use of low-dose aspirin causes varying degrees of gastric mucosal damages and gastrointestinal symptoms; the severity will increase within a certain range with the extension of medication duration. Teprenone mitigates the gastrointestinal symptoms caused by low-dose aspirin, lowering both the incidence and severity of gastric mucosal injuries and exerting a positive protective effect.
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spelling pubmed-66042872019-07-17 The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries Zhao, Jing Fan, Yihong Ye, Wu Feng, Wen Hu, Yue Cai, Lijun Lu, Bin Gastroenterol Res Pract Research Article OBJECTIVE: Aspirin usage is associated with increased risk of gastrointestinal bleeding. The present study explored the potential of teprenone, an antiulcerative, in preventing aspirin-related gastric mucosal injuries. METHODS: 280 patients with coronary diseases, naïve to aspirin medication, were admitted between 2011 and 2013 at the First Affiliated Hospital of Zhejiang Chinese Medical University and randomized into two groups (n = 140). The aspirin group received aspirin enteric-coated tablets 100 mg/day, while the aspirin+teprenone group received teprenone 50 mg 3 times/day along with aspirin. The patients were recorded for gastrointestinal symptoms and gastric mucosal injuries during a follow-up period of 12 months with 3-month intervals. RESULTS: During the 3-month follow-up, no significant difference was observed in the incidence rate of gastrointestinal symptoms between the two groups (P = 0.498). However, the incidence rate of gastrointestinal symptoms was significantly lower in the aspirin+teprenone group than in the aspirin group during the follow-ups at 6 months (P = 0.036) and 12 months (P = 0.036). The incidence rate of gastric mucosal injuries in the aspirin group was significantly increased at 12 months compared to that at 3 months (P = 0.016). The incidence rates at 12 months and cumulative for the entire follow-up period in the aspirin+teprenone group were both significantly lower than those of the aspirin group (P = 0.049 and P = 0.001, respectively). CONCLUSION: Long-term use of low-dose aspirin causes varying degrees of gastric mucosal damages and gastrointestinal symptoms; the severity will increase within a certain range with the extension of medication duration. Teprenone mitigates the gastrointestinal symptoms caused by low-dose aspirin, lowering both the incidence and severity of gastric mucosal injuries and exerting a positive protective effect. Hindawi 2019-06-18 /pmc/articles/PMC6604287/ /pubmed/31316561 http://dx.doi.org/10.1155/2019/6532876 Text en Copyright © 2019 Jing Zhao et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zhao, Jing
Fan, Yihong
Ye, Wu
Feng, Wen
Hu, Yue
Cai, Lijun
Lu, Bin
The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries
title The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries
title_full The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries
title_fullStr The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries
title_full_unstemmed The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries
title_short The Protective Effect of Teprenone on Aspirin-Related Gastric Mucosal Injuries
title_sort protective effect of teprenone on aspirin-related gastric mucosal injuries
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6604287/
https://www.ncbi.nlm.nih.gov/pubmed/31316561
http://dx.doi.org/10.1155/2019/6532876
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