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Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population
Although statin use may affect the severity of chronic gastritis and gastric cancer, no data exists about the relationship between statin therapy and risk of peptic ulcer disease (PUD) in patients. We investigated the effect of statin use and the incidence of PUD from the Taiwan National Health Insu...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408271/ https://www.ncbi.nlm.nih.gov/pubmed/28503146 http://dx.doi.org/10.3389/fphar.2017.00210 |
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author | Lin, Chun-Jung Liao, Wei-Chih Chen, Yu-An Lin, Hwai-Jeng Feng, Chun-Lung Lin, Cheng-Li Lin, Ying-Ju Kao, Min-Chuan Huang, Mei-Zi Lai, Chih-Ho Kao, Chia-Hung |
author_facet | Lin, Chun-Jung Liao, Wei-Chih Chen, Yu-An Lin, Hwai-Jeng Feng, Chun-Lung Lin, Cheng-Li Lin, Ying-Ju Kao, Min-Chuan Huang, Mei-Zi Lai, Chih-Ho Kao, Chia-Hung |
author_sort | Lin, Chun-Jung |
collection | PubMed |
description | Although statin use may affect the severity of chronic gastritis and gastric cancer, no data exists about the relationship between statin therapy and risk of peptic ulcer disease (PUD) in patients. We investigated the effect of statin use and the incidence of PUD from the Taiwan National Health Insurance Research Database (NHIRD). A total of 35,194 patients records for medical claims were enrolled. We performed a population-based case-control analysis to compare the incidence of PUD in patients who were prescribed statins and that in patients who were not. In the univariate logistic analysis, we found that statin was not significant risk of PUD. However, a multivariate model indicates that satin use was significantly associated with a reduced risk of PUD (adjusted odds ratio [aOR] = 0.87, 95% CI = 0.82–0.93, P < 0.001). The cumulative defined daily dose (DDD) was analyzed. Patients who prescribed fluvastatin ≥280 DDD, atorvastatin ≥200 DDD, and pravastatin ≥130 DDD dramatically decreased risk for PUD (aOR = 0.58, 0.67, and 0.71; 95% CI = 0.46–0.74, 0.57–0.78, and 0.56–0.91, respectively). Our results showed that statin therapy reduced the risk of PUD and this was associated with the high cumulative DDD of prescribed statins. This study reveals that active use of statins to be associated with decreased risk for PUD. |
format | Online Article Text |
id | pubmed-5408271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-54082712017-05-12 Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population Lin, Chun-Jung Liao, Wei-Chih Chen, Yu-An Lin, Hwai-Jeng Feng, Chun-Lung Lin, Cheng-Li Lin, Ying-Ju Kao, Min-Chuan Huang, Mei-Zi Lai, Chih-Ho Kao, Chia-Hung Front Pharmacol Pharmacology Although statin use may affect the severity of chronic gastritis and gastric cancer, no data exists about the relationship between statin therapy and risk of peptic ulcer disease (PUD) in patients. We investigated the effect of statin use and the incidence of PUD from the Taiwan National Health Insurance Research Database (NHIRD). A total of 35,194 patients records for medical claims were enrolled. We performed a population-based case-control analysis to compare the incidence of PUD in patients who were prescribed statins and that in patients who were not. In the univariate logistic analysis, we found that statin was not significant risk of PUD. However, a multivariate model indicates that satin use was significantly associated with a reduced risk of PUD (adjusted odds ratio [aOR] = 0.87, 95% CI = 0.82–0.93, P < 0.001). The cumulative defined daily dose (DDD) was analyzed. Patients who prescribed fluvastatin ≥280 DDD, atorvastatin ≥200 DDD, and pravastatin ≥130 DDD dramatically decreased risk for PUD (aOR = 0.58, 0.67, and 0.71; 95% CI = 0.46–0.74, 0.57–0.78, and 0.56–0.91, respectively). Our results showed that statin therapy reduced the risk of PUD and this was associated with the high cumulative DDD of prescribed statins. This study reveals that active use of statins to be associated with decreased risk for PUD. Frontiers Media S.A. 2017-04-28 /pmc/articles/PMC5408271/ /pubmed/28503146 http://dx.doi.org/10.3389/fphar.2017.00210 Text en Copyright © 2017 Lin, Liao, Chen, Lin, Feng, Lin, Lin, Kao, Huang, Lai and Kao. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Lin, Chun-Jung Liao, Wei-Chih Chen, Yu-An Lin, Hwai-Jeng Feng, Chun-Lung Lin, Cheng-Li Lin, Ying-Ju Kao, Min-Chuan Huang, Mei-Zi Lai, Chih-Ho Kao, Chia-Hung Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population |
title | Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population |
title_full | Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population |
title_fullStr | Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population |
title_full_unstemmed | Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population |
title_short | Statin Therapy Is Associated with Reduced Risk of Peptic Ulcer Disease in the Taiwanese Population |
title_sort | statin therapy is associated with reduced risk of peptic ulcer disease in the taiwanese population |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5408271/ https://www.ncbi.nlm.nih.gov/pubmed/28503146 http://dx.doi.org/10.3389/fphar.2017.00210 |
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