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Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study

BACKGROUND: Low-dose aspirin and clopidogrel have demonstrated potential chemoprevention for colorectal cancer (CRC). Proton-pump inhibitors (PPI) are commonly prescribed with anticoagulation drugs, but the relationship between PPI and CRC is unclear. Moreover, evidence of CRC risk under direct oral...

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Autores principales: Ho, Pei-Huan, Hsiao, Hung-Chun, Chen, Chun-Wei, Chen, Hui-Ming, Lim, Siew-Na, Yeh, Chau-Ting, Kuo, Chia-Jung, Lin, Wey-Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082832/
https://www.ncbi.nlm.nih.gov/pubmed/35534834
http://dx.doi.org/10.1186/s12876-022-02314-w
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author Ho, Pei-Huan
Hsiao, Hung-Chun
Chen, Chun-Wei
Chen, Hui-Ming
Lim, Siew-Na
Yeh, Chau-Ting
Kuo, Chia-Jung
Lin, Wey-Ran
author_facet Ho, Pei-Huan
Hsiao, Hung-Chun
Chen, Chun-Wei
Chen, Hui-Ming
Lim, Siew-Na
Yeh, Chau-Ting
Kuo, Chia-Jung
Lin, Wey-Ran
author_sort Ho, Pei-Huan
collection PubMed
description BACKGROUND: Low-dose aspirin and clopidogrel have demonstrated potential chemoprevention for colorectal cancer (CRC). Proton-pump inhibitors (PPI) are commonly prescribed with anticoagulation drugs, but the relationship between PPI and CRC is unclear. Moreover, evidence of CRC risk under direct oral anticoagulant (DOAC) is limited. This study aimed to investigate the effects of anticoagulation drugs combined with or without PPI on the risks of CRC in Taiwan. METHODS: A retrospective case–control study of 1,024,227 cases based on the Chang Gung Research Database from 2010 to 2017 was performed. Clinical characteristics, indications, duration of anticoagulation and PPI use, and CRC occurrence data were collected. Logistic regression was employed to adjust for known confounders of CRC risk. RESULTS: Monotherapy of clopidogrel decreased the risk of CRC (AOR 0.70; 95% CI 0.60–0.83), while no protective effect was observed in aspirin alone or aspirin plus clopidogrel. DOAC did not affect CRC significantly. The risk of CRC increased in patients with PPI (AOR 1.38; 95% CI 1.28–1.49) and PPI plus DOAC (OR 3.91; 95% CI 1.49–10.27), while PPI plus aspirin decreased the risk of CRC (OR 0.48; 95% CI 0.32–0.73). PPI plus clopidogrel showed no significant effect on the CRC. CONCLUSION: This study suggests clopidogrel alone and PPI plus aspirin offer a preventative benefit against CRC in the Taiwanese population studied. The same effect was not observed in DOAC. Moreover, a significant increase in CRC was observed in patients on PPI monotherapy and PPI plus DOAC, suggesting a possible risk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02314-w.
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spelling pubmed-90828322022-05-10 Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study Ho, Pei-Huan Hsiao, Hung-Chun Chen, Chun-Wei Chen, Hui-Ming Lim, Siew-Na Yeh, Chau-Ting Kuo, Chia-Jung Lin, Wey-Ran BMC Gastroenterol Research BACKGROUND: Low-dose aspirin and clopidogrel have demonstrated potential chemoprevention for colorectal cancer (CRC). Proton-pump inhibitors (PPI) are commonly prescribed with anticoagulation drugs, but the relationship between PPI and CRC is unclear. Moreover, evidence of CRC risk under direct oral anticoagulant (DOAC) is limited. This study aimed to investigate the effects of anticoagulation drugs combined with or without PPI on the risks of CRC in Taiwan. METHODS: A retrospective case–control study of 1,024,227 cases based on the Chang Gung Research Database from 2010 to 2017 was performed. Clinical characteristics, indications, duration of anticoagulation and PPI use, and CRC occurrence data were collected. Logistic regression was employed to adjust for known confounders of CRC risk. RESULTS: Monotherapy of clopidogrel decreased the risk of CRC (AOR 0.70; 95% CI 0.60–0.83), while no protective effect was observed in aspirin alone or aspirin plus clopidogrel. DOAC did not affect CRC significantly. The risk of CRC increased in patients with PPI (AOR 1.38; 95% CI 1.28–1.49) and PPI plus DOAC (OR 3.91; 95% CI 1.49–10.27), while PPI plus aspirin decreased the risk of CRC (OR 0.48; 95% CI 0.32–0.73). PPI plus clopidogrel showed no significant effect on the CRC. CONCLUSION: This study suggests clopidogrel alone and PPI plus aspirin offer a preventative benefit against CRC in the Taiwanese population studied. The same effect was not observed in DOAC. Moreover, a significant increase in CRC was observed in patients on PPI monotherapy and PPI plus DOAC, suggesting a possible risk. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12876-022-02314-w. BioMed Central 2022-05-09 /pmc/articles/PMC9082832/ /pubmed/35534834 http://dx.doi.org/10.1186/s12876-022-02314-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Ho, Pei-Huan
Hsiao, Hung-Chun
Chen, Chun-Wei
Chen, Hui-Ming
Lim, Siew-Na
Yeh, Chau-Ting
Kuo, Chia-Jung
Lin, Wey-Ran
Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study
title Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study
title_full Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study
title_fullStr Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study
title_full_unstemmed Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study
title_short Anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study
title_sort anticoagulant drugs with or without proton pump inhibitor and colorectal cancer risk: a population-based, case–control study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9082832/
https://www.ncbi.nlm.nih.gov/pubmed/35534834
http://dx.doi.org/10.1186/s12876-022-02314-w
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