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Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies

BACKGROUND: Epidemiological studies have clarified the potential associations between regular aspirin use and cancers. However, it remains controversial on whether aspirin use decreases the risk of cancers risks. Therefore, we conducted an updated meta-analysis to assess the associations between asp...

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Autores principales: Qiao, Yan, Yang, Tingting, Gan, Yong, Li, Wenzhen, Wang, Chao, Gong, Yanhong, Lu, Zuxun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851082/
https://www.ncbi.nlm.nih.gov/pubmed/29534696
http://dx.doi.org/10.1186/s12885-018-4156-5
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author Qiao, Yan
Yang, Tingting
Gan, Yong
Li, Wenzhen
Wang, Chao
Gong, Yanhong
Lu, Zuxun
author_facet Qiao, Yan
Yang, Tingting
Gan, Yong
Li, Wenzhen
Wang, Chao
Gong, Yanhong
Lu, Zuxun
author_sort Qiao, Yan
collection PubMed
description BACKGROUND: Epidemiological studies have clarified the potential associations between regular aspirin use and cancers. However, it remains controversial on whether aspirin use decreases the risk of cancers risks. Therefore, we conducted an updated meta-analysis to assess the associations between aspirin use and cancers. METHODS: The PubMed, Embase, and Web of Science databases were systematically searched up to March 2017 to identify relevant studies. Relative risks (RRs) with 95% confidence intervals (CIs) were used to assess the strength of associations. RESULTS: A total of 218 studies with 309 reports were eligible for this meta-analysis. Aspirin use was associated with a significant decrease in the risk of overall cancer (RR = 0.89, 95% CI: 0.87–0.91), and gastric (RR = 0.75, 95% CI: 0.65–0.86), esophageal (RR = 0.75, 95% CI: 0.62–0.89), colorectal (RR = 0.79, 95% CI: 0.74–0.85), pancreatic (RR = 0.80, 95% CI: 0.68–0.93), ovarian (RR = 0.89, 95% CI: 0.83–0.95), endometrial (RR = 0.92, 95% CI: 0.85–0.99), breast (RR = 0.92, 95% CI: 0.88–0.96), and prostate (RR = 0.94, 95% CI: 0.90–0.99) cancers, as well as small intestine neuroendocrine tumors (RR = 0.17, 95% CI: 0.05–0.58). CONCLUSIONS: These findings suggest that aspirin use is associated with a reduced risk of gastric, esophageal, colorectal, pancreatic, ovarian, endometrial, breast, and prostate cancers, and small intestine neuroendocrine tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4156-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-58510822018-03-21 Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies Qiao, Yan Yang, Tingting Gan, Yong Li, Wenzhen Wang, Chao Gong, Yanhong Lu, Zuxun BMC Cancer Research Article BACKGROUND: Epidemiological studies have clarified the potential associations between regular aspirin use and cancers. However, it remains controversial on whether aspirin use decreases the risk of cancers risks. Therefore, we conducted an updated meta-analysis to assess the associations between aspirin use and cancers. METHODS: The PubMed, Embase, and Web of Science databases were systematically searched up to March 2017 to identify relevant studies. Relative risks (RRs) with 95% confidence intervals (CIs) were used to assess the strength of associations. RESULTS: A total of 218 studies with 309 reports were eligible for this meta-analysis. Aspirin use was associated with a significant decrease in the risk of overall cancer (RR = 0.89, 95% CI: 0.87–0.91), and gastric (RR = 0.75, 95% CI: 0.65–0.86), esophageal (RR = 0.75, 95% CI: 0.62–0.89), colorectal (RR = 0.79, 95% CI: 0.74–0.85), pancreatic (RR = 0.80, 95% CI: 0.68–0.93), ovarian (RR = 0.89, 95% CI: 0.83–0.95), endometrial (RR = 0.92, 95% CI: 0.85–0.99), breast (RR = 0.92, 95% CI: 0.88–0.96), and prostate (RR = 0.94, 95% CI: 0.90–0.99) cancers, as well as small intestine neuroendocrine tumors (RR = 0.17, 95% CI: 0.05–0.58). CONCLUSIONS: These findings suggest that aspirin use is associated with a reduced risk of gastric, esophageal, colorectal, pancreatic, ovarian, endometrial, breast, and prostate cancers, and small intestine neuroendocrine tumors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12885-018-4156-5) contains supplementary material, which is available to authorized users. BioMed Central 2018-03-13 /pmc/articles/PMC5851082/ /pubmed/29534696 http://dx.doi.org/10.1186/s12885-018-4156-5 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Qiao, Yan
Yang, Tingting
Gan, Yong
Li, Wenzhen
Wang, Chao
Gong, Yanhong
Lu, Zuxun
Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
title Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
title_full Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
title_fullStr Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
title_full_unstemmed Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
title_short Associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
title_sort associations between aspirin use and the risk of cancers: a meta-analysis of observational studies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5851082/
https://www.ncbi.nlm.nih.gov/pubmed/29534696
http://dx.doi.org/10.1186/s12885-018-4156-5
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