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Use of acetaminophen and risk of endometrial cancer: evidence from observational studies

Previous meta-analyses suggested that aspirin was associated with reduced risk of endometrial cancer. However, there has been no study comprehensively summarize the evidence of acetaminophen use and risk of endometrial cancer from observational studies. We systematically searched electronic database...

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Autores principales: Ding, Yuan-Yuan, Yao, Peng, Verma, Surya, Han, Zhen-Kai, Hong, Tao, Zhu, Yong-Qiang, Li, Hong-Xi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470998/
https://www.ncbi.nlm.nih.gov/pubmed/28410226
http://dx.doi.org/10.18632/oncotarget.16663
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author Ding, Yuan-Yuan
Yao, Peng
Verma, Surya
Han, Zhen-Kai
Hong, Tao
Zhu, Yong-Qiang
Li, Hong-Xi
author_facet Ding, Yuan-Yuan
Yao, Peng
Verma, Surya
Han, Zhen-Kai
Hong, Tao
Zhu, Yong-Qiang
Li, Hong-Xi
author_sort Ding, Yuan-Yuan
collection PubMed
description Previous meta-analyses suggested that aspirin was associated with reduced risk of endometrial cancer. However, there has been no study comprehensively summarize the evidence of acetaminophen use and risk of endometrial cancer from observational studies. We systematically searched electronic databases (PubMed, EMBASE, Web of Science, and Cochrane Library) for relevant cohort or case-control studies up to February 28, 2017. Two independent authors performed the eligibility evaluation and data extraction. All differences were resolved by discussion. A random-effects model was applied to estimate summary relative risks (RRs) with 95% CIs. All statistical tests were two-sided. Seven observational studies including four prospective cohort studies and three case-control studies with 3874 endometrial cancer cases were included for final analysis. Compared with never use acetaminophen, ever use this drug was not associated with risk of endometrial cancer (summarized RR = 1.02; 95% CI: 0.93−1.13, I(2) = 0%). Similar null association was also observed when compared the highest category of frequency/duration with never use acetaminophen (summarized RR = 0.88; 95% CI: 0.70−1.11, I(2) = 15.2%). Additionally, the finding was robust in the subgroup analyses stratified by study characteristics and adjustment for potential confounders and risk factors. There was no evidence of publication bias by a visual inspection of a funnel plot and formal statistical tests. In summary, the present meta-analysis reveals no association between acetaminophen use and risk of endometrial cancer. More large scale prospective cohort studies are warranted to confirm our findings and carry out the dose-response analysis of aforementioned association.
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spelling pubmed-54709982017-06-27 Use of acetaminophen and risk of endometrial cancer: evidence from observational studies Ding, Yuan-Yuan Yao, Peng Verma, Surya Han, Zhen-Kai Hong, Tao Zhu, Yong-Qiang Li, Hong-Xi Oncotarget Research Paper Previous meta-analyses suggested that aspirin was associated with reduced risk of endometrial cancer. However, there has been no study comprehensively summarize the evidence of acetaminophen use and risk of endometrial cancer from observational studies. We systematically searched electronic databases (PubMed, EMBASE, Web of Science, and Cochrane Library) for relevant cohort or case-control studies up to February 28, 2017. Two independent authors performed the eligibility evaluation and data extraction. All differences were resolved by discussion. A random-effects model was applied to estimate summary relative risks (RRs) with 95% CIs. All statistical tests were two-sided. Seven observational studies including four prospective cohort studies and three case-control studies with 3874 endometrial cancer cases were included for final analysis. Compared with never use acetaminophen, ever use this drug was not associated with risk of endometrial cancer (summarized RR = 1.02; 95% CI: 0.93−1.13, I(2) = 0%). Similar null association was also observed when compared the highest category of frequency/duration with never use acetaminophen (summarized RR = 0.88; 95% CI: 0.70−1.11, I(2) = 15.2%). Additionally, the finding was robust in the subgroup analyses stratified by study characteristics and adjustment for potential confounders and risk factors. There was no evidence of publication bias by a visual inspection of a funnel plot and formal statistical tests. In summary, the present meta-analysis reveals no association between acetaminophen use and risk of endometrial cancer. More large scale prospective cohort studies are warranted to confirm our findings and carry out the dose-response analysis of aforementioned association. Impact Journals LLC 2017-03-29 /pmc/articles/PMC5470998/ /pubmed/28410226 http://dx.doi.org/10.18632/oncotarget.16663 Text en Copyright: © 2017 Ding et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Ding, Yuan-Yuan
Yao, Peng
Verma, Surya
Han, Zhen-Kai
Hong, Tao
Zhu, Yong-Qiang
Li, Hong-Xi
Use of acetaminophen and risk of endometrial cancer: evidence from observational studies
title Use of acetaminophen and risk of endometrial cancer: evidence from observational studies
title_full Use of acetaminophen and risk of endometrial cancer: evidence from observational studies
title_fullStr Use of acetaminophen and risk of endometrial cancer: evidence from observational studies
title_full_unstemmed Use of acetaminophen and risk of endometrial cancer: evidence from observational studies
title_short Use of acetaminophen and risk of endometrial cancer: evidence from observational studies
title_sort use of acetaminophen and risk of endometrial cancer: evidence from observational studies
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470998/
https://www.ncbi.nlm.nih.gov/pubmed/28410226
http://dx.doi.org/10.18632/oncotarget.16663
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