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Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study
Aspirin (ASA) exerts an anti-tumor effect via the COX pathway. Clinical studies on the chemopreventive effects of ASA on uterine cancer (UC) remain inconsistent. We used population-based retrospective cohort study to evaluate the UC in ASA users in Taiwanese women. From insurance claims data, we ide...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402752/ https://www.ncbi.nlm.nih.gov/pubmed/32756162 http://dx.doi.org/10.1097/MD.0000000000021446 |
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author | Li, Pei-Chen Sung, Fung-Chang Yang, Yu-Cih Chen, Weishan Wang, Jen-Hung Lin, Shinn-Zong Ding, Dah-Ching |
author_facet | Li, Pei-Chen Sung, Fung-Chang Yang, Yu-Cih Chen, Weishan Wang, Jen-Hung Lin, Shinn-Zong Ding, Dah-Ching |
author_sort | Li, Pei-Chen |
collection | PubMed |
description | Aspirin (ASA) exerts an anti-tumor effect via the COX pathway. Clinical studies on the chemopreventive effects of ASA on uterine cancer (UC) remain inconsistent. We used population-based retrospective cohort study to evaluate the UC in ASA users in Taiwanese women. From insurance claims data, we identified 23,342 women received ASA treatment between 2000 and 2010 and a comparison group of same sample size randomly selected from the same database matched by the propensity score. The incidence of UC in the ASA cohort was 10% of that in the comparison group (0.28 vs 2.73 per 10,000 person-years). The Poisson regression analysis estimated adjusted incidence rate ratio (IRR) was 0.10 (95% confidence interval (CI) = 0.09–0.11) for ASA users relatives to comparisons after controlling for covariates. The UC incidence in ASA users decreased with age, from 0.61 per 10,000 person-years in the 20 to 39 years old (adjusted IRR = 0.21, 95% CI = 0.15–0.29) to 0.21 per 10,000 person-years in the 65 to 80 years old (adjusted IRR = 0.15, 95% CI = 0.12–0.16). The incidence was higher in longer term users. Hormone therapy of estradiol was associated with the increase of UC risk in both cohorts, but less in ASA users than comparisons (1.34 vs 4.75 per 10,000 person-years). This study suggests that ASA use was associated with a decreased risk of UC. Further prospective randomized clinical trials are warranted to confirm the association. |
format | Online Article Text |
id | pubmed-7402752 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-74027522020-08-05 Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study Li, Pei-Chen Sung, Fung-Chang Yang, Yu-Cih Chen, Weishan Wang, Jen-Hung Lin, Shinn-Zong Ding, Dah-Ching Medicine (Baltimore) 5600 Aspirin (ASA) exerts an anti-tumor effect via the COX pathway. Clinical studies on the chemopreventive effects of ASA on uterine cancer (UC) remain inconsistent. We used population-based retrospective cohort study to evaluate the UC in ASA users in Taiwanese women. From insurance claims data, we identified 23,342 women received ASA treatment between 2000 and 2010 and a comparison group of same sample size randomly selected from the same database matched by the propensity score. The incidence of UC in the ASA cohort was 10% of that in the comparison group (0.28 vs 2.73 per 10,000 person-years). The Poisson regression analysis estimated adjusted incidence rate ratio (IRR) was 0.10 (95% confidence interval (CI) = 0.09–0.11) for ASA users relatives to comparisons after controlling for covariates. The UC incidence in ASA users decreased with age, from 0.61 per 10,000 person-years in the 20 to 39 years old (adjusted IRR = 0.21, 95% CI = 0.15–0.29) to 0.21 per 10,000 person-years in the 65 to 80 years old (adjusted IRR = 0.15, 95% CI = 0.12–0.16). The incidence was higher in longer term users. Hormone therapy of estradiol was associated with the increase of UC risk in both cohorts, but less in ASA users than comparisons (1.34 vs 4.75 per 10,000 person-years). This study suggests that ASA use was associated with a decreased risk of UC. Further prospective randomized clinical trials are warranted to confirm the association. Wolters Kluwer Health 2020-07-31 /pmc/articles/PMC7402752/ /pubmed/32756162 http://dx.doi.org/10.1097/MD.0000000000021446 Text en Copyright © 2020 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc/4.0 |
spellingShingle | 5600 Li, Pei-Chen Sung, Fung-Chang Yang, Yu-Cih Chen, Weishan Wang, Jen-Hung Lin, Shinn-Zong Ding, Dah-Ching Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study |
title | Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study |
title_full | Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study |
title_fullStr | Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study |
title_full_unstemmed | Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study |
title_short | Aspirin associated with a decreased incidence of uterine cancer: A retrospective population-based cohort study |
title_sort | aspirin associated with a decreased incidence of uterine cancer: a retrospective population-based cohort study |
topic | 5600 |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7402752/ https://www.ncbi.nlm.nih.gov/pubmed/32756162 http://dx.doi.org/10.1097/MD.0000000000021446 |
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