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Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis

BACKGROUND: Epidemiological evidence that glioma has a slight male predominance implies that factors associated with sex hormones may play a role in the development of glioma. The association between oral contraceptive (OC) use and glioma risk remains controversial. METHOD: In the Prostate, Lung, Co...

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Autores principales: Shao, Chuan, Tang, Hui, Wang, Xiaoya, He, Jiaquan, Wang, Pan, Wu, Nan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330220/
https://www.ncbi.nlm.nih.gov/pubmed/35910887
http://dx.doi.org/10.3389/fpubh.2022.878233
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author Shao, Chuan
Tang, Hui
Wang, Xiaoya
He, Jiaquan
Wang, Pan
Wu, Nan
author_facet Shao, Chuan
Tang, Hui
Wang, Xiaoya
He, Jiaquan
Wang, Pan
Wu, Nan
author_sort Shao, Chuan
collection PubMed
description BACKGROUND: Epidemiological evidence that glioma has a slight male predominance implies that factors associated with sex hormones may play a role in the development of glioma. The association between oral contraceptive (OC) use and glioma risk remains controversial. METHOD: In the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial of 70,516 women in the USA, Cox proportional hazards regression analyses were adopted to calculate the crude and adjusted hazard ratios (HRs) and 95% confidence intervals (CIs). Additionally, a meta-analysis combining the PLCO findings with those of other prospective cohorts was performed. RESULTS: During a mean follow-up of ~11.7 years, 110 of 70,516 women aged 50–78 years at baseline were diagnosed with glioma in PLCO studies. Compared with never users, an inverse association of borderline significance was found for OC users (HR 0.67, 95% CI 0.44–1.04, P = 0.074). Analyses assessing glioma risk according to the duration of OC use yielded no significant association. When PLCO was combined with four other prospective studies, there was an inverse association between OC use and glioma risk (HR 0.85, 95% CI 0.75–0.97, I(2) = 0.0%). Further dose-response analysis showed a nonlinear, inverse relationship between OC use and glioma risk (P < 0.001). CONCLUSIONS: This study provided some evidence of a nonlinear, inverse association between OC use and glioma risk. Future larger studies are warranted to validate this finding.
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spelling pubmed-93302202022-07-29 Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis Shao, Chuan Tang, Hui Wang, Xiaoya He, Jiaquan Wang, Pan Wu, Nan Front Public Health Public Health BACKGROUND: Epidemiological evidence that glioma has a slight male predominance implies that factors associated with sex hormones may play a role in the development of glioma. The association between oral contraceptive (OC) use and glioma risk remains controversial. METHOD: In the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial of 70,516 women in the USA, Cox proportional hazards regression analyses were adopted to calculate the crude and adjusted hazard ratios (HRs) and 95% confidence intervals (CIs). Additionally, a meta-analysis combining the PLCO findings with those of other prospective cohorts was performed. RESULTS: During a mean follow-up of ~11.7 years, 110 of 70,516 women aged 50–78 years at baseline were diagnosed with glioma in PLCO studies. Compared with never users, an inverse association of borderline significance was found for OC users (HR 0.67, 95% CI 0.44–1.04, P = 0.074). Analyses assessing glioma risk according to the duration of OC use yielded no significant association. When PLCO was combined with four other prospective studies, there was an inverse association between OC use and glioma risk (HR 0.85, 95% CI 0.75–0.97, I(2) = 0.0%). Further dose-response analysis showed a nonlinear, inverse relationship between OC use and glioma risk (P < 0.001). CONCLUSIONS: This study provided some evidence of a nonlinear, inverse association between OC use and glioma risk. Future larger studies are warranted to validate this finding. Frontiers Media S.A. 2022-07-14 /pmc/articles/PMC9330220/ /pubmed/35910887 http://dx.doi.org/10.3389/fpubh.2022.878233 Text en Copyright © 2022 Shao, Tang, Wang, He, Wang and Wu. https://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) and the copyright owner(s) 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 Public Health
Shao, Chuan
Tang, Hui
Wang, Xiaoya
He, Jiaquan
Wang, Pan
Wu, Nan
Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis
title Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis
title_full Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis
title_fullStr Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis
title_full_unstemmed Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis
title_short Oral Contraceptive and Glioma Risk: A Prospective Cohort Study and Meta-Analysis
title_sort oral contraceptive and glioma risk: a prospective cohort study and meta-analysis
topic Public Health
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9330220/
https://www.ncbi.nlm.nih.gov/pubmed/35910887
http://dx.doi.org/10.3389/fpubh.2022.878233
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