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Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study

BACKGROUND: The role of exogenous hormone exposures in the development of meningioma is unclear, but these exposures have been proposed as one hypothesis to explain the over-abundance of such tumors in women. METHODS: The association between oral contraception (OC) or hormone replacement therapy (HR...

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Autores principales: Custer, Brian, Longstreth, WT, Phillips, Leslie E, Koepsell, Thomas D, Van Belle, Gerald
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524800/
https://www.ncbi.nlm.nih.gov/pubmed/16759391
http://dx.doi.org/10.1186/1471-2407-6-152
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author Custer, Brian
Longstreth, WT
Phillips, Leslie E
Koepsell, Thomas D
Van Belle, Gerald
author_facet Custer, Brian
Longstreth, WT
Phillips, Leslie E
Koepsell, Thomas D
Van Belle, Gerald
author_sort Custer, Brian
collection PubMed
description BACKGROUND: The role of exogenous hormone exposures in the development of meningioma is unclear, but these exposures have been proposed as one hypothesis to explain the over-abundance of such tumors in women. METHODS: The association between oral contraception (OC) or hormone replacement therapy (HRT) and intracranial meningioma in women was investigated using a population-based, matched case-control study. Exposures for 143 cases and 286 controls matched on age within five years were obtained by interview. Diagnoses were confirmed histopathologically and estrogen and progesterone receptor assays conducted. RESULTS: Although risk of meningioma appeared modestly elevated in past OC users (OR = 1.5, 95% CI 0.8 – 2.7), and in current users (OR = 2.5, 95% CI 0.5 – 12.6), the confidence intervals were wide. No significant association between meningioma risk and duration of OC use was found. Likewise, risk of meningioma was only weakly associated with past use of HRT (OR = 0.7, 95% CI 0.4 – 1.3), and not at all with current use of HRT (OR = 1.0, 95% CI 0.5 – 2.2). Of 142 available specimens, 2 (1%) expressed estrogen receptors, whereas 130 (92%) expressed progesterone receptors (PR). OC use was associated with increased risk of a meningioma expressing less rather than more PR (OR = 3.2, 95% CI 1.3 – 8.0). Overall, in post menopausal women, HRT use appeared to confer a non-significant protective effect, and was not associated with low or high PR expressing meningiomas. CONCLUSION: This study found little evidence of associations between meningioma and exogenous hormone exposures in women but did suggest that some hormonal exposures may influence tumor biology in those women who develop meningioma.
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spelling pubmed-15248002006-07-29 Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study Custer, Brian Longstreth, WT Phillips, Leslie E Koepsell, Thomas D Van Belle, Gerald BMC Cancer Research Article BACKGROUND: The role of exogenous hormone exposures in the development of meningioma is unclear, but these exposures have been proposed as one hypothesis to explain the over-abundance of such tumors in women. METHODS: The association between oral contraception (OC) or hormone replacement therapy (HRT) and intracranial meningioma in women was investigated using a population-based, matched case-control study. Exposures for 143 cases and 286 controls matched on age within five years were obtained by interview. Diagnoses were confirmed histopathologically and estrogen and progesterone receptor assays conducted. RESULTS: Although risk of meningioma appeared modestly elevated in past OC users (OR = 1.5, 95% CI 0.8 – 2.7), and in current users (OR = 2.5, 95% CI 0.5 – 12.6), the confidence intervals were wide. No significant association between meningioma risk and duration of OC use was found. Likewise, risk of meningioma was only weakly associated with past use of HRT (OR = 0.7, 95% CI 0.4 – 1.3), and not at all with current use of HRT (OR = 1.0, 95% CI 0.5 – 2.2). Of 142 available specimens, 2 (1%) expressed estrogen receptors, whereas 130 (92%) expressed progesterone receptors (PR). OC use was associated with increased risk of a meningioma expressing less rather than more PR (OR = 3.2, 95% CI 1.3 – 8.0). Overall, in post menopausal women, HRT use appeared to confer a non-significant protective effect, and was not associated with low or high PR expressing meningiomas. CONCLUSION: This study found little evidence of associations between meningioma and exogenous hormone exposures in women but did suggest that some hormonal exposures may influence tumor biology in those women who develop meningioma. BioMed Central 2006-06-07 /pmc/articles/PMC1524800/ /pubmed/16759391 http://dx.doi.org/10.1186/1471-2407-6-152 Text en Copyright © 2006 Custer et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Custer, Brian
Longstreth, WT
Phillips, Leslie E
Koepsell, Thomas D
Van Belle, Gerald
Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study
title Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study
title_full Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study
title_fullStr Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study
title_full_unstemmed Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study
title_short Hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study
title_sort hormonal exposures and the risk of intracranial meningioma in women: a population-based case-control study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1524800/
https://www.ncbi.nlm.nih.gov/pubmed/16759391
http://dx.doi.org/10.1186/1471-2407-6-152
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