TY - JOUR
T1 - Hormonal contraceptive use and risk of glioma among younger women a nationwide case-control study
AU - Andersen, Lene
AU - Friis, Søren
AU - Hallas, Jesper
AU - Ravn, Pernille
AU - Kristensen, Bjarne W
AU - Gaist, David
N1 - This article is protected by copyright. All rights reserved.
PY - 2015/4
Y1 - 2015/4
N2 - Aim Oral contraceptive use influences the risk for certain cancers. However, few studies have examined any link with risk of central nervous system tumours. We investigated the association between hormonal contraceptive use and glioma risk among premenopausal women in a population-based setting. Methods Using national administrative and health registries in Denmark to conduct a nationwide case-control study, we identified all women ages 15 to 49 years with a first time diagnosis of histologically verified glioma between 2000 and 2009. Each case was age-matched to eight population controls using risk set sampling. Based on prescription data, exposure until 2 years prior to the index date was categorized according to hormonal contraceptive type, i.e. combined oestrogen-progestagen or progestagen only, and duration of use (<1, 1 to <5, ≥5 years). We used conditional logistic regression to compute odds ratios (ORs) with 95% confidence intervals (CIs) for glioma associated with hormonal contraceptive use, adjusting for potential confounders. Results We identified 317 cases and 2126 controls. Ever use of hormonal contraceptive was associated with an OR of 1.5 (95% CI 1.2, 2.0) and the OR increased with duration of use (long term, ≥5 years: OR 1.9; 95% CI 1.2, 2.9). The association between long term hormonal contraceptive use and glioma risk was most pronounced for progestagen only therapy (OR 2.4; 95% CI 1.1, 5.1), especially when this regimen constituted the sole hormonal contraceptive therapy (OR 4.1; 95% CI 0.8, 20.8). Conclusion Long term hormonal contraceptive use may increase the risk of glioma.
AB - Aim Oral contraceptive use influences the risk for certain cancers. However, few studies have examined any link with risk of central nervous system tumours. We investigated the association between hormonal contraceptive use and glioma risk among premenopausal women in a population-based setting. Methods Using national administrative and health registries in Denmark to conduct a nationwide case-control study, we identified all women ages 15 to 49 years with a first time diagnosis of histologically verified glioma between 2000 and 2009. Each case was age-matched to eight population controls using risk set sampling. Based on prescription data, exposure until 2 years prior to the index date was categorized according to hormonal contraceptive type, i.e. combined oestrogen-progestagen or progestagen only, and duration of use (<1, 1 to <5, ≥5 years). We used conditional logistic regression to compute odds ratios (ORs) with 95% confidence intervals (CIs) for glioma associated with hormonal contraceptive use, adjusting for potential confounders. Results We identified 317 cases and 2126 controls. Ever use of hormonal contraceptive was associated with an OR of 1.5 (95% CI 1.2, 2.0) and the OR increased with duration of use (long term, ≥5 years: OR 1.9; 95% CI 1.2, 2.9). The association between long term hormonal contraceptive use and glioma risk was most pronounced for progestagen only therapy (OR 2.4; 95% CI 1.1, 5.1), especially when this regimen constituted the sole hormonal contraceptive therapy (OR 4.1; 95% CI 0.8, 20.8). Conclusion Long term hormonal contraceptive use may increase the risk of glioma.
KW - brain tumour epidemiology
KW - case-control study
KW - glioma
KW - hormonal contraceptive
KW - risk
KW - Humans
KW - Middle Aged
KW - Risk
KW - Case-Control Studies
KW - Young Adult
KW - Contraceptives, Oral, Hormonal/adverse effects
KW - Denmark/epidemiology
KW - Adolescent
KW - Adult
KW - Female
KW - Odds Ratio
KW - Brain Neoplasms/chemically induced
KW - Glioma/chemically induced
U2 - 10.1111/bcp.12535
DO - 10.1111/bcp.12535
M3 - Journal article
C2 - 25345919
SN - 0306-5251
VL - 79
SP - 677
EP - 684
JO - British Journal of Clinical Pharmacology
JF - British Journal of Clinical Pharmacology
IS - 4
ER -