Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Pituitary/Neuroendocrine Center, Department of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
J Clin Endocrinol Metab. 2022 Mar 24;107(4):e1402-e1412. doi: 10.1210/clinem/dgab868.
No prospective epidemiologic studies have examined associations between use of oral contraceptives (OCs) or menopausal hormone therapy (MHT) and risk of pituitary adenoma in women.
Our aim was to determine the association between use of OC and MHT and risk of pituitary adenoma in two separate datasets.
We evaluated the association of OC/MHT with risk of pituitary adenoma in the Nurses' Health Study and Nurses' Health Study II by computing multivariable-adjusted hazard ratios (MVHR) of pituitary adenoma by OC/MHT use using Cox proportional hazards models. Simultaneously, we carried out a matched case-control study using an institutional data repository to compute multivariable-adjusted odds ratios (MVOR) of pituitary adenoma by OC/MHT use.
In the cohort analysis, during 6 668 019 person-years, 331 participants reported a diagnosis of pituitary adenoma. Compared to never-users, neither past (MVHR = 1.05; 95% CI, 0.80-1.36) nor current OC use (MVHR = 0.72; 95% CI, 0.40-1.32) was associated with risk. For MHT, compared to never-users, both past (MVHR = 2.00; 95% CI, 1.50-2.68) and current use (MVHR = 1.80; 95% CI, 1.27-2.55) were associated with pituitary adenoma risk, as was longer duration (MVHR = 2.06; 95% CI, 1.42-2.99 comparing more than 5 years of use to never, P trend = .002). Results were similar in lagged analyses, when stratified by body mass index, and among those with recent health care use. In the case-control analysis, we included 5469 cases. Risk of pituitary adenoma was increased with ever use of MHT (MVOR = 1.57; 95% CI, 1.35-1.83) and OC (MVOR = 1.27; 95% CI, 1.14-1.42) compared to never.
Compared to never use, current and past MHT use and longer duration of MHT use were positively associated with higher risk of pituitary adenoma in 2 independent data sets. OC use was not associated with risk in the prospective cohort analysis and was associated with only mildly increased risk in the case-control analysis.
尚无前瞻性流行病学研究探讨口服避孕药(OC)或绝经激素治疗(MHT)的使用与女性垂体腺瘤风险之间的关系。
我们旨在通过 Cox 比例风险模型计算 OC/MHT 使用与垂体腺瘤风险的多变量调整后的危害比(MVHR),在两个独立数据集之间确定 OC 和 MHT 使用与垂体腺瘤风险之间的关联。同时,我们利用机构数据存储库进行了一项病例对照研究,以计算 OC/MHT 使用与垂体腺瘤风险的多变量调整后的比值比(MVOR)。
我们通过计算 MVHR 评估了 OC/MHT 与护士健康研究和护士健康研究 II 中垂体腺瘤风险的关联,MVHR 是通过 OC/MHT 使用的垂体腺瘤风险。同时,我们利用机构数据存储库进行了一项匹配病例对照研究,以计算 OC/MHT 使用与垂体腺瘤风险的多变量调整比值比(MVOR)。
在队列分析中,在 6668019 人年期间,有 331 名参与者报告了垂体腺瘤的诊断。与从未使用者相比,过去(MVHR=1.05;95%CI,0.80-1.36)或当前 OC 使用(MVHR=0.72;95%CI,0.40-1.32)均与风险无关。对于 MHT,与从未使用者相比,过去(MVHR=2.00;95%CI,1.50-2.68)和当前使用(MVHR=1.80;95%CI,1.27-2.55)均与垂体腺瘤风险相关,使用时间较长(MVHR=2.06;95%CI,1.42-2.99,与从未使用相比,P 趋势=0.002)。在滞后分析中,当按体重指数分层和在最近有医疗保健使用的人群中,结果相似。在病例对照分析中,我们纳入了 5469 例病例。与从未使用者相比,MHT(MVOR=1.57;95%CI,1.35-1.83)和 OC(MVOR=1.27;95%CI,1.14-1.42)的任何使用都与垂体腺瘤风险增加相关。
与从未使用相比,当前和过去的 MHT 使用以及 MHT 使用时间较长与两个独立数据集的更高垂体腺瘤风险呈正相关。在前瞻性队列分析中,OC 使用与风险无关,而在病例对照分析中仅与风险呈轻度增加相关。