Sadr-Azodi Omid, Konings Peter, Brusselaers Nele
Clinical Epidemiology Unit, Department of Medicine Solna, Karolinska Institutet, Stockholm, Sweden.
Department of Surgery, Eskilstuna County Hospital, Eskilstuna, Sweden.
United European Gastroenterol J. 2017 Dec;5(8):1123-1128. doi: 10.1177/2050640617702060. Epub 2017 Apr 9.
The role of menopausal hormone therapy (MHT) in the development of pancreatic cancer is inconclusive owing to small studies and lack of proper study design.
This population-based matched cohort study included all Swedish women who used systemic MHT between 1 July 2005 and 31 December 2012. For each user of MHT, three never-users of MHT were randomly selected, matched for childbirth, history of thromboembolic events, and previous hysterectomy, as well as for year of birth, diabetes, obesity, and smoking- or alcohol-related disorders. Multivariable conditional logistic regression was used to calculate odds ratios (ORs) and 95% confidence intervals (CIs) for the association between MHT use and pancreatic cancer. The effect of MHT duration on pancreatic cancer development was calculated using multivariable Poisson regression.
There were 290,186 ever-users of MHT and 870,165 matched never-users. During the follow-up, 311 (0.0011%) ever-users of MHT and 1220 (0.0014) never-users developed pancreatic cancer. In a multivariable adjusted model, ever-users had a 23% reduced risk (OR 0.77; 95% CI: 0.68-0.87) of pancreatic cancer. This risk decreased by 35% (incidence rate ratio (IRR) 0.65; 95% CI: 0.33-1.27) in women who used MHT 1-2 years and by 60% (IRR 0.40; 95% CI: 0.18-0.88) in women who used MHT ≥ 3 years compared to women with <1 year of MHT use. The type of MHT did not change the results.
Systemic MHT use might reduce the risk of pancreatic cancer.
由于研究规模小且缺乏恰当的研究设计,绝经激素治疗(MHT)在胰腺癌发生中的作用尚无定论。
这项基于人群的匹配队列研究纳入了2005年7月1日至2012年12月31日期间使用系统性MHT的所有瑞典女性。对于每位MHT使用者,随机选取三名从未使用过MHT的女性,在分娩、血栓栓塞事件史、既往子宫切除术以及出生年份、糖尿病、肥胖、吸烟或酒精相关疾病方面进行匹配。采用多变量条件逻辑回归计算MHT使用与胰腺癌之间关联的比值比(OR)和95%置信区间(CI)。使用多变量泊松回归计算MHT使用时长对胰腺癌发生的影响。
共有290,186名MHT使用者和870,165名匹配的非使用者。在随访期间,311名(0.0011%)MHT使用者和1220名(0.0014%)非使用者患胰腺癌。在多变量调整模型中,MHT使用者患胰腺癌的风险降低了23%(OR 0.77;95% CI:0.68 - 0.87)。与使用MHT不足1年的女性相比,使用MHT 1 - 2年的女性风险降低了35%(发病率比(IRR)0.65;95% CI:0.33 - 1.27),使用MHT≥3年的女性风险降低了60%(IRR 0.40;95% CI:0.18 - 0.88)。MHT的类型不影响结果。
使用系统性MHT可能降低患胰腺癌的风险。