Clendenen Tess V, Hertzmark Kathryn, Koenig Karen L, Lundin Eva, Rinaldi Sabina, Johnson Theron, Krogh Vittorio, Hallmans Göran, Idahl Annika, Lukanova Annekatrin, Zeleniuch-Jacquotte Anne
Department of Population Health, Division of Epidemiology and Biostatistics, New York University School of Medicine, 650 1st Ave, New York, NY, 10016, USA.
Department of Environmental Medicine, Division of Epidemiology and Biostatistics, New York University School of Medicine, New York, NY, USA.
Horm Cancer. 2016 Jun;7(3):178-87. doi: 10.1007/s12672-016-0258-1. Epub 2016 Feb 29.
Endometrial cancer risk is increased by estrogens unopposed by progesterone. In premenopausal women, androgen excess is often associated with progesterone insufficiency, suggesting that premenopausal androgen concentrations may be associated with risk. In a case-control study nested within three cohorts, we assessed the relationship between premenopausal androgens and risk of endometrial cancer (161 cases and 303 controls matched on age and date of blood donation). Testosterone, DHEAS, androstenedione, and SHBG were measured in serum or plasma. Free testosterone was calculated from testosterone and SHBG. We observed trends of increasing risk across tertiles of testosterone (ORT3-T1 = 1.59, 95 % CI = 0.96, 2.64, p = 0.08) and free testosterone (ORT3-T1 = 1.76, 95 % CI = 1.01, 3.07, p = 0.047), which were not statistically significant after adjustment for body mass index (BMI). There was no association for DHEAS, androstenedione, or SHBG. There were significant interactions by age at diagnosis (<55 years, n = 51 cases; ≥55 years, n = 110 cases). Among women who were ≥55 years of age (predominantly postmenopausal) at diagnosis, the BMI-adjusted OR was 2.08 (95 % CI = 1.25, 3.44, p = 0.005) for a doubling in testosterone and 1.55 (95 % CI = 1.04, 2.31, p = 0.049) for a doubling in free testosterone. There was no association among women aged <55 years at diagnosis, consistent with the only other prospective study to date. If pre- and post-menopausal concentrations of androgens are correlated, our observation of an association of premenopausal androgens with risk among women aged ≥55 years at diagnosis could be due to the effect on the endometrium of postmenopausal androgen-derived estrogens in the absence of progesterone, which is no longer secreted.
未受孕激素拮抗的雌激素会增加子宫内膜癌风险。在绝经前女性中,雄激素过多常与孕激素不足相关,这表明绝经前雄激素浓度可能与风险有关。在一项嵌套于三个队列的病例对照研究中,我们评估了绝经前雄激素与子宫内膜癌风险之间的关系(161例病例和303例按年龄和献血日期匹配的对照)。测定血清或血浆中的睾酮、硫酸脱氢表雄酮、雄烯二酮和性激素结合球蛋白。游离睾酮由睾酮和性激素结合球蛋白计算得出。我们观察到睾酮三分位数(三分位数3 - 三分位数1的比值比=1.59,95%置信区间=0.96,2.64,p = 0.08)和游离睾酮三分位数(三分位数3 - 三分位数1的比值比=1.76,95%置信区间=1.01,3.07,p = 0.047)的风险呈上升趋势,在调整体重指数(BMI)后这些趋势无统计学意义。硫酸脱氢表雄酮、雄烯二酮或性激素结合球蛋白无关联。诊断时年龄存在显著交互作用(<55岁,51例病例;≥55岁,110例病例)。在诊断时年龄≥55岁(主要为绝经后)的女性中,睾酮翻倍时经BMI调整的比值比为2.08(95%置信区间=1.25,3.44,p = 0.005),游离睾酮翻倍时为1.55(95%置信区间=1.04,2.31,p = 0.049)。在诊断时年龄<55岁的女性中无关联,这与迄今为止唯一的另一项前瞻性研究一致。如果绝经前和绝经后雄激素浓度相关,那么我们观察到的诊断时年龄≥55岁女性中绝经前雄激素与风险的关联可能是由于在不再分泌孕激素的情况下,绝经后雄激素衍生的雌激素对子宫内膜的影响。