Department of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Department of Behavioral Science, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer Prev Res (Phila). 2018 Aug;11(8):477-490. doi: 10.1158/1940-6207.CAPR-17-0398. Epub 2018 May 1.
Obesity increases risk of endometrial cancer through dysregulation of estrogen and insulin signaling. The primary aim of this study was to evaluate the impact of metformin or lifestyle intervention on endometrial proliferation in postmenopausal obese women. Secondary aims included evaluating obesity-related biomarkers and adverse events experienced. Obese, postmenopausal women with prediabetes were randomized into four groups for a 16-week intervention using a 2 (metformin 1700 mg/day vs. placebo) × 2 (lifestyle intervention vs. no lifestyle intervention) factorial design. Pre- and postintervention endometrial proliferation, anthropometrics, body composition, and serum biomarkers (sex hormones, sex hormone binding globulin, IGF-I, adiponectin, omentin, insulin, glucose, and others) were assessed. Data were analyzed with linear regression models and false-discovery rate correction. Of 576 women approached for the study, 52 attended initial screening, 29 were eligible and randomized, and 26 completed the study. Lifestyle intervention resulted in significant loss of weight (-4.23 kg, = 0.006) and total fat mass (-3.23 kg, < 0.001). Participants receiving metformin lost 3.43 kg of weight ( = 0.023), but this was not statistically significant after multiple comparisons adjustment controlling false-discovery rate to 10%. Endometrial proliferation was low at baseline (mean 7.1%) and remained unchanged by 16 weeks, but included substantial variability. Metformin and lifestyle intervention produced minor changes to serum biomarkers. Lifestyle intervention produced the most significant changes in weight and body composition. While it is known that obese postmenopausal women are at increased risk for endometrial cancer, improved biomarkers are needed to stratify risk and test prevention strategies, particularly at the endometrial tissue level. .
肥胖通过雌激素和胰岛素信号的失调增加子宫内膜癌的风险。本研究的主要目的是评估二甲双胍或生活方式干预对绝经后肥胖妇女子宫内膜增殖的影响。次要目的包括评估肥胖相关生物标志物和经历的不良事件。患有糖尿病前期的绝经后肥胖妇女随机分为四组,进行为期 16 周的干预,采用 2(二甲双胍 1700mg/天与安慰剂)×2(生活方式干预与无生活方式干预)析因设计。评估了干预前后的子宫内膜增殖、人体测量学、身体成分和血清生物标志物(性激素、性激素结合球蛋白、IGF-I、脂联素、网膜素、胰岛素、葡萄糖和其他)。使用线性回归模型和错误发现率校正进行数据分析。在 576 名接受研究的妇女中,有 52 名参加了初步筛选,29 名符合条件并被随机分组,26 名完成了研究。生活方式干预导致体重显著下降(-4.23kg, = 0.006)和总脂肪量减少(-3.23kg, < 0.001)。接受二甲双胍治疗的患者体重减轻 3.43kg( = 0.023),但在经过多次比较调整控制错误发现率至 10%后,这一结果并不具有统计学意义。子宫内膜增殖在基线时较低(平均 7.1%),16 周后保持不变,但存在较大的变异性。二甲双胍和生活方式干预对血清生物标志物的影响较小。生活方式干预对体重和身体成分的影响最为显著。虽然已知绝经后肥胖妇女患子宫内膜癌的风险增加,但需要改善生物标志物来分层风险并测试预防策略,特别是在子宫内膜组织水平。