Kabat Geoffrey C, Kim Mimi Y, Lane Dorothy S, Zaslavsky Oleg, Ho Gloria Y F, Luo Juhua, Nicholson Wanda K, Chlebowski Rowan T, Barrington Wendy E, Vitolins Mara Z, Lin Xiaochen, Liu Simin, Rohan Thomas E
Department of Epidemiology and Population Health, Albert Einstein College of Medicine, Bronx.
Department of Preventive Medicine, Stony Brook University, Stony Brook.
Eur J Cancer Prev. 2018 May;27(3):261-268. doi: 10.1097/CEJ.0000000000000435.
Limited evidence suggests that hyperinsulinemia may contribute to the risk of breast, endometrial, and, possibly, ovarian cancer. The aim of this study was to assess the association of serum glucose and insulin with risk of these cancers in postmenopausal women, while taking into account potential confounding and modifying factors. We studied 21 103 women with fasting baseline insulin and glucose measurements in a subsample of the Women's Health Initiative. The subsample was composed of four studies within Women's Health Initiative with different selection and sampling strategies. Over a mean of 14.7 years of follow-up, 1185 breast cancer cases, 156 endometrial cancer cases, and 130 ovarian cancer cases were diagnosed. We used Cox proportional hazards models to estimate hazard ratios (HRs) and 95% confidence intervals (95% CIs) by quartile of glucose or insulin. Serum insulin was positively associated with breast cancer risk (multivariable-adjusted HR for highest vs. lowest quartile 1.41, 95% CI: 1.16-1.72, Ptrend<0.0003), and glucose and insulin were associated with roughly a doubling of endometrial cancer risk (for glucose: HR: 2.00, 95% CI: 1.203.35, Ptrend=0.01; for insulin: HR: 2.39, 95% CI: 1.32-4.33, Ptrend=0.008). These associations remained unchanged or were slightly attenuated after mutual adjustment, adjustment for serum lipids, and assessment of possible reverse causation. Glucose and insulin showed no association with ovarian cancer. Our findings provide support for a role of insulin-related pathways in the etiology of cancers of the breast and endometrium. However, because of the unrepresentative nature of the sample, our results need confirmation in other populations.
有限的证据表明,高胰岛素血症可能会增加患乳腺癌、子宫内膜癌以及可能的卵巢癌的风险。本研究的目的是评估绝经后女性血清葡萄糖和胰岛素与这些癌症风险之间的关联,同时考虑潜在的混杂因素和修正因素。我们在女性健康倡议的一个子样本中研究了21103名有空腹基线胰岛素和葡萄糖测量值的女性。该子样本由女性健康倡议中的四项研究组成,这些研究采用了不同的选择和抽样策略。在平均14.7年的随访期内,诊断出1185例乳腺癌病例、156例子宫内膜癌病例和130例卵巢癌病例。我们使用Cox比例风险模型,按葡萄糖或胰岛素四分位数估计风险比(HR)和95%置信区间(95%CI)。血清胰岛素与乳腺癌风险呈正相关(最高四分位数与最低四分位数的多变量调整HR为1.41,95%CI:1.16 - 1.72,Ptrend<0.0003),葡萄糖和胰岛素与子宫内膜癌风险大致翻倍有关(葡萄糖:HR:2.00,95%CI:1.20 - 3.35,Ptrend = 0.01;胰岛素:HR:2.39,95%CI:1.32 - 4.33,Ptrend = 0.008)。在相互调整、调整血清脂质以及评估可能的反向因果关系后,这些关联保持不变或略有减弱。葡萄糖和胰岛素与卵巢癌无关联。我们的研究结果支持胰岛素相关途径在乳腺癌和子宫内膜癌病因学中的作用。然而,由于样本的非代表性,我们的结果需要在其他人群中得到证实。