Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.
Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Cancer Epidemiol Biomarkers Prev. 2021 Feb;30(2):335-343. doi: 10.1158/1055-9965.EPI-20-0764. Epub 2020 Nov 20.
We investigated the associations of postdiagnostic dietary glycemic index (GI), glycemic load (GL), insulin index (II), and insulin load (IL) with breast cancer-specific and all-cause mortality.
Among 8,932 women with stage I-III breast cancer identified in the Nurses' Health Study (NHS; 1980-2010) and NHSII (1991-2011), we prospectively evaluated the associations between postdiagnostic GI, GL, II, and IL, and breast cancer-specific and all-cause mortality. Participants completed a validated food frequency questionnaire every 4 years after diagnosis.
During follow-up by 2014 in the NHS and 2015 in the NHSII, 2,523 deaths, including 1,071 from breast cancer, were documented. Higher postdiagnostic GL was associated with higher risk of both breast cancer-specific mortality [HR = 1.33; 95% confidence interval (CI) = 1.09-1.63; = 0.008] and all-cause mortality (HR = 1.26; 95% CI = 1.10-1.45; = 0.0006). Higher all-cause mortality was also observed with higher postdiagnostic GI (HR = 1.23; 95% CI = 1.08-1.40; = 0.001), II (HR = 1.20; 95% CI = 1.04-1.38; = 0.005), and IL (HR = 1.23; 95% CI = 1.07-1.42; = 0.0003). The associations were not modified by insulin receptor or estrogen receptor status of the tumor, or body mass index.
We found that higher dietary GL, reflecting postprandial glucose response, after a breast cancer diagnosis was associated with higher risk of breast cancer-specific mortality. Higher dietary GI, GL, II, and IL after a breast cancer diagnosis were associated with higher risk of death from any cause.
These results suggest that carbohydrate quantity and quality may be important in breast cancer prognosis..
我们研究了诊断后饮食血糖指数(GI)、血糖负荷(GL)、胰岛素指数(II)和胰岛素负荷(IL)与乳腺癌特异性和全因死亡率的关联。
在护士健康研究(NHS;1980-2010 年)和 NHSII(1991-2011 年)中,我们前瞻性评估了诊断后 GI、GL、II 和 IL 与乳腺癌特异性和全因死亡率之间的关系。参与者在诊断后每 4 年完成一次验证后的食物频率问卷。
在 NHS 的随访至 2014 年和 NHSII 的随访至 2015 年期间,共记录了 2523 例死亡,其中 1071 例死于乳腺癌。较高的诊断后 GL 与乳腺癌特异性死亡率升高相关[风险比(HR)=1.33;95%置信区间(CI)=1.09-1.63;P=0.008]和全因死亡率升高相关(HR=1.26;95%CI=1.10-1.45;P=0.0006)。较高的全因死亡率也与较高的诊断后 GI(HR=1.23;95%CI=1.08-1.40;P=0.001)、II(HR=1.20;95%CI=1.04-1.38;P=0.005)和 IL(HR=1.23;95%CI=1.07-1.42;P=0.0003)相关。这些关联不受肿瘤胰岛素受体或雌激素受体状态或体重指数的影响。
我们发现,乳腺癌诊断后较高的饮食 GL,反映了餐后血糖反应,与乳腺癌特异性死亡率升高相关。乳腺癌诊断后较高的饮食 GI、GL、II 和 IL 与任何原因导致的死亡风险增加相关。
这些结果表明,碳水化合物的数量和质量可能在乳腺癌的预后中很重要。