Jacobson Sara, Dahlqvist Per, Johansson Mattias, Svensson Johan, Billing Ola, Sund Malin, Franklin Oskar
Department of Surgical and Perioperative Sciences, Surgery, Umeå University, Umeå, Sweden.
Department of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Pancreatology. 2021 Sep;21(6):1112-1118. doi: 10.1016/j.pan.2021.05.008. Epub 2021 May 15.
To determine the risk association between fasting glucose levels and pancreatic cancer using systematically collected prediagnostic blood glucose samples.
Prospective nested case-control study of participants from the Northern Sweden Health and Disease Study, including 182 cases that developed pancreatic cancer and four matched controls per case. Blood glucose levels collected up to 24 years before pancreatic cancer diagnosis were analyzed. The association between fasting glucose levels and pancreatic cancer risk was determined using unconditional and conditional logistic regression models. The association between fasting glucose and the time to pancreatic cancer diagnosis, tumor stage and survival was determined using likelihood-ratio test, t-test and log rank test.
The unadjusted risk of developing pancreatic cancer increased with increasing fasting glucose levels (OR 1.30, 95% CI 1.05-1.60, P = .015). Impaired fasting glucose (≥6.1 mmol/L) was associated with an adjusted risk of 1.77 for developing pancreatic cancer (95% CI 1.05-2.99, P = .032). In subgroup analysis, fasting glucose levels were associated with an increased risk in never-smokers (OR 4.02, 95% CI 1.26-12.77, P = .018) and non-diabetics (OR 3.08, 95% CI 1.08-8.79, P = .035) (non-significant for interaction). The ratio between fasting glucose and BMI was higher among future pancreatic cancer patients and an increased ratio was associated with elevated risk of pancreatic cancer (OR 1.66, 95% CI 1.04-2.66, P = .034). Fasting glucose levels were not associated with TNM stage at diagnosis or survival.
High fasting glucose is associated with an increased risk of being diagnosed with pancreatic cancer.
利用系统收集的诊断前血糖样本确定空腹血糖水平与胰腺癌之间的风险关联。
对来自瑞典北部健康与疾病研究的参与者进行前瞻性巢式病例对照研究,包括182例患胰腺癌的病例以及每例病例匹配的4名对照。分析了在胰腺癌诊断前长达24年收集的血糖水平。使用无条件和条件逻辑回归模型确定空腹血糖水平与胰腺癌风险之间的关联。使用似然比检验、t检验和对数秩检验确定空腹血糖与胰腺癌诊断时间、肿瘤分期及生存之间的关联。
未调整的患胰腺癌风险随空腹血糖水平升高而增加(比值比1.30,95%置信区间1.05 - 1.60,P = 0.015)。空腹血糖受损(≥6.1 mmol/L)与患胰腺癌的调整后风险1.77相关(95%置信区间1.05 - 2.99,P = 0.032)。在亚组分析中,空腹血糖水平与从不吸烟者(比值比4.02,95%置信区间1.26 - 12.77,P = 0.018)和非糖尿病患者(比值比3.08,95%置信区间1.08 - ⑧)患胰腺癌风险增加相关(交互作用无统计学意义)。未来胰腺癌患者的空腹血糖与体重指数之比更高,该比值增加与胰腺癌风险升高相关(比值比1.66,95%置信区间1.04 - 2.66,P = 0.034)。空腹血糖水平与诊断时TNM分期或生存无关。
高空腹血糖与被诊断为胰腺癌的风险增加相关。