Institute of Epidemiology and Medical Biometry, Ulm University, Ulm, Germany.
Agency for Preventive and Social Medicine (aks), Bregenz, Austria.
Int J Cancer. 2021 Jul 1;149(1):66-74. doi: 10.1002/ijc.33530. Epub 2021 Mar 4.
To explore the largely unknown etiology of small intestine cancer, we examined metabolic factors and risk of small intestine cancer overall and by subtypes. Among 404 220 women and 403 265 men in six European cohorts, we applied Cox regression with adjustment for smoking and body mass index (BMI), to calculate sex-specific hazard ratios (HRs) of small intestine cancer by levels of BMI, mean arterial pressure (MAP) and plasma total cholesterol, triglycerides and glucose. We also calculated HRs for these factors combined (metabolic score; MetS) and used Wald test statistics to investigate pairwise interactions between metabolic factors on risk. We also performed analyses separately per subtype (neuroendocrine tumors [NETs] and adenocarcinomas). During a median follow-up of 16.9 years, 144 women and 195 men were diagnosed with small intestine cancer, including 184 NETs and 99 adenocarcinomas. Among men, no main associations or interactions between metabolic factors were observed in relation to the risk of small intestine cancer. Among women, triglycerides were positively and linearly associated with risk (HR per standard deviation [SD]: 1.23, 95% confidence interval [CI]: 1.04-1.46), and a positive association was also observed for the MetS (HR per SD: 1.25, 95% CI: 1.02-1.52). Positive interactions were observed among women between triglycerides and cholesterol (P = .0005), and between MAP and glucose (P = .009), on risk. Glucose was positively associated with adenocarcinomas among women. This large, prospective study suggests that elevated triglycerides, and metabolic factors in interaction, confer an increased risk of small intestine cancer among women, but not among men.
为了探索小肠癌发病机制中尚未阐明的因素,我们研究了代谢因素与小肠癌总体及各亚型发病风险的相关性。在欧洲六个队列的 404220 名女性和 403265 名男性中,我们应用 Cox 比例风险回归模型,通过 BMI、平均动脉压(MAP)和血浆总胆固醇、甘油三酯和葡萄糖水平,对小肠癌发病风险进行了校正后计算性别特异性危险比(HR)。我们还计算了这些因素联合的 HR(代谢评分;MetS),并采用 Wald 检验统计量来评估代谢因素之间的交互作用。我们还分别按亚型(神经内分泌肿瘤 [NET] 和腺癌)进行了分析。中位随访 16.9 年后,144 名女性和 195 名男性被诊断患有小肠癌,其中包括 184 例 NET 和 99 例腺癌。在男性中,未观察到代谢因素与小肠癌风险之间存在主要相关性或相互作用。在女性中,甘油三酯与风险呈正相关且呈线性关系(每标准差 HR:1.23,95%置信区间 [CI]:1.04-1.46),代谢评分也呈正相关(每 SD HR:1.25,95% CI:1.02-1.52)。在女性中,还观察到甘油三酯和胆固醇(P =.0005)以及 MAP 和葡萄糖(P =.009)之间存在正交互作用。在女性中,葡萄糖与腺癌呈正相关。这项大型前瞻性研究表明,在女性中,甘油三酯升高以及代谢因素相互作用与小肠癌风险增加相关,但在男性中则不然。