Department of Epidemiology and Health Statistics, School of Public Health, Lanzhou University, 199 Donggang West Street, Lanzhou, Gansu, China.
Eur J Cancer Prev. 2024 Jul 1;33(4):347-354. doi: 10.1097/CEJ.0000000000000863. Epub 2023 Nov 13.
To evaluate the correlation between metabolic syndrome (MetS) and its components on the incidence of colorectal cancer (CRC) based on data from Jinchang Cohort.
This is a large prospective cohort study. Between 2011 and 2020, a total of 43 516 individuals from Jinchang Cohort were included for this study. Hazard ratios (HRs) with 95% confidence intervals (CIs) for CRC according to MetS were calculated with the Cox proportional hazard models. The restricted cubic spine models with four knots were conducted to fit the dose-response relationships.
MetS was associated with increased risk of CRC (n = 141; HR: 1.64, 95% CI: 1.15-2.33) after adjusting for confounding factors (age, sex, education level, family history of CRC, smoking index and alcohol index). Participants with hyperglycemia had a significantly higher risk of developing incident CRC (HR: 1.70; 95% CI: 1.19-2.43). The positive association between MetS and CRC was observed in males (HR: 1.76; 95% CI: 1.17-2.63), but not in females (HR: 1.24; 95% CI: 0.59-2.64). Furthermore, linear dose-response relationship was found between fasting plasma glucose (FPG) and CRC risk in males ( Poverall < 0.05, Pnon-linear = 0.35). When stratified by smoke and drink, MetS was found to increase the incidence of CRC only in the smoke (HR: 2.07, 95% CI: 1.35-3.18) and drink (HR: 2.93, 95% CI: 1.51-5.69) groups.
MetS was associated with a higher risk of CRC incidence. Hyperglycemia lended strong support to the role of MetS in new-onset CRC, especially in males. Other components of MetS were not found to be associated with increased risk of CRC.
基于金昌队列研究的数据,评估代谢综合征(MetS)及其组分与结直肠癌(CRC)发病之间的相关性。
这是一项大型前瞻性队列研究。2011 年至 2020 年期间,共纳入 43516 名来自金昌队列的个体进行本研究。采用 Cox 比例风险模型计算 MetS 与 CRC 之间的结直肠癌风险比(HR)及其 95%置信区间(CI)。采用带有四个结的限制性立方样条模型拟合剂量-反应关系。
在调整混杂因素(年龄、性别、教育程度、CRC 家族史、吸烟指数和饮酒指数)后,MetS 与 CRC 发病风险增加相关(n=141;HR:1.64,95%CI:1.15-2.33)。高血糖患者发生 CRC 的风险显著升高(HR:1.70;95%CI:1.19-2.43)。MetS 与 CRC 之间的阳性关联在男性中观察到(HR:1.76;95%CI:1.17-2.63),但在女性中未观察到(HR:1.24;95%CI:0.59-2.64)。此外,在男性中发现空腹血糖(FPG)与 CRC 风险之间存在线性剂量-反应关系(总体 P<0.05,P 非线性=0.35)。按吸烟和饮酒分层后,仅在吸烟(HR:2.07,95%CI:1.35-3.18)和饮酒(HR:2.93,95%CI:1.51-5.69)组中发现 MetS 会增加 CRC 的发病风险。
MetS 与 CRC 发病风险增加相关。高血糖为 MetS 在新诊断 CRC 中的作用提供了有力支持,尤其是在男性中。MetS 的其他组分与 CRC 风险增加无关。