Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.
Cancer Causes Control. 2010 Jan;21(1):1-10. doi: 10.1007/s10552-009-9428-6. Epub 2009 Sep 23.
Metabolic syndrome components have been associated with colorectal cancer in several studies; however, evidence for colorectal adenomas is limited. Thus, we evaluated the association between markers of the metabolic syndrome with colorectal adenoma development in a nested case-control study.
Colorectal adenoma cases (n = 132) and matched controls, who had a negative sigmoidoscopy or a colonoscopy (n = 260), were identified between baseline in 1989 and 2000 among participants in the CLUE II cohort of Washington County, Maryland. Concentrations of C-peptide, insulin-like growth factor binding protein-1, glycosylated hemoglobin, total cholesterol, high-density lipoprotein cholesterol, and triglycerides were measured in baseline blood specimens. Body mass index was calculated using baseline height and weight. Use of medications to treat diabetes mellitus was self-reported at baseline. Blood pressure was measured at baseline. Distributional cutpoints of the latter markers were used to define the metabolic syndrome components (hyperinsulinemia, hyperglycemia, obesity, dyslipidemia, and hypertension) present at baseline.
No statistically significant associations with adenomas were observed for the markers of the metabolic syndrome, with the exception of a strong positive association for use of diabetes medications (OR, 8.00; 95% CI, 1.70-37.67), albeit based on small numbers.
Our findings do not support that components of the metabolic syndrome influence risk of colorectal adenomas, except possibly for severe diabetes mellitus warranting medical treatment.
几项研究表明,代谢综合征的成分与结直肠癌有关;然而,关于结直肠腺瘤的证据有限。因此,我们评估了代谢综合征的标志物与马里兰州华盛顿县 CLUE II 队列研究中参与者基线时(1989 年至 2000 年)结肠镜或乙状结肠镜检查阴性的结直肠腺瘤发展之间的关联。
在马里兰州华盛顿县 CLUE II 队列的参与者中,在基线(1989 年至 2000 年)时,从结直肠腺瘤病例(n = 132)和阴性乙状结肠镜或结肠镜检查的匹配对照(n = 260)中确定结直肠腺瘤病例和匹配对照。基线血液标本中测量 C 肽、胰岛素样生长因子结合蛋白-1、糖化血红蛋白、总胆固醇、高密度脂蛋白胆固醇和甘油三酯的浓度。基线时使用身高和体重计算体重指数。基线时自我报告治疗糖尿病的药物使用情况。基线时测量血压。使用这些标志物的分布截断值来定义基线时存在的代谢综合征成分(高胰岛素血症、高血糖、肥胖、血脂异常和高血压)。
除了糖尿病药物治疗(比值比,8.00;95%置信区间,1.70-37.67)具有很强的正相关性外,代谢综合征的标志物与腺瘤之间没有观察到统计学上的显著相关性,尽管数量较小。
我们的研究结果不支持代谢综合征的成分会影响结直肠腺瘤的风险,除了可能需要药物治疗的严重糖尿病。