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本文引用的文献

1
C-reactive protein and colorectal adenoma in the CLUE II cohort.CLUE II队列中的C反应蛋白与结直肠腺瘤
Cancer Causes Control. 2008 Aug;19(6):559-67. doi: 10.1007/s10552-008-9117-x. Epub 2008 Jan 24.
2
Components of the metabolic syndrome and colorectal cancer risk; a prospective study.代谢综合征各组分与结直肠癌风险:一项前瞻性研究
Int J Obes (Lond). 2008 Feb;32(2):304-14. doi: 10.1038/sj.ijo.0803713. Epub 2007 Sep 18.
3
Is metabolic syndrome a risk factor for colorectal adenoma?代谢综合征是结肠直肠腺瘤的危险因素吗?
Cancer Epidemiol Biomarkers Prev. 2007 Aug;16(8):1543-6. doi: 10.1158/1055-9965.EPI-07-0199.
4
Serum C-peptide, IGFBP-1 and IGFBP-2 and risk of colon and rectal cancers in the European Prospective Investigation into Cancer and Nutrition.欧洲癌症与营养前瞻性调查中血清C肽、胰岛素样生长因子结合蛋白-1和胰岛素样生长因子结合蛋白-2与结肠癌和直肠癌风险的关系
Int J Cancer. 2007 Jul 15;121(2):368-76. doi: 10.1002/ijc.22697.
5
Plasma C-peptide, insulin-like growth factor-I, insulin-like growth factor binding proteins and risk of colorectal cancer in a nested case-control study: the Japan public health center-based prospective study.巢式病例对照研究中血浆C肽、胰岛素样生长因子-I、胰岛素样生长因子结合蛋白与结直肠癌风险:日本公共卫生中心前瞻性研究
Int J Cancer. 2007 May 1;120(9):2007-12. doi: 10.1002/ijc.22556.
6
Circulating insulin and c-peptide levels and risk of breast cancer among predominately premenopausal women.主要为绝经前女性的循环胰岛素和C肽水平与乳腺癌风险
Cancer Epidemiol Biomarkers Prev. 2007 Jan;16(1):161-4. doi: 10.1158/1055-9965.EPI-06-0693.
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Metabolic abnormalities and risk for colorectal cancer in the physicians' health study.医师健康研究中的代谢异常与结直肠癌风险
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The metabolic syndrome: A high-risk state for cancer?代谢综合征:癌症的高危状态?
Am J Pathol. 2006 Nov;169(5):1505-22. doi: 10.2353/ajpath.2006.051090.
9
A prospective study of anthropometric and clinical measurements associated with insulin resistance syndrome and colorectal cancer in male smokers.一项关于男性吸烟者中与胰岛素抵抗综合征及结直肠癌相关的人体测量和临床指标的前瞻性研究。
Am J Epidemiol. 2006 Oct 1;164(7):652-64. doi: 10.1093/aje/kwj253. Epub 2006 Jul 28.
10
The metabolic syndrome and risk of incident colorectal cancer.代谢综合征与结直肠癌发病风险
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代谢综合征组分与 CLUE II 队列中的结直肠腺瘤。

Metabolic syndrome components and colorectal adenoma in the CLUE II cohort.

机构信息

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD 21205, USA.

出版信息

Cancer Causes Control. 2010 Jan;21(1):1-10. doi: 10.1007/s10552-009-9428-6. Epub 2009 Sep 23.

DOI:10.1007/s10552-009-9428-6
PMID:19774471
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3010872/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSION

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.

摘要

背景

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。

方法

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)。

结果

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。

结论

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。