Section of Nutrition and Metabolism, International Agency for Research on Cancer, Lyon, France.
Unit of Nutrition and Cancer, Cancer Epidemiology Research Programme, Catalan Institute of Oncology, Bellvitge Biomedical Research Institute (IDIBELL), Barcelona, Spain.
Int J Cancer. 2018 Oct 1;143(7):1620-1631. doi: 10.1002/ijc.31563. Epub 2018 Jun 11.
Polyphenols have been shown to exert biological activity in experimental models of colon cancer; however, human data linking specific polyphenols to colon cancer is limited. We assessed the relationship between pre-diagnostic plasma polyphenols and colon cancer risk in a case-control study nested within the European Prospective Investigation into Cancer and Nutrition study. Using high pressure liquid chromatography coupled to tandem mass spectrometry, we measured concentrations of 35 polyphenols in plasma from 809 incident colon cancer cases and 809 matched controls. We used multivariable adjusted conditional logistic regression models that included established colon cancer risk factors. The false discovery rate (q ) was computed to control for multiple comparisons. All statistical tests were two-sided. After false discovery rate correction and in continuous log -transformed multivariable models, equol (odds ratio [OR] per log -value, 0.86, 95% confidence interval [95% CI] = 0.79-0.93; q = 0.01) and homovanillic acid (OR per log -value, 1.46, 95% CI = 1.16-1.84; q = 0.02) were associated with colon cancer risk. Comparing extreme fifths, equol concentrations were inversely associated with colon cancer risk (OR = 0.61, 95% CI = 0.41-0.91, p = 0.003), while homovanillic acid concentrations were positively associated with colon cancer development (OR = 1.72, 95% CI = 1.17-2.53, p < 0.0001). No heterogeneity for these associations was observed by sex and across other colon cancer risk factors. The remaining polyphenols were not associated with colon cancer risk. Higher equol concentrations were associated with lower risk, and higher homovanillic acid concentrations were associated with greater risk of colon cancer. These findings support a potential role for specific polyphenols in colon tumorigenesis.
多酚已被证明在结肠癌的实验模型中具有生物活性;然而,将特定多酚与结肠癌联系起来的人体数据有限。我们在欧洲癌症前瞻性调查和营养研究中嵌套的病例对照研究中评估了预诊断血浆多酚与结肠癌风险之间的关系。使用高压液相色谱-串联质谱法,我们测量了 809 例结肠癌病例和 809 例匹配对照的血浆中 35 种多酚的浓度。我们使用包括已确立的结肠癌危险因素在内的多变量调整条件逻辑回归模型。错误发现率 (q) 用于控制多重比较。所有统计检验均为双侧。在经过错误发现率校正和连续对数变换的多变量模型中,马尿酸(每对数的比值 [OR],0.86,95%置信区间 [95%CI] = 0.79-0.93;q = 0.01)和高香草酸(每对数的比值 [OR],1.46,95%CI = 1.16-1.84;q = 0.02)与结肠癌风险相关。比较极端五分位数,马尿酸浓度与结肠癌风险呈负相关(比值比 [OR],0.61,95%CI = 0.41-0.91,p = 0.003),而高香草酸浓度与结肠癌发展呈正相关(比值比 [OR],1.72,95%CI = 1.17-2.53,p < 0.0001)。这些关联在性别和其他结肠癌危险因素方面没有异质性。其余的多酚与结肠癌风险无关。较高的马尿酸浓度与较低的风险相关,而较高的高香草酸浓度与较高的结肠癌风险相关。这些发现支持特定多酚在结肠癌发生中的潜在作用。