German Cancer Research Center (DKFZ), Division of Cancer Epidemiology, Heidelberg, Germany.
International Agency for Research on Cancer, Nutritional Epidemiology Group.
J Natl Cancer Inst. 2020 May 1;112(5):516-524. doi: 10.1093/jnci/djz166.
Bile acids have been proposed to promote colon carcinogenesis. However, there are limited prospective data on circulating bile acid levels and colon cancer risk in humans.
Associations between prediagnostic plasma levels of 17 primary, secondary, and tertiary bile acid metabolites (conjugated and unconjugated) and colon cancer risk were evaluated in a nested case-control study within the European Prospective Investigation into Cancer and Nutrition (EPIC) cohort. Bile acid levels were quantified by tandem mass spectrometry in samples from 569 incident colon cancer cases and 569 matched controls. Multivariable logistic regression analyses were used to estimate odds ratios (ORs) for colon cancer risk across quartiles of bile acid concentrations.
Positive associations were observed between colon cancer risk and plasma levels of seven conjugated bile acid metabolites: the primary bile acids glycocholic acid (ORquartile 4 vs quartile 1= 2.22, 95% confidence interval [CI] = 1.52 to 3.26), taurocholic acid (OR = 1.78, 95% CI = 1.23 to 2.58), glycochenodeoxycholic acid (OR = 1.68, 95% CI = 1.13 to 2.48), taurochenodeoxycholic acid (OR = 1.62, 95% CI = 1.11 to 2.36), and glycohyocholic acid (OR = 1.65, 95% CI = 1.13 to 2.40), and the secondary bile acids glycodeoxycholic acid (OR = 1.68, 95% CI = 1.12 to 2.54) and taurodeoxycholic acid (OR = 1.54, 95% CI = 1.02 to 2.31). By contrast, unconjugated bile acids and tertiary bile acids were not associated with risk.
This prospective study showed that prediagnostic levels of certain conjugated primary and secondary bile acids were positively associated with risk of colon cancer. Our findings support experimental data to suggest that a high bile acid load is colon cancer promotive.
胆汁酸被认为可以促进结肠癌的发生。然而,目前关于人类循环胆汁酸水平与结肠癌风险的前瞻性数据有限。
在欧洲癌症前瞻性调查和营养(EPIC)队列中进行的一项巢式病例对照研究中,评估了 569 例结肠癌病例和 569 例匹配对照的诊断前血浆中 17 种主要、次要和三级胆汁酸代谢物(结合型和非结合型)的水平与结肠癌风险之间的关联。采用串联质谱法定量测定胆汁酸水平。采用多变量逻辑回归分析评估胆汁酸浓度四分位区间与结肠癌风险的比值比(OR)。
观察到结肠癌风险与七种结合型胆汁酸代谢物的血浆水平呈正相关:初级胆汁酸甘氨胆酸(ORquartile 4 vs quartile 1=2.22,95%置信区间[CI] = 1.52 至 3.26)、牛磺胆酸(OR=1.78,95% CI = 1.23 至 2.58)、甘氨鹅脱氧胆酸(OR=1.68,95% CI = 1.13 至 2.48)、牛磺鹅脱氧胆酸(OR=1.62,95% CI = 1.11 至 2.36)和甘氨胆酸(OR=1.65,95% CI = 1.13 至 2.40),以及次级胆汁酸甘脱氧胆酸(OR=1.68,95% CI = 1.12 至 2.54)和牛磺脱氧胆酸(OR=1.54,95% CI = 1.02 至 2.31)。相比之下,非结合胆汁酸和三级胆汁酸与风险无关。
这项前瞻性研究表明,某些结合型初级和次级胆汁酸的诊断前水平与结肠癌风险呈正相关。我们的研究结果支持实验数据表明,高胆汁酸负荷可促进结肠癌的发生。