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本文引用的文献

1
Effects on Cell Proliferation, Activator Protein-1 and Genotoxicity by Fecal Water from Patients with Colorectal Adenomas.大肠腺瘤患者粪便水对细胞增殖、活化蛋白-1及遗传毒性的影响
Scand J Gastroenterol. 2003;38(5):549-555. doi: 10.1080/00365520310002913.
2
Primary biliary cirrhosis.原发性胆汁性肝硬化
Semin Immunopathol. 2009 Sep;31(3):283-307. doi: 10.1007/s00281-009-0164-5. Epub 2009 Jul 15.
3
Bile acids: regulation of apoptosis by ursodeoxycholic acid.胆酸:熊去氧胆酸对细胞凋亡的调控。
J Lipid Res. 2009 Sep;50(9):1721-34. doi: 10.1194/jlr.R900011-JLR200. Epub 2009 May 5.
4
Bile-acid-induced cell injury and protection.胆汁酸诱导的细胞损伤与保护
World J Gastroenterol. 2009 Apr 14;15(14):1677-89. doi: 10.3748/wjg.15.1677.
5
Lithogenesis and bile metabolism.结石形成与胆汁代谢
Surg Clin North Am. 2008 Dec;88(6):1175-94, vii. doi: 10.1016/j.suc.2008.07.009.
6
Association between fecal bile acids and colorectal cancer: a meta-analysis of observational studies.粪便胆汁酸与结直肠癌之间的关联:观察性研究的荟萃分析
Yonsei Med J. 2008 Oct 31;49(5):792-803. doi: 10.3349/ymj.2008.49.5.792.
7
Intestinal bile acid physiology and pathophysiology.肠道胆汁酸生理学与病理生理学。
World J Gastroenterol. 2008 Oct 7;14(37):5630-40. doi: 10.3748/wjg.14.5630.
8
Review article: current management of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis.综述文章:非酒精性脂肪性肝病和非酒精性脂肪性肝炎的当前管理
Aliment Pharmacol Ther. 2008 Jul;28(1):2-12. doi: 10.1111/j.1365-2036.2008.03710.x. Epub 2008 Apr 11.
9
Bile acids and apoptosis modulation: an emerging role in experimental Alzheimer's disease.胆汁酸与细胞凋亡调节:在实验性阿尔茨海默病中的新作用
Trends Mol Med. 2008 Feb;14(2):54-62. doi: 10.1016/j.molmed.2007.12.001. Epub 2008 Jan 22.
10
Molecular heterogeneity of colorectal cancer: Implications for cancer control.结直肠癌的分子异质性:对癌症控制的影响。
Surg Oncol. 2007 Dec;16 Suppl 1:S7-9. doi: 10.1016/j.suronc.2007.10.039. Epub 2007 Nov 26.

性别会影响熊去氧胆酸在结直肠腺瘤患者随机对照试验中的作用。

Gender modifies the effect of ursodeoxycholic acid in a randomized controlled trial in colorectal adenoma patients.

机构信息

Arizona Cancer Center, 1515 North Campbell Avenue, P.O. Box 245024, Tucson, AZ 85724, USA.

出版信息

Cancer Prev Res (Phila). 2009 Dec;2(12):1023-30. doi: 10.1158/1940-6207.CAPR-09-0234. Epub 2009 Dec 1.

DOI:10.1158/1940-6207.CAPR-09-0234
PMID:19952360
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4120755/
Abstract

PURPOSE

Ursodeoxycholic acid (UDCA) was one of the earliest agents investigated as a drug for colorectal cancer prevention. However, UDCA failed to show efficacy to prevent the development of colorectal adenomas in a large, phase III, randomized, placebo-controlled trial. We re-evaluated the effect of UDCA in men and women separately, based on sex-specific differences in bile acid metabolism and suspected variation in etiologic factors contributing to colorectal cancer risk.

EXPERIMENTAL DESIGN

We conducted a secondary analysis of the efficacy of UDCA to prevent colorectal adenoma in men (n = 804) and women (n = 388).

RESULTS

We found no reduction in risk of any metachronous adenoma with UDCA treatment in men or women. However, UDCA treatment significantly lowered the odds of advanced lesions [odds ratio (OR), 0.62; 95% confidence interval (CI), 0.43-0.89] in men, but not women. We also observed significantly higher odds of advanced lesions with UDCA treatment in women who were younger (age, <65 years; OR, 3.24; 95% CI, 1.10-9.56), obese (body mass index, > or = 30 kg/m(2); OR, 5.45; 95% CI, 1.42-20.9), or in the highest tertile of total dietary fat (> or = 56.2 g/day; OR, 3.48; 95% CI, 1.35-8.95). In a multivariate model, the interactive effect of fat intake accounted for the modulating effects of age and body mass index in women.

CONCLUSION

Our findings support the use of UDCA for preventing advanced colorectal adenomas in men. The increased odds of adenoma among women with high fat intake suggest a previously unrecognized harm that warrants further study, especially given the chronic exposure to UDCA in patients with primary biliary cirrhosis and the increasing investigational use of UDCA for several other conditions.

摘要

目的

熊去氧胆酸(UDCA)是最早被研究用于预防结直肠癌的药物之一。然而,在一项大型三期随机安慰剂对照试验中,UDCA未能显示出预防结直肠腺瘤发展的疗效。我们根据胆汁酸代谢的性别特异性差异以及对结直肠癌风险的潜在病因因素的变化,分别对男性和女性进行了 UDCA 疗效的重新评估。

实验设计

我们对 UDCA 预防男性(n=804)和女性(n=388)结直肠腺瘤的疗效进行了二次分析。

结果

我们没有发现 UDCA 治疗在男性或女性中降低任何异时性腺瘤的风险。然而,UDCA 治疗显著降低了男性高级病变的几率(比值比[OR],0.62;95%置信区间[CI],0.43-0.89),但对女性没有影响。我们还发现,在年龄较小(年龄<65 岁;OR,3.24;95%CI,1.10-9.56)、肥胖(体重指数≥30kg/m2;OR,5.45;95%CI,1.42-20.9)或总膳食脂肪最高三分位(≥56.2g/天;OR,3.48;95%CI,1.35-8.95)的女性中,UDCA 治疗后高级病变的几率显著更高。在多变量模型中,脂肪摄入量的交互作用解释了女性年龄和体重指数的调节作用。

结论

我们的研究结果支持 UDCA 用于预防男性结直肠高级腺瘤。在高脂肪摄入的女性中,腺瘤的发生率增加表明存在以前未被认识到的危害,这需要进一步研究,特别是考虑到原发性胆汁性肝硬化患者长期暴露于 UDCA 以及 UDCA 在其他几种情况下的研究性使用日益增加。