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胆汁酸排泄与动脉粥样硬化性冠状动脉疾病的关系。

The association of bile acid excretion and atherosclerotic coronary artery disease.

机构信息

Department of Internal Medicine "C", Tel Aviv Sourasky Medical Center, 6 Weizman Street, Tel Aviv 64239, Israel.

出版信息

Therap Adv Gastroenterol. 2011 Mar;4(2):95-101. doi: 10.1177/1756283X10388682.

Abstract

BACKGROUND

Excess cholesterol is usually eliminated from the body by conversion to bile acids excreted in feces as bile salts. The excretion of large amounts of bile protects against atherosclerosis, while diminished excretion may lead to coronary artery disease (CAD).

OBJECTIVE

To investigate a relationship between CAD and bile acid excretion.

METHODS

Bile acid excretion was compared between 36 patients with proven CAD and 37 CAD-free individuals (controls). The groups were comparable for demographics and selected risk factors. All subjects received a 4-day standard diet that included ∼500 mg of cholesterol. Fecal bile acids from 24-hour stool collections were measured by gas liquid chromatography.

RESULTS

CAD patients excreted lower amounts of total bile acids (358 ± 156 mg) than controls (617 ± 293 mg; p < 0.01) and less deoxycholic acid (188.29 ± 98.12 mg versus 325.96 ± 198.57 mg; p < 0.0001) and less lithocholic acid (115.43 ± 71.89 mg versus 197.27 ± 126.87 mg; p < 0.01). Advanced age, male gender, left ventricular ejection fraction and total bile acid levels were significant independent factors that predicted CAD (p < 0.05). Mortality, CAD and cerebrovascular accident development rates were significantly lower for the controls at the 13-year follow up.

CONCLUSION

CAD patients have significantly decreased bile acid excretion levels than non-CAD patients. An impaired ability to excrete cholesterol may be an additional risk factor for CAD development.

摘要

背景

过量的胆固醇通常通过转化为胆盐从粪便中排泄到胆汁中而从体内排出。大量胆汁的排泄可预防动脉粥样硬化,而排泄减少则可能导致冠心病(CAD)。

目的

研究 CAD 与胆汁酸排泄之间的关系。

方法

比较了 36 例经证实的 CAD 患者和 37 例 CAD 患者(对照组)的胆汁酸排泄情况。两组在人口统计学和选定的危险因素方面具有可比性。所有患者均接受为期 4 天的标准饮食,其中包括约 500mg 的胆固醇。通过气相色谱法测量 24 小时粪便收集的粪便胆汁酸。

结果

CAD 患者的总胆汁酸排泄量(358±156mg)低于对照组(617±293mg;p<0.01),脱氧胆酸(188.29±98.12mg 对 325.96±198.57mg;p<0.0001)和石胆酸(115.43±71.89mg 对 197.27±126.87mg;p<0.01)的排泄量也较少。年龄较大、男性、左心室射血分数和总胆汁酸水平是预测 CAD 的显著独立因素(p<0.05)。在 13 年的随访中,对照组的死亡率、CAD 和脑血管意外发生率明显较低。

结论

CAD 患者的胆汁酸排泄水平明显低于非 CAD 患者。胆固醇排泄能力受损可能是 CAD 发展的另一个危险因素。

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本文引用的文献

1
The metabolism of plant sterols is disturbed in postmenopausal women with coronary artery disease.
Metabolism. 2009 Mar;58(3):401-7. doi: 10.1016/j.metabol.2008.10.015.
5
Inhibition of ileal bile acid transport and reduced atherosclerosis in apoE-/- mice by SC-435.
J Lipid Res. 2003 Sep;44(9):1614-21. doi: 10.1194/jlr.M200469-JLR200. Epub 2003 Jun 16.
6
Increased fecal bile acid excretion in transgenic mice with elevated expression of human phospholipid transfer protein.
Arterioscler Thromb Vasc Biol. 2003 May 1;23(5):892-7. doi: 10.1161/01.ATV.0000067702.22390.20. Epub 2003 Mar 20.
7
Serum plant sterols as a potential risk factor for coronary heart disease.
Metabolism. 2002 Dec;51(12):1519-21. doi: 10.1053/meta.2002.36298.
8
Cholesterol absorption, synthesis, and fecal output in postmenopausal women with and without coronary artery disease.
Arterioscler Thromb Vasc Biol. 2001 Oct;21(10):1650-5. doi: 10.1161/hq1001.097019.
9
New molecular targets for cholesterol-lowering therapy.
J Pharmacol Exp Ther. 2000 May;293(2):315-20.

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