Division of Endocrinology, Metabolism, and Lipid Research, Department of Medicine, Washington University School of Medicine, St. Louis, MO 63110, USA.
Circulation. 2011 Aug 2;124(5):596-601. doi: 10.1161/CIRCULATIONAHA.110.006692. Epub 2011 Jul 18.
Both ezetimibe and phytosterols inhibit cholesterol absorption. We tested the hypothesis that the combination of ezetimibe and phytosterols is more effective than ezetimibe alone in altering cholesterol metabolism.
Twenty-one mildly hypercholesterolemic subjects completed a randomized, double-blind, placebo-controlled, triple-crossover study. Each subject received a phytosterol-controlled diet plus (1) ezetimibe placebo+phytosterol placebo, (2) 10 mg/d ezetimibe+phytosterol placebo, and (3) 10 mg/d ezetimibe+2.5 g phytosterols for 3 weeks each. All meals were prepared in a metabolic kitchen. Primary outcomes were intestinal cholesterol absorption, fecal cholesterol excretion, and low-density lipoprotein cholesterol levels. The combined treatment resulted in significantly lower intestinal cholesterol absorption (598 mg/d; 95% confidence interval [CI], 368 to 828) relative to control (2161 mg/d; 95% CI, 1112 to 3209) and ezetimibe alone (1054 mg/d; 95% CI, 546 to 1561; both P<0.0001). Fecal cholesterol excretion was significantly greater (P<0.0001) with combined treatment (962 mg/d; 95% CI, 757 to 1168) relative to control (505 mg/d; 95% CI, 386 to 625) and ezetimibe alone (794 mg/d; 95% CI, 615 to 973). Plasma low-density lipoprotein cholesterol values during treatment with control, ezetimibe alone, and ezetimibe+phytosterols averaged 129 mg/dL (95% CI, 116 to 142), 108 mg/dL (95% CI, 97 to 119), and 101 mg/dL (95% CI, 90 to 112; (P<0.0001 relative to control).
The addition of phytosterols to ezetimibe significantly enhanced the effects of ezetimibe on whole-body cholesterol metabolism and plasma low-density lipoprotein cholesterol. The large cumulative action of combined dietary and pharmacological treatment on cholesterol metabolism emphasizes the potential importance of dietary phytosterols as adjunctive therapy for the treatment of hypercholesterolemia.
URL: http://www.clinicaltrials.gov. Unique identifier: NCT00863265.
依折麦布和植物固醇都能抑制胆固醇吸收。我们验证了这样一个假设,即依折麦布与植物固醇联合应用比单用依折麦布更能有效改变胆固醇代谢。
21 名轻度高胆固醇血症患者完成了一项随机、双盲、安慰剂对照、三交叉研究。每位患者接受植物固醇控制饮食加(1)依折麦布安慰剂+植物固醇安慰剂,(2)10 mg/d 依折麦布+植物固醇安慰剂,和(3)10 mg/d 依折麦布+2.5 g 植物固醇,每种方案治疗 3 周。所有膳食均在代谢厨房准备。主要转归为肠道胆固醇吸收率、粪便胆固醇排泄量和低密度脂蛋白胆固醇水平。联合治疗组肠道胆固醇吸收率显著低于对照组(598 mg/d;95%可信区间[CI],368 至 828)和单用依折麦布组(1054 mg/d;95%CI,546 至 1561;均 P<0.0001)。联合治疗组粪便胆固醇排泄量显著增加(P<0.0001),显著高于对照组(505 mg/d;95%CI,386 至 625)和单用依折麦布组(794 mg/d;95%CI,615 至 973)。用对照组、单用依折麦布和依折麦布+植物固醇治疗时,患者的平均低密度脂蛋白胆固醇值分别为 129 mg/dL(95%CI,116 至 142)、108 mg/dL(95%CI,97 至 119)和 101 mg/dL(95%CI,90 至 112;与对照组相比,均 P<0.0001)。
植物固醇与依折麦布联合应用可显著增强依折麦布对全身胆固醇代谢和血浆低密度脂蛋白胆固醇的作用。饮食和药物联合治疗对胆固醇代谢的累积作用很大,这突出表明饮食中的植物固醇作为高胆固醇血症辅助治疗的潜在重要性。