Tai E S, Fok A C, Chu R, Tan C E
Department of Endocrinology, Singapore General Hospital, Singapore.
Ann Acad Med Singap. 1999 Mar;28(2):209-13.
Hypercholesterolaemia is one of the major risk factors in the development of coronary artery disease. In recent years, many nonprescription treatments have become available for cholesterol lowering. Minolest is a product that contains guar gum and psyllium as the principal active ingredients. We conducted a randomised, placebo-controlled, double-blind, parallel-group study to assess the efficacy of Minolest as a lipid-lowering agent. Secondary aims included assessment of the effect on blood pressure and obesity. We also looked at the acceptability of the product and side effects associated with its ingestion. After a 4-week run-in period, 83 subjects were randomised to receive placebo or Minolest (16.5 g/day) for 3 months. Seven subjects defaulted follow up, 5 in the placebo group and 2 in the active treatment group. In addition, 9 subjects (5 on active treatment and 4 on placebo) had total cholesterol fall into the optimal range (< 5.2 mmol/l) during the run-in phase and were removed from the study. At baseline in the active treatment group, total cholesterol was 6.1 (5.43 to 8.06) mmol/l, triglyceride 1.54 (0.56 to 4.19) mmol/l, HDL cholesterol 1.32 +/- 0.43 mmol/l and LDL cholesterol 4.1 (3.10 to 6.27) mmol/l. In the placebo group, total cholesterol was 5.84 (5.32 to 8.38) mmol/l, triglyceride 1.47 (0.69 to 11.0) mmol/l, HDL cholesterol 1.15 +/- 0.33 mmol/l and LDL cholesterol 3.87 (2.46 to 5.14) mmol/l. The differences in the baseline characteristics were not statistically significant except the LDL-cholesterol. Minolest produced a 3.24% (SD = 7.85%, P = 0.020) decrease in total cholesterol and 5.45% decrease in LDL cholesterol (SD = 10.25%, P = 0.0034) but no significant difference in serum triglyceride, weight, body mass index or blood pressure. This was not seen in the placebo group. The percentage fall in LDL cholesterol increased to 7.16% and 7.37% in subjects who consumed at least 50% and 70% of the treatment respectively. There were few side effects. The authors conclude that this product has a small impact on the lipid profile and may be useful only in subjects with mild hypercholesterolaemia and a low risk of coronary artery disease.
高胆固醇血症是冠状动脉疾病发展的主要危险因素之一。近年来,出现了许多非处方降胆固醇治疗方法。Minolest是一种以瓜尔豆胶和车前子壳为主要活性成分的产品。我们进行了一项随机、安慰剂对照、双盲、平行组研究,以评估Minolest作为降脂药物的疗效。次要目标包括评估其对血压和肥胖的影响。我们还研究了该产品的可接受性以及摄入相关的副作用。在为期4周的导入期后,83名受试者被随机分为接受安慰剂或Minolest(16.5克/天)治疗3个月。7名受试者未完成随访,安慰剂组5名,活性治疗组2名。此外,9名受试者(5名接受活性治疗,4名接受安慰剂)在导入期总胆固醇降至最佳范围(<5.2毫摩尔/升),并被排除在研究之外。活性治疗组基线时,总胆固醇为6.1(5.43至8.06)毫摩尔/升,甘油三酯为1.54(0.56至4.19)毫摩尔/升,高密度脂蛋白胆固醇为1.32±0.43毫摩尔/升,低密度脂蛋白胆固醇为4.1(3.10至6.27)毫摩尔/升。安慰剂组中,总胆固醇为5.84(5.32至8.38)毫摩尔/升,甘油三酯为1.47(0.69至11.0)毫摩尔/升,高密度脂蛋白胆固醇为1.15±0.33毫摩尔/升,低密度脂蛋白胆固醇为3.87(2.46至5.14)毫摩尔/升。除低密度脂蛋白胆固醇外,基线特征的差异无统计学意义。Minolest使总胆固醇降低了3.24%(标准差=7.85%,P=0.020),低密度脂蛋白胆固醇降低了5.45%(标准差=10.25%,P=0.0034),但血清甘油三酯、体重、体重指数或血压无显著差异。安慰剂组未出现这种情况。分别至少服用50%和70%治疗药物的受试者中,低密度脂蛋白胆固醇的下降百分比分别增至7.16%和7.37%。副作用很少。作者得出结论,该产品对血脂谱影响较小,可能仅对轻度高胆固醇血症且冠状动脉疾病风险较低的受试者有用。