Yong Q W, Thavintharan S, Cheng A, Chew L S
Department of Cardiology, Tan Tock Seng Hospital, Singapore.
Ann Acad Med Singap. 1999 Nov;28(6):778-82.
Non-diabetic males, particularly those with very low levels of high density lipoprotein (HDL) type cholesterol and high levels of very low density type lipoprotein (VLDL), are associated with insulin resistance and decreased insulin sensitivity. The evidence that elevation of HDL cholesterol and diminution of triglycerides with drugs, with improvement in insulin sensitivity is still lacking. In the treatment of the dyslipidaemic syndromes with hypolipidaemic drugs, the associated metabolic abnormality of insulin resistance/sensitivity has to be addressed. We investigated the degree of decreased insulin sensitivity in 23 patients with low HDL and/or raised triglycerides by measuring the fasting, first and second hour insulin levels during an oral glucose tolerance test (OGTT) and repeated the measurements after a 6-month course of fenofibrate. The insulin levels were correlated with the OGTT, blood pressure, total cholesterol, HDL cholesterol, LDL cholesterol, and triglycerides measured before and at the end of the trial. The serum insulin at the second hour of the OGTT fell from 100.79 +/- 42.79 mU/l to 54.56 +/- 25.43 mU/l (P < 0.0005) even though there was no change in the blood glucose level at this point. Our study shows that fenofibrate (Lipanthyl) 300 mg daily significantly raises the pretreatment low HDL cholesterol (from 0.64 +/- 0.1 mmol/l to 0.99 +/- 0.2 mmol/l) as well as lowers the triglyceride level (from 2.17 +/- 1.1 mmol/l to 1.43 +/- 0.64 mmol/l) in patients with low HDL/dyslipidaemic syndrome. The data also support the conclusion that treatment with fenofibrate increases insulin sensitivity as measured by the corresponding insulin levels of the OGTT in the study subjects who presented with very low HDL cholesterol level. There was also a decrease in blood pressure readings in our study subjects. Throughout the trial, there was no significant change in body weight or exercise level in the subjects studied.
非糖尿病男性,尤其是那些高密度脂蛋白(HDL)胆固醇水平极低且极低密度脂蛋白(VLDL)水平高的男性,与胰岛素抵抗及胰岛素敏感性降低有关。目前仍缺乏证据表明通过药物升高HDL胆固醇并降低甘油三酯可改善胰岛素敏感性。在使用降血脂药物治疗血脂异常综合征时,必须解决与之相关的胰岛素抵抗/敏感性代谢异常问题。我们通过测量口服葡萄糖耐量试验(OGTT)期间的空腹、第一小时和第二小时胰岛素水平,研究了23例HDL低和/或甘油三酯升高患者胰岛素敏感性降低的程度,并在服用非诺贝特6个月疗程后重复测量。胰岛素水平与试验前及试验结束时测量的OGTT、血压、总胆固醇、HDL胆固醇、LDL胆固醇和甘油三酯相关。尽管此时血糖水平没有变化,但OGTT第二小时的血清胰岛素从100.79±42.79 mU/l降至54.56±25.43 mU/l(P<0.0005)。我们的研究表明,对于HDL低/血脂异常综合征患者,每日300毫克非诺贝特(力平之)可显著提高治疗前较低的HDL胆固醇水平(从0.64±0.1 mmol/l升至0.99±0.2 mmol/l),同时降低甘油三酯水平(从2.17±1.1 mmol/l降至1.43±0.64 mmol/l)。数据还支持以下结论:在HDL胆固醇水平极低的研究对象中,用非诺贝特治疗可提高胰岛素敏感性,这通过OGTT相应的胰岛素水平来衡量。我们的研究对象血压读数也有所下降。在整个试验过程中,研究对象的体重或运动水平没有显著变化。