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聚多卡醇和洛伐他汀对2型糖尿病伴血脂异常患者血脂谱及脂质过氧化的影响。

Effects of policosanol and lovastatin on lipid profile and lipid peroxidation in patients with dyslipidemia associated with type 2 diabetes mellitus.

作者信息

Castaño G, Menéndez R, Más R, Amor A, Fernández J L, González R L, Lezcay M, Alvarez E

机构信息

Medical Surgical Research Center, Havana City, Cuba.

出版信息

Int J Clin Pharmacol Res. 2002;22(3-4):89-99.

Abstract

In this pilot, randomized, double-blind study, we compared the effects of policosanol and lovastatin on lipid profile and lipid peroxidation in patients with dyslipidemia and type 2 diabetes mellitus. After 4 weeks on a cholesterol-lowering diet, 36 patients were randomized to policosanol (10 mg/day) or lovastatin (20 mg/day) tablets o.i.d. for 8 weeks. Policosanol significantly (p < 0.001) lowered serum low-density lipoprotein-cholesterol (LDL-C) (29.9%), total cholesterol (21.1%), triglycerides (13.6%) and the LDL-C/high-density lipoprotein-cholesterol (HDL-C) (36.7%) and total cholesterol/HDL-C (28.9%) ratios and significantly (p < 0.01) increased HDL-C (12.5%). Lovastatin significantly (p < 0.001) lowered LDL-C (25%), total cholesterol (18%), triglycerides (10.9%) and the LDL-C/HDL-C (30.4%) and total cholesterol/HDL-C ratios (23.9%) and significantly (p < 0.01) raised HDL-C (8.3%). Policosanol was more effective (p < 0.05) than lovastatin in reducing both ratios and in increasing (p < 0.05) HDL-C. Policosanol, but not lovastatin, significantly raised the lag time (20.9%) of Cu+2-induced LDL peroxidation and total plasma antioxidant activity (24.2%) (p < 0.05). Both policosanol and lovastatin significantly decreased the propagation rate (41.9% and 41.6% respectively, p < 0.001), maximal diene production (8.3% and 5.7%) and plasma levels of thiobarbituric acid reactive substances (9.7% and 11.5%, p < 0.001). Both treatments were well tolerated. Only one patient in the lovastatin group withdrew from the trial due to adverse events. In conclusion, policosanol and lovastatin administered short term to patients with dyslipidemia secondary to type 2 diabetes were effective in lowering cholesterol and in inhibiting the extent of lipid peroxidation. Policosanol (10 mg/day) was slightly more effective than lovastatin (20 mg/day) in reducing the LDL-C/HDL-C and total cholesterol/HDL-C ratios, in increasing HDL-C levels and in preventing LDL oxidation. Nevertheless, since this was a pilot study, further clinical studies performed in larger sample sizes of diabetic patients are needed for definitive conclusions.

摘要

在这项先导性、随机、双盲研究中,我们比较了多廿烷醇和洛伐他汀对血脂异常合并2型糖尿病患者血脂谱及脂质过氧化的影响。在进行4周的降胆固醇饮食后,36例患者被随机分为两组,分别服用多廿烷醇(10毫克/天)或洛伐他汀(20毫克/天)片剂,每日3次,持续8周。多廿烷醇显著(p<0.001)降低血清低密度脂蛋白胆固醇(LDL-C)(29.9%)、总胆固醇(21.1%)、甘油三酯(13.6%)以及LDL-C/高密度脂蛋白胆固醇(HDL-C)(36.7%)和总胆固醇/HDL-C(28.9%)比值,并显著(p<0.01)升高HDL-C(12.5%)。洛伐他汀显著(p<0.001)降低LDL-C(25%)、总胆固醇(18%)、甘油三酯(10.9%)以及LDL-C/HDL-C(30.4%)和总胆固醇/HDL-C比值(23.9%),并显著(p<0.01)升高HDL-C(8.3%)。在降低两个比值以及升高(p<0.05)HDL-C方面,多廿烷醇比洛伐他汀更有效(p<0.05)。多廿烷醇能显著(p<0.05)延长Cu+2诱导的LDL过氧化的延迟时间(20.9%)和提高血浆总抗氧化活性(24.2%),而洛伐他汀无此作用。多廿烷醇和洛伐他汀均显著降低脂质过氧化的传播速率(分别为41.9%和41.6%,p<0.001)、最大二烯生成量(8.3%和5.7%)以及血浆中硫代巴比妥酸反应性物质水平(9.7%和11.5%,p<0.001)。两种治疗的耐受性均良好。洛伐他汀组仅有1例患者因不良事件退出试验。总之,短期给予2型糖尿病继发血脂异常患者多廿烷醇和洛伐他汀可有效降低胆固醇并抑制脂质过氧化程度。在降低LDL-C/HDL-C和总胆固醇/HDL-C比值、升高HDL-C水平以及预防LDL氧化方面,多廿烷醇(10毫克/天)比洛伐他汀(20毫克/天)稍有效。然而,由于这是一项先导性研究,需要在更大样本量的糖尿病患者中进行进一步的临床研究才能得出确切结论。

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