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非诺贝特的定性作用及阿托伐他汀对伴有致密低密度脂蛋白的混合性高脂血症患者低密度脂蛋白谱的定量作用。

Qualitative effect of fenofibrate and quantitative effect of atorvastatin on LDL profile in combined hyperlipidemia with dense LDL.

作者信息

Winkler K, Weltzien P, Friedrich I, Schmitz H, Nickell H-H, Hauck P, Hoffmann M M, Baumstark M W, Wieland H, März W

机构信息

Department of Clinical Chemistry, University of Freiburg, Germany.

出版信息

Exp Clin Endocrinol Diabetes. 2004 May;112(5):241-7. doi: 10.1055/s-2004-817970.

Abstract

INTRODUCTION

The association of elevated plasma triglyceride concentrations, decreased HDL-cholesterol, and dense LDL (dLDL) is referred to as the atherogenic lipoprotein phenotype. dLDL particularly plays a role in the metabolic syndrome and type 2 diabetes and may be one of the factors responsible for the increased risk for coronary artery disease in these patients. The effect of fenofibrate and atorvastatin on the LDL subfraction profile in patients with combined hyperlipidemia and a preponderance of dLDL was studied in a sequential design.

METHODS

Six male patients with combined hyperlipidemia and dLDL received 160 mg/die supra-bioavailable fenofibrate. After a washout phase of 8 weeks all patients received 10 mg/die atorvastatin for another 8 weeks. At baseline, after fenofibrate, and after atorvastatin treatment LDL subfractions were analyzed by equilibrium density gradient ultracentrifugation.

RESULTS

Treatment with atorvastatin and fenofibrate reduced serum cholesterol by 30 % and 21 % (p = 0.046) (p-values for differences between treatment groups), triglycerides by 32 % and 45 %, LDL cholesterol by 28 % and 16 %, and increased HDL cholesterol by 3 % and 6 %, respectively. Atorvastatin and fenofibrate treatment resulted in the following changes of apoB and LDL subfractions: LDL-1 (1.019 - 1.031 kg/L) - 31 % and + 15 % (p = 0.028); LDL-2 (1.031 - 1.034 kg/L) - 14 % and + 57 % (p = 0.028); LDL-3 (1.034 - 1.037 kg/L) - 20 % and + 30 % (p = 0.028); LDL-4 (1.037 - 1.040 kg/L) - 25 % and - 6 %; LDL-5 (1.040 - 1.044 kg/L) - 29 % and - 38 %; and LDL-6 (1.044 - 1.063 kg/L) - 39 % and - 55 % (p = 0.028). As a consequence, fenofibrate reduced LDL density significantly (p = 0.028 versus atorvastatin).

CONCLUSIONS

Atorvastatin decreased all LDL-subfractions to a similar extent (quantitative effect) whereas fenofibrate reduced predominantly dLDL and changed the LDL profile towards medium dense LDL-particles (qualitative effect). Since medium dense LDL have a higher affinity to the LDL-receptor fenofibrate may have a higher antiatherogenic potential than assessed by the reduction of total LDL-cholesterol and triglycerides alone.

摘要

引言

血浆甘油三酯浓度升高、高密度脂蛋白胆固醇降低以及致密低密度脂蛋白(dLDL)的联合存在被称为致动脉粥样硬化脂蛋白表型。dLDL在代谢综合征和2型糖尿病中尤其起作用,可能是这些患者冠状动脉疾病风险增加的因素之一。本研究采用序贯设计,探讨非诺贝特和阿托伐他汀对合并高脂血症且以dLDL为主的患者低密度脂蛋白亚组分谱的影响。

方法

6例合并高脂血症和dLDL的男性患者接受160mg/日的超生物利用度非诺贝特治疗。经过8周的洗脱期后,所有患者再接受10mg/日的阿托伐他汀治疗8周。在基线、非诺贝特治疗后以及阿托伐他汀治疗后,通过平衡密度梯度超速离心法分析低密度脂蛋白亚组分。

结果

阿托伐他汀和非诺贝特治疗分别使血清胆固醇降低30%和21%(治疗组间差异的p值为0.046),甘油三酯降低32%和45%,低密度脂蛋白胆固醇降低28%和16%,高密度脂蛋白胆固醇分别升高3%和6%。阿托伐他汀和非诺贝特治疗导致载脂蛋白B和低密度脂蛋白亚组分发生以下变化:低密度脂蛋白-1(1.019 - 1.031kg/L)降低31%和升高15%(p = 0.028);低密度脂蛋白-2(1.031 - 1.034kg/L)降低14%和升高57%(p = 0.028);低密度脂蛋白-3(1.034 - 1.037kg/L)降低20%和升高30%(p = 0.028);低密度脂蛋白-4(1.037 - 1.040kg/L)降低25%和降低6%;低密度脂蛋白-5(1.040 - 1.044kg/L)降低29%和降低38%;低密度脂蛋白-6(1.044 - 1.063kg/L)降低39%和降低55%(p = 0.028)。因此,非诺贝特显著降低了低密度脂蛋白密度(与阿托伐他汀相比,p = 0.028)。

结论

阿托伐他汀在相似程度上降低了所有低密度脂蛋白亚组分(定量效应),而非诺贝特主要降低dLDL,并使低密度脂蛋白谱向中等密度的低密度脂蛋白颗粒转变(定性效应)。由于中等密度的低密度脂蛋白对低密度脂蛋白受体具有更高的亲和力,非诺贝特可能具有比仅通过降低总低密度脂蛋白胆固醇和甘油三酯所评估的更高的抗动脉粥样硬化潜力。

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