首页> 外文期刊>International journal of clinical pharmacology and therapeutics >Effects of fenofibrate and simvastatin on plasma sICAM-1 and MCP-1 concentrations in patients with hyperlipoproteinemia.
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Effects of fenofibrate and simvastatin on plasma sICAM-1 and MCP-1 concentrations in patients with hyperlipoproteinemia.

机译:非诺贝特和辛伐他汀对高脂蛋白血症患者血浆sICAM-1和MCP-1的影响。

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OBJECTIVE: The most important mechanism through which high plasma lipid levels trigger the formation of atherosclerotic lesions involves a change in the expression of adhesion molecules on endothelial and smooth muscle cells. The aim of this study was to evaluate an extralipid effect of fenofibrate and simvastatin by examination of MCP-1 and ICAM-1 plasma concentration after 1-month hypolipemic therapy as well as MCP-1 and ICAM-1 plasma concentration after 1-month therapy with low-fat diet alone. METHODS: Twenty patients with HLPIIb or HLPIIa, who did not respond to a low-fat diet, were treated with micronized fenofibrate or simvastatin, respectively, for 1 month. The control group included 18 normo-lipidemic, healthy age-matched participants; 10 patients with HLPIIa were effectively treated with a low-fat diet for 1 month. This group was compared to a control group of 10 healthy subjects. The plasma adhesion molecule levels were measured by an ELISA method before and after the treatment. To accuratelyevaluate the adhesion molecule levels, we excluded hyperlipidemic patients and control subjects with any inflammatory disease. RESULTS: sICAM-1 levels were significantly higher in HLPIIa and HLPIIb patients (331 +/- 19 ng/ml and 423 +/- 23 ng/ml, respectively) compared with the control group (236 +/- 12 mg/ml). MCP-1 levels were also significantly higher in HLPIIa and HLPIIb patients (170 +/- 9 pg/ml and 183 +/- 15 pg/ml, respectively) compared with the control group (100 +/- 4 pg/ml). Fenofibrate (200 mg daily) significantly decreased sICAM-1 (by 17%) and MCP-1 levels (by 12.5%). Simvastatin (20 mg daily) caused a significant decrease (by 10.5%) in sICAM-1 levels only. Restriction in dietary lipids resulted in a significant decrease in the levels of cholesterol (8%), LDL cholesterol (14.9%) and ApoB (12.7%), which was accompanied by a significant decrease in the levels of sICAM-1 (8.7%) and MCP-1 (16.1%). CONCLUSION: The results of this study suggest that high lipid levels are accompanied by increased levelsof sICAM-1 and MCP-1 and that hypolipidemic therapy only slightly decreases the levels of these molecules compared with plasma lipids. The hypolipidemic diet-related decrease in the levels of lipids, ICAM-1 and MCP-1 suggests that it is a drug-induced decrease in lipid levels but not a direct action of the drugs on endothelial cells, smooth muscle cells or macrophages that leads to a decrease in the levels of adhesion molecules.
机译:目的:高血脂水平触发动脉粥样硬化病变形成的最重要机制涉及内皮细胞和平滑肌细胞上粘附分子表达的变化。这项研究的目的是通过检查低血脂治疗1个月后的MCP-1和ICAM-1血浆浓度以及1个月治疗后的MCP-1和ICAM-1血浆浓度来评估非诺贝特和辛伐他汀的脂质外作用仅低脂饮食。方法:20例对低脂饮食无反应的HLPIIb或HLPIIa患者分别接受微粉非诺贝特或辛伐他汀治疗1个月。对照组包括18名血脂正常,年龄相匹配的健康参与者。低脂饮食有效治疗了10例HLPIIa患者1个月。将该组与10名健康受试者的对照组进行比较。在治疗之前和之后通过ELISA方法测量血浆粘附分子水平。为了准确评估粘附分子水平,我们排除了高脂血症患者和患有任何炎性疾病的对照组。结果:与对照组(236 +/- 12 mg / ml)相比,HLPIIa和HLPIIb患者的sICAM-1水平显着升高(分别为331 +/- 19 ng / ml和423 +/- 23 ng / ml)。 。与对照组(100 +/- 4 pg / ml)相比,HLPIIa和HLPIIb患者的MCP-1水平也显着更高(分别为170 +/- 9 pg / ml和183 +/- 15 pg / ml)。非诺贝特(每日200 mg)显着降低sICAM-1(降低17%)和MCP-1水平(降低12.5%)。辛伐他汀(每天20 mg)仅导致sICAM-1水平显着降低(降低10.5%)。限制饮食中的脂质导致胆固醇(8%),LDL胆固醇(14.9%)和ApoB(12.7%)的水平显着下降,同时sICAM-1(8.7%)的水平显着下降和MCP-1(16.1%)。结论:这项研究的结果表明,高血脂水平伴随着sICAM-1和MCP-1水平的升高,而降血脂治疗与血浆脂质相比仅略微降低了这些分子的水平。与低血脂饮食相关的脂质水平降低,ICAM-1和MCP-1表明这是药物诱导的脂质水平降低,但不是药物对内皮细胞,平滑肌细胞或巨噬细胞的直接作用降低粘附分子的水平。

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