海报会议1:基础科学:生物标志物,成像和脂质

Demirtas Hakan, U. Dilek, Kozdag Guliz, Ertas Gokhan, T. Şahin, O. Gokhan, Ulaş Bildirici, P. Rask, M. Dreifaldt, A. Hurtig-Wennlof, M. Pytliak, V. Vargová, V. Mechírová, M. Felsoci
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At entry and end of the study; blood and urine samples were collected fort he biochemical analyses and brachial artery reactivity and carotis intima-media thicknes were measured using high resolution ultrasonography. Results: A total of 52 patients completed the study. With both drugs; treatment goals of total cholesterol, LDL cholesterol, HDL cholesterol and nonHDL cholesterol was reached similarly. CRP reductions were significant in both groups (p1⁄40.041 vs p1⁄40.003) By fenofibrate; while levels of fibrinogen, uric acid and inslin were significantly declined and HOMA index was reduced (p1⁄4 0.003, p<0,001, ; p1⁄40.001, p1⁄4 0.002 respectively), a significant rise in the homocystein levels was observed (p1⁄40.015). In each groups; significant (p1⁄40,002 for atorvastatin and p1⁄40.022 for fenofibrate) and similar improvements occured on flow-mediated dilation of the brachial artery. 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引用次数: 0

摘要

P115阿托伐他汀和微细非诺贝特对代谢综合征患者内皮功能的影响:比较研究MD Demir Hakan, MD Ural Dilek, MD Kozdag Guliz, MD Ertas Gokhan, MD Tayfun Sahin, MD Oner Gokhan, MD Ulas Bildirici目的:比较阿托伐他汀10 mg/d和非诺贝特200 mg/d对代谢综合征患者传统和非传统风险及内皮功能的影响。材料与方法:对65例连续无冠状动脉的患者进行研究。患者被随机分配到阿托伐他汀10毫克/天或非诺贝特200毫克/天。在研究开始和结束时;采用高分辨率超声检查肱动脉反应性和颈动脉内膜-中膜厚度,采集血、尿样本进行生化分析。结果:共有52例患者完成了研究。两种药物;总胆固醇、低密度脂蛋白胆固醇、高密度脂蛋白胆固醇和非高密度脂蛋白胆固醇的治疗目标相似。两组CRP均显著降低(p1 / 40.041 vs p1 / 40.003);纤维蛋白原、尿酸、胰岛素水平显著下降,HOMA指数降低(p1 / 4 0.003, p< 0.001,;P1 / 40.001, P1 / 4 0.002),同型半胱氨酸水平显著升高(P1 / 40.015)。在每一组中;阿托伐他汀组为p1⁄40,002,非诺贝特组为p1⁄40.022),血流介导的肱动脉扩张出现了显著改善。结论:阿托伐他汀10mg /天或非诺贝特颗粒化200mg /天治疗6个月对代谢综合征内皮血管舒缩功能有相似的有益效果,但副作用较小。两者都能显著且相似地降低CRP水平。虽然阿托伐他汀对低密度脂蛋白胆固醇和总胆固醇更有效,但非诺贝特对胰岛素抵抗和内皮功能障碍的血清标志物更有效。这两种药物都是代谢综合征的良好治疗选择,但在选择更合适的药物时,还应考虑患者的脂质状况和动脉粥样硬化的其他标志物。联合治疗必须牢记并密切监测副作用。
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Poster Session I: Basic science: biomarkers, imaging and lipids
P115 The effects of atorvastatin and micronized fenofibrate on endothelial functions in metabolic syndrome patients: comparative study MD Demir Hakan, MD Ural Dilek, MD Kozdag Guliz, MD Ertas Gokhan, MD Tayfun Sahin, MD Oner Gokhan, MD Ulas Bildirici Department of Cardiology, Kocaeli, Turkey Topic: Obesity Objective:To compare the effects of atorvastatin 10 mg/day andmicronized fenofibrate 200 mg/ day on traditional and non-traditional risk and endothelial functions in patients with metabolic syndrome. Materials and Methods: Sixty-five consecutive patients who were free of coronary artery were studied. Patients were randomized to atorvastatin 10 mg/da yor micronized fenofibrate 200 mg/ day. At entry and end of the study; blood and urine samples were collected fort he biochemical analyses and brachial artery reactivity and carotis intima-media thicknes were measured using high resolution ultrasonography. Results: A total of 52 patients completed the study. With both drugs; treatment goals of total cholesterol, LDL cholesterol, HDL cholesterol and nonHDL cholesterol was reached similarly. CRP reductions were significant in both groups (p1⁄40.041 vs p1⁄40.003) By fenofibrate; while levels of fibrinogen, uric acid and inslin were significantly declined and HOMA index was reduced (p1⁄4 0.003, p<0,001, ; p1⁄40.001, p1⁄4 0.002 respectively), a significant rise in the homocystein levels was observed (p1⁄40.015). In each groups; significant (p1⁄40,002 for atorvastatin and p1⁄40.022 for fenofibrate) and similar improvements occured on flow-mediated dilation of the brachial artery. Conclusion: Treatment with atorvastatin 10 mg/day or micronized fenofibrate 200 mg/day during six months have similar benefical effects on endothelial vasomotor functions inmetabolic syndrome with desirable side effects. Both reduce CRP levels significantly and similarly. While atorvastatin is more effective on LDL cholesterol and total cholesterol, fenofibrate is more effective on inslin resistance and the serum markers of endothelial dysfunction. Both drugs are good treatment options in metabolic syndrome, however lipid status of the patient and the other markers of atherosclerosis should also be considered while selecting the more suitable agent. Combination therapy must be kept in mind with close monitoring of the side effects.
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