Rizos Christos V, Kostapanos Michael S, Rizos Evangelos C, Tselepis Alexandros D, Elisaf Moses S
Department of Internal Medicine, Medical School, University of Ioannina, Ioannina, Greece.
Laboratory of Biochemistry, School of Chemistry, University of Ioannina, Ioannina, Greece.
J Cardiovasc Pharmacol Ther. 2015 May;20(3):276-83. doi: 10.1177/1074248414549419. Epub 2014 Sep 18.
Prediabetes substantially increases cardiovascular risk. We examined the effect of rosuvastatin on the quantity and quality of low-density lipoprotein cholesterol (LDL-C) in patients with dyslipidemia having impaired fasting glucose (IFG) compared to normoglycemic patients with dyslipidemia.
This was a prospective observational study including patients with dyslipidemia and IFG (IFG group, n = 49) matched with normoglycemic patients with dyslipidemia (control group, n = 64). Study participants, following dietary intervention, were prescribed rosuvastatin 10 or 20 mg/d to achieve LDL-C goals. Baseline as well as 24 weeks posttreatment changes in the serum lipid profile were evaluated. Moreover, analysis of the LDL subfraction profile was conducted using a polyacrylamide tube gel electrophoresis method.
Similar effects were observed in lipid profile in both treatment groups. Patients with IFG experienced a greater decrease in the cholesterol concentration of small dense LDL particles (-65.7%, P < .001 vs baseline) compared to controls (-38.5%, P < .001 vs baseline; P = .018 vs patients with IFG). There was no significant difference in the changes of cholesterol concentration of large and buoyant LDL particles in the IFG group when compared to the control group. A greater increase in the mean LDL particle size (+1.5%, P < .001 vs baseline) was noted in the IFG group compared to the control group at 24 weeks (+0.4%, P = .028 vs baseline; P = .008 vs IFG group).
Targeting dyslipidemia with rosuvastatin was associated with more favorable changes in the LDL subfraction profile in patients with IFG compared to normoglycemic ones.
糖尿病前期会显著增加心血管疾病风险。我们比较了瑞舒伐他汀对空腹血糖受损(IFG)的血脂异常患者与血糖正常的血脂异常患者低密度脂蛋白胆固醇(LDL-C)的数量和质量的影响。
这是一项前瞻性观察性研究,纳入了血脂异常合并IFG的患者(IFG组,n = 49),并与血糖正常的血脂异常患者(对照组,n = 64)进行匹配。研究参与者在饮食干预后,服用10或20 mg/d的瑞舒伐他汀以实现LDL-C目标。评估了基线以及治疗24周后血清脂质谱的变化。此外,使用聚丙烯酰胺管凝胶电泳法对LDL亚组分谱进行分析。
两个治疗组在脂质谱方面观察到相似的效果。与对照组相比,IFG患者小而密LDL颗粒的胆固醇浓度下降幅度更大(-65.7%,与基线相比P <.001;对照组为-38.5%,与基线相比P <.001;与IFG患者相比P = 0.018)。与对照组相比,IFG组大而轻LDL颗粒的胆固醇浓度变化无显著差异。与对照组相比,IFG组在24周时平均LDL颗粒大小增加幅度更大(+1.5%,与基线相比P <.001;对照组为+0.4%,与基线相比P = 0.028;与IFG组相比P = 0.008)。
与血糖正常的患者相比,使用瑞舒伐他汀治疗血脂异常在IFG患者中与LDL亚组分谱更有利的变化相关。