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The effects of simvastatin treatment on plasma lipid-related biomarkers in men with dyslipidaemia

机译:辛伐他汀治疗对血脂异常男性血浆脂质相关生物标志物的影响

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Background: Lipidomic biomarkers will facilitate the development of novel anti-atherosclerotic therapies. Objective:To evaluate the responses of circulating biomarkers to simvastatin treatment. Methods: A randomized, cross-over study in men with mixed dyslipidaemia was used to compare effects of simvastatin 40 mg/day with placebo. Results: Plasma concentrations of nine fatty acids (FA; of 33 evaluated) were reduced significantly by simvastatin. No changes in the rates of FA synthesis or in hepatic lipase or lipoprotein lipase activities were apparent. Circulating proprotein convertase subtilisin/kexin type 9 (PCSK9) levels increased. Conclusion: We identified lipidomic biomarkers of simvastatin treatment effect that are consistent with statin inhibition of 3-hydroxy-3-methyl-glutaryl coenzyme A (HMG-CoA) reductase (ClinicalTrials.gov: NCT00935259).
机译:背景:脂质生物标志物将促进新型抗动脉粥样硬化疗法的发展。目的:评估循环生物标志物对辛伐他汀治疗的反应。方法:一项针对混合型血脂异常男性患者的随机,交叉研究用于比较辛伐他汀40 mg /天与安慰剂的疗效。结果:辛伐他汀可显着降低9种脂肪酸(FA; 33种评估血浆)的血浆浓度。 FA合成速率或肝脂肪酶或脂蛋白脂肪酶活性没有明显变化。循环前蛋白转化酶枯草杆菌蛋白酶/ kexin 9型(PCSK9)水平升高。结论:我们确定了辛伐他汀治疗效果的脂质组学生物标志物,与他汀类药物抑制3-羟基-3-甲基-谷氨酰辅酶A(HMG-CoA)还原酶一致(ClinicalTrials.gov:NCT00935259)。

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