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Metabolic Alterations Associated with Atorvastatin/Fenofibric Acid Combination in Patients with Atherogenic Dyslipidaemia: A Randomized Trial for Comparison with Escalated-Dose Atorvastatin

机译:代谢改变与阿托伐他汀/非诺贝特酸联合在无源性血脂异常患者中的应用:阿托伐他汀与递增剂量阿托伐他汀比较的随机试验

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摘要

In the current study, the metabolic effects of atorvastatin dose escalation versus atorvastatin/fenofibric acid combination were compared using metabolomics analyses. Men and women with combined hyperlipidaemia were initially prescribed atorvastatin (10 mg, ≥4 weeks). Patients who reached low-density lipoprotein-cholesterol targets, but had triglyceride and high-density lipoprotein-cholesterol levels ≥150 mg/dL and <50 mg/dL, respectively, were randomized to receive atorvastatin 20 mg or atorvastatin 10 mg/fenofibric acid 135 mg for 12 weeks. Metabolite profiling of serum was performed and changes in metabolites after drug treatment in the two groups were compared. Analysis was performed using patients’ samples obtained before and after treatment. Of 89 screened patients, 37 who met the inclusion criteria were randomized, and 34 completed the study. Unlike that in the dose-escalation group, distinct clustering of both lipid and aqueous metabolites was observed in the combination group after treatment. Most lipid metabolites of acylglycerols and many of ceramides decreased, while many of sphingomyelins increased in the combination group. Atorvastatin dose escalation modestly decreased lysophosphatidylcholines; however, the effect of combination therapy was variable. Most aqueous metabolites decreased, while l-carnitine remarkably increased in the combination group. In conclusion, the atorvastatin/fenofibric acid combination induced distinct metabolite clustering. Our results provide comprehensive information regarding metabolic changes beyond conventional lipid profiles for this combination therapy.
机译:在当前的研究中,使用代谢组学分析比较了阿托伐他汀剂量增加与阿托伐他汀/非诺贝酸联合的代谢作用。合并高脂血症的男性和女性最初应服用阿托伐他汀(10毫克,≥4周)。达到低密度脂蛋白胆固醇目标但甘油三酸酯和高密度脂蛋白胆固醇水平分别≥150mg / dL和<50 mg / dL的患者被随机分配接受阿托伐他汀20 mg或阿托伐他汀10 mg /非诺贝酸135mg,持续12周。进行血清代谢物谱分析,比较两组药物治疗后代谢物的变化。使用治疗前后获得的患者样本进行分析。在89例筛查患者中,将37例符合纳入标准的患者随机分组,其中34例完成了研究。与剂量递增组不同,治疗后在联合组中观察到脂质和水代谢产物的明显聚集。在联合治疗组中,大多数酰基甘油的脂质代谢产物和许多神经酰胺减少,而许多鞘磷脂则增加。阿托伐他汀剂量增加适度地降低了溶血磷脂酰胆碱。然而,联合治疗的效果是可变的。在组合组中,大多数水性代谢物减少,而左旋肉碱显着增加。总之,阿托伐他汀/非诺贝特酸联合诱导明显的代谢物聚集。我们的结果提供了有关该联合疗法超出常规脂质谱的代谢变化的综合信息。

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