Kumar Manoj, Rehan Harmeet Singh, Puri Raman, Yadav Madhur, Gupta Lalit Kumar
Department of Pharmacology, Lady Hardinge Medical College and associated Hospitals, New Delhi, India.
Department of Pharmacology, Lady Hardinge Medical College and associated Hospitals, New Delhi, India.
Indian Heart J. 2018 Dec;70 Suppl 3(Suppl 3):S64-S67. doi: 10.1016/j.ihj.2018.05.010. Epub 2018 May 26.
Data regarding efficacy comparison of daily regimen (DR) versus every other day regimen (EODR) atorvastatin therapy is not validated by estimation of serum hydroxymethylglutaryl-CoA reductase (HMGCR) levels and HMGCR correlation with lipid indices.
In this randomized controlled trial, we compared the efficacy of DR versus EODR by measuring lipid indices and serum HMGCR levels at baseline and after 12 weeks of 10 mg atorvastatin therapy. Primary endpoint was comparison of mean change in serum HMGCR levels and lipid indices of both groups and their correlation with each other. Secondary endpoints were assessed by estimating serum aspartate aminotransferase (AST), alanine aminotransferase (ALT) and creatine kinase MM (CK-MM) levels and adverse drug reactions (ADRs).
A total of 61 patients were enrolled of which 46 completed the study (24 in DR vs 22 in EODR group). The mean reduction in total cholesterol (TC), low density lipoprotein-cholesterol (LDL-C) and non-high density lipoprotein-cholesterol (HDL-C) was significantly higher in DR group, whereas mean reduction in triglycerides (TG) and increase in HDL-C was similar in both the groups. Reduction in serum HMGCR levels was comparable in both the groups (31.17% vs 28.19%). Change in serum HMGCR levels correlated more with change in lipid indices of DR group. Also, safety parameters were similar between the two groups.
Both the regimens achieved therapeutic goals, however DR was found to be superior as it achieved greater reduction in TC and LDL-C. Further, these findings are substantiated by correlation of lipid indices with serum HMGCR levels.
通过估计血清羟甲基戊二酰辅酶A还原酶(HMGCR)水平以及HMGCR与血脂指标的相关性,验证每日给药方案(DR)与隔日给药方案(EODR)阿托伐他汀治疗效果比较的数据。
在这项随机对照试验中,我们通过在基线以及10mg阿托伐他汀治疗12周后测量血脂指标和血清HMGCR水平,比较了DR与EODR的疗效。主要终点是比较两组血清HMGCR水平和血脂指标的平均变化及其相互关系。次要终点通过估计血清天冬氨酸氨基转移酶(AST)、丙氨酸氨基转移酶(ALT)和肌酸激酶MM(CK-MM)水平以及药物不良反应(ADR)来评估。
共纳入61例患者,其中46例完成研究(DR组24例,EODR组22例)。DR组总胆固醇(TC)、低密度脂蛋白胆固醇(LDL-C)和非高密度脂蛋白胆固醇(non-HDL-C)的平均降低幅度显著更高,而两组甘油三酯(TG)的平均降低幅度和高密度脂蛋白胆固醇(HDL-C)的升高幅度相似。两组血清HMGCR水平的降低幅度相当(31.17%对28.19%)。血清HMGCR水平的变化与DR组血脂指标的变化相关性更强。此外,两组的安全性参数相似。
两种给药方案均达到了治疗目标,但发现DR方案更优,因为它在降低TC和LDL-C方面效果更显著。此外,血脂指标与血清HMGCR水平的相关性证实了这些发现。