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依折麦布/辛伐他汀与辛伐他汀在伴有或不伴有糖尿病的冠心病患者中的应用比较。

Ezetimibe/simvastatin vs simvastatin in coronary heart disease patients with or without diabetes.

机构信息

Dipartimenti Fisiopatologia Clinica, Universitàd i Firenze, Viale Pieraccini 6, 50139, Florence, Italy.

出版信息

Lipids Health Dis. 2010 Jul 27;9:80. doi: 10.1186/1476-511X-9-80.

Abstract

BACKGROUND

Treatment guidelines recommend LDL-C as the primary target of therapy in patients with hypercholesterolemia. Moreover, combination therapies with lipid-lowering drugs that have different mechanisms of action are recommended when it is not possible to attain LDL-C targets with statin monotherapy. Understanding which treatment or patient-related factors are associated with attaining a target may be clinically relevant.

METHODS

Data were pooled from two multicenter, randomized, double-blind studies. After stabilization on simvastatin 20 mg, patients with coronary heart disease (CHD) alone and/or type 2 diabetes mellitus (T2DM) were randomized to ezetimibe 10 mg/simvastatin 20 mg (EZ/Simva) or simvastatin 40 mg. The change from baseline in low-density lipoprotein cholesterol (LDL-C), total cholesterol (TC), high-density lipoprotein cholesterol (HDL-C), TC/HDL-C ratio, triglycerides, and the proportion of patients achieving LDL-C < 2.6 mmol/L (100 mg/dL) after 6 weeks of treatment were assessed, and factors significantly correlated with the probability of achieving LDL-C < 2.6 mmol/L in a population of high cardiovascular risk Italian patients were identified. A stepwise logistic regression model was conducted with LDL-C < 2.6 mmol/L at endpoint as the dependent variable and study, treatment, gender, age (> or = 65 years or < 65 years), as independent variables and baseline LDL-C (both as continuous and discrete variable).

RESULTS

EZ/Simva treatment (N = 93) resulted in significantly greater reductions in LDL-C, TC, and TC/HDL-C ratio and higher attainment of LDL-C < 2.6 mmol/L vs doubling the simvastatin dose to 40 mg (N = 106). Study [including diabetic patients (OR = 2.9, p = 0.003)], EZ/Simva treatment (OR = 6.1, p < 0.001), and lower baseline LDL-C (OR = 0.9, p = 0.001) were significant positive predictors of LDL-C target achievement. When baseline LDL-C was expressed as a discrete variable, the odds of achieving LDL-C < 2.6 mmol/L was 4.8 in favor of EZ/Simva compared with Simva 40 mg (p < 0.001), regardless of baseline LDL-C level.

CONCLUSION

EZ/Simva is an effective therapeutic option for patients who have not achieved recommended LDL-C treatment targets with simvastatin 20 mg monotherapy.

TRIAL REGISTRATION

Clinical trial registration numbers: NCT00423488 and NCT00423579.

摘要

背景

治疗指南建议将 LDL-C 作为高胆固醇血症患者治疗的主要目标。此外,当单独使用他汀类药物无法达到 LDL-C 目标时,建议使用具有不同作用机制的降脂药物联合治疗。了解哪些治疗或患者相关因素与达到目标相关可能具有临床意义。

方法

数据来自两项多中心、随机、双盲研究。在稳定使用辛伐他汀 20mg 后,单独患有冠心病 (CHD) 和/或 2 型糖尿病 (T2DM) 的患者被随机分配至依折麦布 10mg/辛伐他汀 20mg (EZ/Simva) 或辛伐他汀 40mg。评估治疗 6 周后 LDL-C、总胆固醇 (TC)、高密度脂蛋白胆固醇 (HDL-C)、TC/HDL-C 比值、甘油三酯的基线变化,以及达到 LDL-C<2.6mmol/L(100mg/dL)的患者比例,并确定意大利高心血管风险患者人群中与 LDL-C<2.6mmol/L 达标概率显著相关的因素。采用逐步逻辑回归模型,以 LDL-C<2.6mmol/L 作为因变量,研究、治疗、性别、年龄(≥65 岁或<65 岁)作为自变量,基线 LDL-C(连续和离散变量)作为因变量。

结果

与双倍剂量辛伐他汀 40mg 相比,依折麦布联合辛伐他汀治疗 (N=93) 可显著降低 LDL-C、TC 和 TC/HDL-C 比值,并且 LDL-C<2.6mmol/L 的达标率更高。研究[包括糖尿病患者(OR=2.9,p=0.003)]、依折麦布联合辛伐他汀治疗 (OR=6.1,p<0.001) 和较低的基线 LDL-C(OR=0.9,p=0.001)是 LDL-C 目标达标显著的正预测因子。当以离散变量表示基线 LDL-C 时,与辛伐他汀 40mg 相比,依折麦布联合辛伐他汀治疗 LDL-C<2.6mmol/L 的优势比为 4.8(p<0.001),而与基线 LDL-C 水平无关。

结论

对于辛伐他汀 20mg 单药治疗未达到 LDL-C 治疗目标的患者,依折麦布联合辛伐他汀治疗是一种有效的治疗选择。

试验注册

临床试验注册号:NCT00423488 和 NCT00423579。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd57/2918617/8ee06630b024/1476-511X-9-80-1.jpg

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