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阿托伐他汀在2型糖尿病患者基于低密度脂蛋白胆固醇的剂量选择后实现胆固醇目标的疗效。

Efficacy of atorvastatin for achieving cholesterol targets after LDL-cholesterol based dose selection in patients with type 2 diabetes.

作者信息

Ferrer-García Juan Carlos, Sanchez-Ballester Eva, Albalat-Galera Raquel, Berzosa-Sanchez Miguel, Herrera-Ballester Agustín

机构信息

Division of Diabetes, Consortium University General Hospital of Valencia, Spain.

出版信息

J Cardiovasc Pharmacol Ther. 2008 Sep;13(3):183-8. doi: 10.1177/1074248408321461. Epub 2008 Jul 17.

Abstract

We analyzed the feasibility of an intensive lipid-lowering strategy based on a starting dose of atorvastatin according to baseline and target low-density lipoprotein cholesterol (LDL-C) level (<2.6 mmol/L) in 202 statin-naïve patients with type 2 diabetes within 24 weeks. They were assigned to receive a daily dosage of atorvastatin based on their initial LDL-C levels. The primary endpoint was the proportion of patients achieving the LDL-C goal after 24 weeks of treatment. No changes were made in prescribed atorvastatin dosage. At the study end, 66.5% of the 188 patients completing the trial reached the LDL-C target (75%, 67%, 58% and 59% with 10, 20, 40 and 80 mg per day of atorvastatin, respectively) reached LDL-C target. Atorvastatin reduced the levels of total cholesterol, LDL-C, high density lipoprotein cholesterol (HDL-C) and triglycerides by 29%, 35%, 3% and 22%, respectively, and all statin doses were well tolerated. Thus, individualizing the starting dose of atorvastatin according to baseline and target LDL-C levels, allowed a high proportion of type 2 diabetic patients to achieve the target within 24 weeks.

摘要

我们分析了在24周内,根据202例初治2型糖尿病患者的基线和目标低密度脂蛋白胆固醇(LDL-C)水平(<2.6 mmol/L),采用阿托伐他汀起始剂量的强化降脂策略的可行性。根据他们最初的LDL-C水平,将他们分配接受每日剂量的阿托伐他汀。主要终点是治疗24周后达到LDL-C目标的患者比例。阿托伐他汀的处方剂量未作改变。在研究结束时,完成试验的188例患者中有66.5%达到了LDL-C目标(每天服用10、20、40和80毫克阿托伐他汀的患者分别为75%、67%、58%和59%)。阿托伐他汀使总胆固醇、LDL-C、高密度脂蛋白胆固醇(HDL-C)和甘油三酯水平分别降低了29%、35%、3%和22%,所有他汀类药物剂量耐受性良好。因此,根据基线和目标LDL-C水平个体化阿托伐他汀的起始剂量,可使高比例的2型糖尿病患者在24周内达到目标。

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