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Efficacy of Atorvastatin for Achieving Cholesterol Targets After LDL-Cholesterol Based Dose Selection in Patients With Type 2 Diabetes

Division of Diabetes, Consortium University General Hospital of Valencia, ferrer_juagar{at}gva.es

Eva Sanchez-Ballester, MD

Department of Internal Medicine, Consortium University General Hospital of Valencia, Valencia, Spain

Raquel Albalat-Galera

Division of Diabetes, Consortium University General Hospital of Valencia

Miguel Berzosa-Sanchez, MD

Department of Internal Medicine, Consortium University General Hospital of Valencia, Valencia, Spain

Agustín Herrera-Ballester, MD, PhD

Department of Internal Medicine, Consortium University General Hospital of Valencia, Valencia, Spain

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 tryglicerides 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.

Key Words: atorvastatin • type 2 diabetes • dyslipidemia • low-density lipoprotein cholesterol

This version was published on September 1, 2008

Journal of Cardiovascular Pharmacology and Therapeutics, Vol. 13, No. 3, 183-188 (2008)
DOI: 10.1177/1074248408321461


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