Title of article
Lipid-Altering Efficacy and Safety of Ezetimibe/Simvastatin Coadministered With Extended-Release Niacin in Patients With Type IIa or Type IIb Hyperlipidemia Original Research Article
Author/Authors
John R. Guyton، نويسنده , , B. Greg Brown، نويسنده , , Sergio Fazio، نويسنده , , Adam Polis، نويسنده , , Joanne E. Tomassini، نويسنده , , Andrew M. Tershakovec، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
9
From page
1564
To page
1572
Abstract
Objectives
This study evaluated the safety and lipid-altering efficacy of ezetimibe/simvastatin (E/S) coadministered with extended-release niacin (N) in patients with type IIa or IIb hyperlipidemia.
Background
Current guidelines recommend consideration of combination drug therapy to achieve optimal low-density lipoprotein cholesterol (LDL-C) lowering and broader lipid-altering effects when treating hypercholesterolemic patients at high risk for atherosclerotic cardiovascular events.
Methods
In this 24-week multicenter, randomized, double-blind study, 1,220 type IIa or IIb hyperlipidemic patients were randomized to treatment with E/S (10/20 mg/day) + N (titrated to 2 g/day), or N (titrated to 2 g/day), or E/S (10/20 mg/day). Changes from baseline in LDL-C (primary) and other secondary variables were assessed in the completers and modified intent-to-treat populations.
Results
Coadministered E/S with N resulted in significantly greater reductions in LDL-C, non–high-density lipoprotein cholesterol, triglycerides, apolipoprotein B, and lipid/lipoprotein ratios, compared with either agent alone (p < 0.001). The combination increased levels of apolipoprotein A-I and high-density lipoprotein cholesterol significantly more than E/S (p < 0.001), and reduced high-sensitivity C-reactive protein levels significantly more than N (p = 0.005). A significantly greater percentage of patients discontinued the study in the N (25.0%) and E/S + N (23.3%) groups, compared with E/S (9.6%, p < 0.001) because of clinical adverse experiences (primarily flushing). Incidences of other clinical and laboratory adverse experiences (liver-, muscle-, and gastrointestinal-related) were similar for all groups.
Conclusions
Combination treatment with E/S plus N showed superior lipid-altering efficacy compared with N or E/S in type IIa or IIb hyperlipidemia patients and was generally well tolerated aside from N-associated flushing. This combination offers an effective, broad, lipid-altering therapy with improvements in lipid effects beyond LDL-C in these patients. (To Evaluate Ezetimibe/Simvastatin and Niacin [Extended Release Tablet] in Patients With High Cholesterol; NCT00271817)
Keywords
coronary heart disease , Creatine kinase , HDL-C , apolipoprotein , TC , total cholesterol , N , LDL-C , CK , AE , apo , CHD , high-density lipoprotein cholesterol , low-density lipoprotein cholesterol , HSCRP , high-sensitivity C-reactive protein , ULN , upper limit of normal , adverse experience , E/S , ezetimibe/simvastatin , LOCF , last observation carried forward , mITT , modified intent-to-treat , extended-release niacin
Journal title
JACC (Journal of the American College of Cardiology)
Serial Year
2008
Journal title
JACC (Journal of the American College of Cardiology)
Record number
473261
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