Effect of fixed-dose combinations of ezetimibe plus rosuvastatin in patients with primary hypercholesterolemia: MRS-ROZE (Multicenter Randomized Study of ROsuvastatin and eZEtimibe).

Published

Journal Article

We aimed to compare the effects of fixed-dose combinations of ezetimibe plus rosuvastatin to rosuvastatin alone in patients with primary hypercholesterolemia, including a subgroup analysis of patients with diabetes mellitus (DM) or metabolic syndrome (MetS).This multicenter eight-week randomized double-blind phase III study evaluated the safety and efficacy of fixed-dose combinations of ezetimibe 10 mg plus rosuvastatin, compared with rosuvastatin alone in patients with primary hypercholesterolemia. Four hundred and seven patients with primary hypercholesterolemia who required lipid-lowering treatment according to the ATP III guideline were randomized to one of the following six treatments for 8 weeks: fixed-dose combinations with ezetimibe 10 mg daily plus rosuvastatin (5, 10, or 20 mg daily) or rosuvastatin alone (5, 10, or 20 mg daily).Fixed-dose combination of ezetimibe plus rosuvastatin significantly reduced LDL cholesterol, total cholesterol, and triglyceride levels compared with rosuvastatin alone. Depending on the rosuvastatin dose, these fixed-dose combinations of ezetimibe plus rosuvastatin provided LDL cholesterol, total cholesterol, and triglyceride reductions of 56%-63%, 37%-43%, and 19%-24%, respectively. Moreover, the effect of combination treatment on cholesterol levels was more pronounced in patients with DM or MetS than in non-DM or non-MetS patients, respectively, whereas the effect of rosuvastatin alone did not differ between DM vs non-DM or MetS vs non-MetS patients.Fixed-dose combinations of ezetimibe and rosuvastatin provided significantly superior efficacy to rosuvastatin alone in lowering LDL cholesterol, total cholesterol, and triglyceride levels. Moreover, the reduction rate was greater in patients with DM or MetS.

Full Text

Cited Authors

  • Kim, K-J; Kim, S-H; Yoon, YW; Rha, S-W; Hong, S-J; Kwak, C-H; Kim, W; Nam, C-W; Rhee, M-Y; Park, T-H; Hong, T-J; Park, S; Ahn, Y; Lee, N; Jeon, H-K; Jeon, D-W; Han, K-R; Moon, K-W; Chae, I-H; Kim, H-S

Published Date

  • October 2016

Published In

Volume / Issue

  • 34 / 5

Start / End Page

  • 371 - 382

PubMed ID

  • 27506635

Pubmed Central ID

  • 27506635

Electronic International Standard Serial Number (EISSN)

  • 1755-5922

International Standard Serial Number (ISSN)

  • 1755-5914

Digital Object Identifier (DOI)

  • 10.1111/1755-5922.12213

Language

  • eng