Lipid-altering efficacy of ezetimibe/simvastatin 10/20 mg compared to rosuvastatin 10 mg in high-risk patients with and without type 2 diabetes mellitus inadequately controlled despite prior statin monotherapy
Language English Country Great Britain, England Media print-electronic
Document type Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial, Research Support, Non-U.S. Gov't
PubMed
20626402
DOI
10.1111/j.1755-5922.2010.00181.x
PII: CDR181
Knihovny.cz E-resources
- MeSH
- Anticholesteremic Agents adverse effects therapeutic use MeSH
- Apolipoproteins B metabolism MeSH
- Azetidines adverse effects therapeutic use MeSH
- C-Reactive Protein metabolism MeSH
- Cholesterol blood MeSH
- Diabetes Mellitus, Type 2 blood MeSH
- Double-Blind Method MeSH
- Ezetimibe MeSH
- Fluorobenzenes adverse effects therapeutic use MeSH
- Hypercholesterolemia blood drug therapy MeSH
- Drug Therapy, Combination MeSH
- Cholesterol, LDL blood MeSH
- Drug Resistance MeSH
- Humans MeSH
- Lipids blood MeSH
- Odds Ratio MeSH
- Pyrimidines adverse effects therapeutic use MeSH
- Rosuvastatin Calcium MeSH
- Simvastatin adverse effects therapeutic use MeSH
- Hydroxymethylglutaryl-CoA Reductase Inhibitors adverse effects therapeutic use MeSH
- Sulfonamides adverse effects therapeutic use MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Multicenter Study MeSH
- Research Support, Non-U.S. Gov't MeSH
- Randomized Controlled Trial MeSH
- Comparative Study MeSH
- Names of Substances
- Anticholesteremic Agents MeSH
- Apolipoproteins B MeSH
- Azetidines MeSH
- C-Reactive Protein MeSH
- Cholesterol MeSH
- Ezetimibe MeSH
- Fluorobenzenes MeSH
- Cholesterol, LDL MeSH
- Lipids MeSH
- Pyrimidines MeSH
- Rosuvastatin Calcium MeSH
- Simvastatin MeSH
- Hydroxymethylglutaryl-CoA Reductase Inhibitors MeSH
- Sulfonamides MeSH
AIMS: This post hoc analysis compared the effects of switching to ezetimibe/simvastatin 10/20 mg (EZE/SIMVA) or rosuvastatin 10 mg (ROSUVA) in uncontrolled high-risk hypercholesterolemic patients with/without type 2 diabetes mellitus (T2DM) despite statin monotherapy. METHODS: Patients (n = 618) at high risk for coronary vascular disease with elevated LDL-C ≥100 and ≤190 mg/dL despite use of statins were randomized 1:1 to double-blind EZE/SIMVA 10/20 mg or ROSUVA 10 mg for 6 weeks. Patients were classified as having T2DM based on ≥1 of the following: diagnosis of T2DM, antidiabetic medication, or FPG ≥126 mg/dL. This analysis evaluated percent changes from baseline in lipids among patients with (n = 182) and without T2DM (n = 434). RESULTS: EZE/SIMVA was more effective than ROSUVA at lowering LDL-C, TC, non-HDL-C, and apo B in the overall study population and within both subgroups. Numerically, greater between-treatment reductions in LDL-C, TC, non-HDL-C, and apo B were seen in patients with T2DM versus those without T2DM. A significant interaction (P= 0.015) was seen for LDL-C indicating that patients with T2DM achieved larger between-group reductions versus those without T2DM. CONCLUSIONS: Switching to EZE/SIMVA 10/20 mg versus ROSUVA 10 mg provided superior lipid reductions in patients with/without T2DM.
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