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The efficacy and safety of ezetimibe/simvastatin combination compared with intensified lipid‐lowering treatment strategies in diabetic subjects with and without metabolic syndrome
Author(s) -
Jimenez J. G.,
Rosen J. B.,
Pirags V.,
Massaad R.,
Hanson M. E.,
Brudi P.,
Triscari J.
Publication year - 2013
Publication title -
diabetes, obesity and metabolism
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.445
H-Index - 128
eISSN - 1463-1326
pISSN - 1462-8902
DOI - 10.1111/dom.12059
Subject(s) - ezetimibe , simvastatin , rosuvastatin , medicine , statin , tolerability , atorvastatin , metabolic syndrome , apolipoprotein b , cholesterol , endocrinology , diabetes mellitus , pharmacology , adverse effect
Aims The objective was to assess the consistency of effect of switching to ezetimibe/simvastatin 10/20 mg versus doubling the baseline statin dose (to simvastatin 40 mg or atorvastatin 20 mg) or switching to rosuvastatin 10 mg across subgroups of subjects with (n = 617) and without (n = 191) metabolic syndrome ( MetS ). Methods This was a post hoc analysis of a randomized, double‐blind, 6‐week study of adults 18–79 years with cardiovascular disease and diabetes mellitus with low‐density lipoprotein cholesterol ( LDL ‐C) ≥70 and ≤160 mg/dl. The percent change in LDL ‐C and other lipids was estimated within each subgroup separately. Safety and tolerability were assessed. Results In subjects with MetS , percent changes in LDL ‐C and other lipids were greater with ezetimibe/simvastatin versus doubling baseline statin or numerically greater versus switching to rosuvastatin, except high‐density lipoprotein cholesterol and apolipoprotein (Apo) AI (mean percent changes in LDL ‐C were: −22.49% ezetimibe/simvastatin, −9.64% doubled baseline statin and −19.20% rosuvastatin). In subjects without MetS , percent changes in LDL ‐C, total cholesterol and Apo B were greater with ezetimibe/simvastatin versus doubling baseline statin or numerically greater versus switching to rosuvastatin (mean percent changes in LDL ‐C were: −25.14% ezetimibe/simvastatin, −4.75% doubled baseline statin and −19.75% rosuvastatin). Safety profiles were generally similar. Conclusion These results showed that switching to ezetimibe/simvastatin 10/20 mg was more effective at reducing LDL ‐C, total cholesterol and Apo B versus doubling the baseline statin dose to simvastatin 40 mg or atorvastatin 20 mg or switching to rosuvastatin 10 mg regardless of MetS status. These results were generally similar to those of the full cohort.