Achievement of Specified Low-density Lipoprotein Cholesterol, Non-high-density Lipoprotein Cholesterol Apolipoprotein B, and High-sensitivity C-reactive Protein Levels with Ezetimibe/simvastatin or Atorvastatin in Metabolic Syndrome Patients With...
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Endocrinology
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Background: Metabolic syndrome (MetS) and atherosclerotic vascular disease (AVD) are associated with increased coronary heart disease risk.
Objective: To assess percent change from baseline in lipids and high-sensitivity C-reactive protein (hs-CRP) levels and the proportion of subjects reaching specified low-density lipoprotein cholesterol (LDL-C), non-high-density lipoprotein cholesterol (HDL-C) and apolipoprotein B (Apo B) single, dual, and triple targets and hs-CRP <2 mg/L among subjects with and without AVD treated with ezetimibe/simvastatin or atorvastatin for 6 weeks.
Methods: Adults (N = 1143) with MetS and hypercholesterolemia were randomized to starting and next higher doses of ezetimibe/simvastatin (10/20 or 10/40 mg) or atorvastatin (10, 20, or 40 mg).
Results: Ezetimibe/simvastatin produced significantly greater reductions in evaluated lipids than atorvastatin for most prespecified dose comparisons. More subjects without AVD achieved LDL-C levels <100 mg/dL, non-HDL-C levels <130 mg/dL, and dual LDL-C/non-HDL targets (83%-92% vs 62%-76%) and Apo B <90 mg/dL or triple targets (65%-75% vs 41%-49%) with 40 mg of atorvastatin or 10/20-40 mg of ezetimibe/simvastatin compared with 10 or 20 mg of atorvastatin, respectively. More subjects with AVD achieved LDL-C<70 mg/dL and non-HDL-C<100 mg/dL single and dual targets (65%-80%) and Apo B <80 mg/dL (53%-63%) with 10/20-40 mg of ezetimibe/simvastatin than with 40 mg of atorvastatin (40%-49%). More subjects achieved triple lipid targets with 10/20-40 mg of ezetimibe/simvastatin versus 10-40 mg of atorvastatin (50%-63% vs 24%-40%). Achievement of hs-CRP <2 mg/L was similar across all doses regardless of AVD status.
Conclusions: More intensive therapy was required for >80% of subjects to achieve LDL-C <100 mg/dL and non-HDL-C <130 mg/dL and for the majority of subjects to achieve lower levels of LDL-C <70 mg/dL, non-HDL-C <100 mg/dL, and/or Apo B <90 mg/dL. The effect of ezetimibe on cardiovascular risk reduction has yet to be established. (Clintrials.gov no: NCT00409773).
Yang J, Zhang R, Han B, Li H, Wang J, Xiao Y Lipids Health Dis. 2024; 23(1):271.
PMID: 39198852 PMC: 11351259. DOI: 10.1186/s12944-024-02244-4.
Arabi S, Chambari M, Malek-Ahmadi M, Bahrami L, Hadi V, Rizzo M Inflammopharmacology. 2022; 30(5):1597-1615.
PMID: 35988111 DOI: 10.1007/s10787-022-01053-4.
Reduction of Vascular Inflammation, LDL-C, or Both for the Protection from Cardiovascular Events?.
Reklou A, Doumas M, Imprialos K, Stavropoulos K, Patoulias D, Athyros V Open Cardiovasc Med J. 2018; 12:29-40.
PMID: 29785212 PMC: 5897979. DOI: 10.2174/1874192401812010029.
Lai J, Wu B, Xuan T, Xia S, Liu Z, Chen J J Clin Med Res. 2015; 7(6):446-52.
PMID: 25883708 PMC: 4394918. DOI: 10.14740/jocmr2124w.
Lipid-lowering efficacy of atorvastatin.
Adams S, Tsang M, Wright J Cochrane Database Syst Rev. 2015; (3):CD008226.
PMID: 25760954 PMC: 6464917. DOI: 10.1002/14651858.CD008226.pub3.