Relationships Between Metabolic Syndrome and Other Baseline Factors and the Efficacy of Ezetimibe/simvastatin and Atorvastatin in Patients with Type 2 Diabetes and Hypercholesterolemia
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Objective: To investigate relationships between baseline factors and treatment-associated efficacy changes in type 2 diabetes.
Research Design: AND METHODS Multivariable analyses of treatment response in 1,229 type 2 diabetic patients with hypercholesterolemia who received ezetimibe/simvastatin or atorvastatin in a randomized double-blind 6-week study.
Results: Increasing age was related to improvements in all lipid assessments. Men had greater triglyceride and non-HDL cholesterol reductions than women, and black/Hispanic patients had less favorable lipid effects than other races/ethnicities. Increasing baseline LDL cholesterol was associated with improvements in most lipids; higher baseline non-HDL cholesterol with improved HDL cholesterol and triglycerides; higher baseline HDL cholesterol with greater non-HDL cholesterol and high-sensitivity C-reactive protein (hs-CRP) reductions; and higher baseline hs-CRP with smaller LDL cholesterol, non-HDL cholesterol, and apolipoprotein B reductions. Patients with high baseline non-HDL cholesterol or triglycerides less frequently attained LDL cholesterol targets. Obesity was inversely related to HDL cholesterol and hs-CRP changes, and higher baseline A1C to smaller apolipoprotein B reductions. Metabolic syndrome was not a significant predictor.
Conclusions: Treatment responses in type 2 diabetic patients were related to baseline factors, although treatment effects (ezetimibe/simvastatin being more effective than atorvastatin) remained consistent. The presence of predictive factors should be considered in planning lipid-altering therapy.
Yamaguchi S, Oba K, Higa M, Arasaki O, Shimabukuro M J Clin Med. 2020; 9(6).
PMID: 32492927 PMC: 7356893. DOI: 10.3390/jcm9061675.
Sergeev I, Keren N, Naftali T, Konikoff F Dig Dis Sci. 2019; 65(4):1223-1230.
PMID: 31522322 DOI: 10.1007/s10620-019-05823-z.
Spinedi E, Cardinali D Int J Endocrinol. 2018; 2018:1349868.
PMID: 30147722 PMC: 6083563. DOI: 10.1155/2018/1349868.
Bentley A, Rotimi C Expert Rev Endocrinol Metab. 2017; 7(6):659-667.
PMID: 28191028 PMC: 5298839. DOI: 10.1586/eem.12.55.
Ohbu-Murayama K, Adachi H, Hirai Y, Enomoto M, Fukami A, Obuchi A J Diabetes Investig. 2015; 6(3):325-33.
PMID: 25969718 PMC: 4420565. DOI: 10.1111/jdi.12298.