A single center, open label, randomized, clinical trial comparing ApoB/ApoA ratio of Vytorin 10/20mg vs atorvastatin 20mg treatment. DM2 patients will be screened for inclusion criteria. Patients (n=66 in each arm) will be randomized to either Ezetimibe/simvastatin 10/20mg or atorvastatin 20mg after 4 week washout or TLC period. Primary and secondary endpoints will be assessed at week 12. Primary endpoint: 1\) change of ApoB/ApoA ratio at week 12. Secondary endpoint: 1. Change of lipid parameters (TC, LDL-C, HDL-C, TG, apoB 48) at week 12. 2. Change of HbA1C at week 12. 3. Change of HOMA index at week 12 \- HOMA =\[Fasting insulin (mIU/L) × Fasting glucose (mmol/L)\] / 22.5 4. Change of hsCRP at week 12 5. Safety assessment Hypotheses: * Three months treatment of Vytorin 10/20mg will be superior to atorvastatin 20mg in ApoB/ApoA ratio. * In DM patients, Ezetimibe/Simvastatin Combination will be well-tolerated.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
132
simvastatin/ezetimibe 10/20mg once daily for 12weeks
atorvastatin 20mg once daily for 12weeks
Seoul national university hospital
Seoul, South Korea
change of ApoB/ApoA1
change of ApoB/ApoA1
Time frame: after 12 weeks' treatment
change of lipid profile
change of total cholesterol, LDL-cholesterol, HDL-cholesterol, Triglyceride, and APO B48
Time frame: 12weeks
change of HbA1c
change of HbA1c
Time frame: 12weeks
change of HOMA index
HOMA =\[Fasting insulin (mIU/L) × Fasting glucose (mmol/L)\] / 22.5
Time frame: 12weeks
change of hsCRP
change of hsCRP
Time frame: 12weeks
safety
CK elevation, Liver funtion test abnormality, and muscle realted adverse reactions and symptoms
Time frame: during 12weeks of treatment
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