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The Effect of Rosuvastatin 20 mg and Atorvastatin 40 mg on Plaque Regression and Stabilization in Patients with Mild to Moderate Degree of Coronary Stenosis with Vulnerable Plaque |
전남대학교병원 심장센터, 보건복지가족부 지정 심장질환 특성화 연구센터 |
홍영준, 정명호, 최윤하, 마은혜, 고점석, 이민구, 박근호, 심두선, 윤남식, 윤현주, 김계훈, 박형욱, 김주한, 안영근, 조정관, 박종춘, 강정채 |
Objectives: We used serial Intravascular ultrasound (IVUS) to assess the efficacy of rosuvastatin on plaque regression in angina patients with mild to moderate degree of vulnerable plaque burden.
Methods: This study was a prospective, randomized, comparative study for lipid lowering therapy using rosuvastatin 20 mg or atorvastatin 40 mg. IVUS was performed during baseline coronary angiography and repeated after 12-month of treatment. Efficacy parameters included changes in atheroma volume and the lipid pool size determined by IVUS. So far, a total of 68 patients were followed (rosuvastatin; 53 lesions in 38 patients vs. atorvastatin; 49 lesions in 30 patients).
Results: Low density lipoprotein (LDL)-cholesterol level was reduced from 130±37 mg/dL to 70±28 mg/dL in rosuvastatin group (a 46% decrease, p<0.001) and from 117±35 mg/dL to 76±24 mg/dL in atorvastatin group (a 35% decrease, p<0.001). Total atheroma and vessel volumes significantly decreased, whereas lumen volume significantly increased from baseline to follow-up in rosuvastatin and atorvastatin groups (△total atheroma volume; -5.25±8.95 mm3 vs. -3.31±6.78 mm3, p=0.223, △vessel volume; -3.79±12.3 mm3 vs. -3.20±9.01 mm3, p=0.784, △lumen volume; 1.45±8.63 mm3 vs. 0.70±5.54 mm3, p=0.605, △percent atheroma volume; -0.65±1.78% vs. -0.29±1.81%, p=0.314, respectively). Lipid pool size decreased more significantly in rosuvastatin group compared with atorvastatin group (△; -0.80±0.36 mm2 vs. -0.59±0.29 mm2, p=0.044). Follow-up LDL-cholesterol level correlated with change in total atheroma volume (r=0.327, p=0.001), change in percent atheroma volume (r=0.292, p=0.003), and change in lipid pool size (r=0.485, p=0.001).
Conclusions: Both rosuvastatin 20 mg and atorvastatin 40 mg could contribute to the regression of lipid-rich plaque, and LDL-cholesterol lowering is important in the regression and stabilization of the vulnerable coronary plaque.
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