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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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