TY - JOUR
T1 - Effects of ezetimibe-statin combination therapy on coronary atherosclerosis in acute coronary syndrome
AU - Ezetimibe-ACS Investigators
AU - Hibi, Kiyoshi
AU - Sonoda, Shinjo
AU - Kawasaki, Masanori
AU - Otsuji, Yutaka
AU - Murohara, Toyoaki
AU - Ishii, Hideki
AU - Sato, Katsuhiko
AU - Koshida, Ryoji
AU - Ozaki, Yukio
AU - Sata, Masataka
AU - Morino, Yoshihiro
AU - Miyamoto, Tadashi
AU - Amano, Tetsuya
AU - Morita, Satoshi
AU - Kozuma, Ken
AU - Kimura, Kazuo
AU - Fujiwara, Hisayoshi
N1 - Publisher Copyright:
© 2018, Japanese Circulation Society. All rights reserved.
PY - 2018
Y1 - 2018
N2 - Background: The results of previous clinical trials on the effects of ezetimibe-statin combination therapy on atherosclerosis are inconsistent, and the anti-atherosclerotic effect of ezetimibe remains controversial. Methods and Results: We conducted a prospective, randomized open-label study at 10 centers. One hundred and twenty-eight statin-naïve patients with acute coronary syndrome (ACS) undergoing intravascular ultrasound (IVUS)-guided percutaneous coronary intervention were randomized to receive either 2 mg/day pitavastatin plus 10 mg/day ezetimibe, or 2 mg/day pitavastatin. One hundred and 3 patients had evaluable IVUS of non-culprit coronary lesions at baseline and at follow-up. The primary endpoint was the percentage change in non-culprit coronary plaque volume (PV) and lipid PV on integrated backscatter IVUS. Mean low-density lipoprotein cholesterol was reduced from 123 mg/dL to 64 mg/dL in the combination therapy group (n=50) and 126 mg/dL to 87 mg/dL in the statin alone group (n=53; between-group difference, 16.9%, P<0.0001). The percent change in PV was −5.1% in the combination therapy group and −6.2% in the statin alone group (P=0.66), although both groups had reduction of PV compared with baseline (both P<0.01). The percent change in lipid PV did not differ between the groups (4.3 vs. −3.0%, P=0.37). Conclusions: In statin-naïve patients with ACS, combined therapy with ezetimibe and statin did not result in a significant change in coronary plaque regression or tissue component compared with statin alone.
AB - Background: The results of previous clinical trials on the effects of ezetimibe-statin combination therapy on atherosclerosis are inconsistent, and the anti-atherosclerotic effect of ezetimibe remains controversial. Methods and Results: We conducted a prospective, randomized open-label study at 10 centers. One hundred and twenty-eight statin-naïve patients with acute coronary syndrome (ACS) undergoing intravascular ultrasound (IVUS)-guided percutaneous coronary intervention were randomized to receive either 2 mg/day pitavastatin plus 10 mg/day ezetimibe, or 2 mg/day pitavastatin. One hundred and 3 patients had evaluable IVUS of non-culprit coronary lesions at baseline and at follow-up. The primary endpoint was the percentage change in non-culprit coronary plaque volume (PV) and lipid PV on integrated backscatter IVUS. Mean low-density lipoprotein cholesterol was reduced from 123 mg/dL to 64 mg/dL in the combination therapy group (n=50) and 126 mg/dL to 87 mg/dL in the statin alone group (n=53; between-group difference, 16.9%, P<0.0001). The percent change in PV was −5.1% in the combination therapy group and −6.2% in the statin alone group (P=0.66), although both groups had reduction of PV compared with baseline (both P<0.01). The percent change in lipid PV did not differ between the groups (4.3 vs. −3.0%, P=0.37). Conclusions: In statin-naïve patients with ACS, combined therapy with ezetimibe and statin did not result in a significant change in coronary plaque regression or tissue component compared with statin alone.
KW - Acute coronary syndrome
KW - Intravascular ultrasound
KW - Lipid-lowering therapy
KW - Low-density lipoprotein cholesterol
UR - http://www.scopus.com/inward/record.url?scp=85042510747&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85042510747&partnerID=8YFLogxK
U2 - 10.1253/circj.CJ-17-0598
DO - 10.1253/circj.CJ-17-0598
M3 - Article
C2 - 29212965
AN - SCOPUS:85042510747
SN - 1346-9843
VL - 82
SP - 757
EP - 766
JO - Circulation Journal
JF - Circulation Journal
IS - 3
ER -