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Dose-dependent INhibitory effect of rosuVastatin In Japanese patienTs with Acute myocardial infarcTION on serum concentration of matrix metalloproteinases - INVITATION trial

Authors :
Kazuteru Fujimoto
Seiji Hokimoto
Kenji Sakamoto
Koichi Kaikita
Yasuhiro Nagayoshi
Ichiro Kajiwara
Natsuki Nakamura
Eiichiro Yamamoto
Invitation study investigators
Toyoki Hirose
Koichi Nakao
Shinichi Nakamura
Koichiro Fujisue
Tomohiro Sakamoto
Shuichi Oshima
Takuhiro Shirakawa
Shinji Tayama
Jun Hokamaki
Naritsugu Sakaino
Nobutaka Hirai
Yasuhiro Izumiya
Hideki Maruyama
Ryusuke Tsunoda
Hideki Shimomura
Hisao Ogawa
Toshiyuki Matsumura
Nobuyasu Yamamoto
Kenichi Tsujita
Source :
Journal of cardiology. 72(4)
Publication Year :
2017

Abstract

Background Acute myocardial infarction (AMI) is mainly characterized by the rupture of lipid-rich vulnerable atherosclerotic plaque. The matrix metalloproteinases (MMPs) have been shown to play a critical role in inflammatory processes underlying plaque rupture. Some reports suggested statins inhibit the increased MMP levels after AMI. However, there are a few comparison studies between the different dosages of the same statin and circulating levels of MMPs. Purpose This study will preliminarily investigate the potential effects of appropriate or low dose of rosuvastatin on circulating MMPs levels in AMI patients. Moreover, we will also obtain plasma from patients while undergoing diagnostic angiography to determine differences in various cardiac sites and peripheral vessels. Methods This study is a multicenter, open-label, randomized, parallel-group study to be conducted to compare the appropriate or low dose of rosuvastatin in the effect on serum levels of inflammatory markers in AMI patients. The eligible patients undergoing percutaneous coronary intervention (PCI) will be randomly assigned to receive either appropriate or low-dose rosuvastatin daily using a web-based randomization software within 24 h after PCI. The low-dose group will be treated with rosuvastatin 2.5 mg once daily with a follow-up. The appropriate-dose group will begin treatment with rosuvastatin 5 mg once daily, and the dose of rosuvastatin will be titrated to 10 mg within 4 weeks. During administration of the study treatment, subjects will undergo laboratory testing including MMPs and be monitored for the occurrence of adverse events up to 24 weeks. The primary endpoint will be the change rate of MMPs at 24 weeks after administration. Conclusions INVITATION will compare the appropriate or low dose of rosuvastatin in the effects on serum levels of inflammatory markers including MMPs in AMI patients. This study will provide significant information on rosuvastatin as an anti-inflammatory agent for AMI.

Details

ISSN :
18764738
Volume :
72
Issue :
4
Database :
OpenAIRE
Journal :
Journal of cardiology
Accession number :
edsair.doi.dedup.....839bffe4310046257ee310e3321093fc