Kai H, Ikeda H, Yasukawa H, Kai M, Seki Y, Kuwahara F, Ueno T, Sugi K, Imaizumi T
Third Department of Internal Medicine and the Cardiovascular Research Institute, Kurume University School of Medicine, Fukuoka, Japan.
J Am Coll Cardiol. 1998 Aug;32(2):368-72. doi: 10.1016/s0735-1097(98)00250-2.
This study was sought to investigate whether peripheral blood levels of matrix metalloproteases (MMPs) are affected in patients with acute coronary syndromes (ACS).
Synthesis of MMPs has been reported in coronary atherosclerotic lesions in patients with unstable angina (UA), suggesting a pathogenic role of MMPs in the development of ACS.
Using sandwich enzyme immunoassay, serum MMP-2 and plasma MMP-9 were measured in 33 patients with ACS (22 with acute myocardial infarction [AMI], 11 with UA), 17 with stable effort angina (EA) and 17 normal control subjects.
Serum MMP-2 in patients with UA and AMI on day 0 was two times greater than that in control subjects, and patients with EA showed higher MMP-2 levels than those in control subjects. Plasma MMP-9 in patients with UA and AMI on day 0 was elevated by threefold and twofold versus that in control subjects, respectively. In patients with UA and AMI who underwent medical treatment (n = 11 and 13, respectively), MMP-2 elevation was sustained until day 7. In patients with UA, MMP-9 elevation on day 0 was followed by a gradual decrease toward the control range up to day 7. Some patients with AMI showed a transient MMP-9 elevation with a peak on day 3, whereas in others, MMP-9 levels were significantly elevated on day 0 and remained higher than those in control subjects up to day 3.
Serial changes in serum MMP-2 and plasma MMP-9 were documented in patients with ACS. These findings provide an insight into the molecular mechanism of plaque destabilization.
本研究旨在调查急性冠脉综合征(ACS)患者外周血基质金属蛋白酶(MMPs)水平是否受到影响。
已有报道称不稳定型心绞痛(UA)患者的冠状动脉粥样硬化病变中有MMPs的合成,提示MMPs在ACS的发生发展中起致病作用。
采用夹心酶免疫测定法,检测了33例ACS患者(22例急性心肌梗死[AMI],11例UA)、17例稳定劳力性心绞痛(EA)患者和17例正常对照者的血清MMP-2和血浆MMP-9水平。
UA和AMI患者第0天的血清MMP-2水平是对照者的两倍,EA患者的MMP-2水平高于对照者。UA和AMI患者第0天的血浆MMP-9水平分别比对照者升高了3倍和2倍。接受药物治疗的UA和AMI患者(分别为11例和13例),MMP-2升高持续至第7天。UA患者中,第0天MMP-9升高后,直至第7天逐渐降至对照范围。部分AMI患者MMP-9出现短暂升高,第3天达到峰值,而其他患者MMP-9水平在第0天显著升高,并在第3天前一直高于对照者。
记录了ACS患者血清MMP-2和血浆MMP-9的系列变化。这些发现为斑块不稳定的分子机制提供了见解。