Relationships of Elevated Systemic Pentraxin-3 Levels With High-Risk Coronary Plaque Components and Impaired Myocardial Perfusion After Percutaneous Coronary Intervention in Patients With ST-Elevation Acute Myocardial Infarction

被引:23
|
作者
Kimura, Shigeki [1 ]
Inagaki, Hiroshi [2 ]
Haraguchi, Go [3 ]
Sugiyama, Tomoyo [1 ]
Miyazaki, Toru [4 ]
Hatano, Yu [3 ]
Yoshikawa, Shunji [3 ]
Ashikaga, Takashi [3 ]
Isobe, Mitsuaki [3 ]
机构
[1] Yokosuka Kyosai Hosp, Ctr Cardiovasc, Yokosuka, Kanagawa 2388558, Japan
[2] Soka Municipal Hosp, Dept Cardiol, Soka, Japan
[3] Tokyo Med & Dent Univ, Dept Cardiovasc Med, Tokyo, Japan
[4] Kashiwa City Hosp, Dept Cardiol, Kashiwa, Chiba, Japan
关键词
Acute myocardial infarction; Atherosclerosis; Inflammation; Intravascular ultrasound; Perfusion; HISTOLOGY INTRAVASCULAR ULTRASOUND; C-REACTIVE PROTEIN; LONG PENTRAXIN; UNSTABLE ANGINA; PTX3; INFLAMMATION; CLASSIFICATION; MORPHOLOGY;
D O I
10.1253/circj.CJ-13-0329
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: We aimed to assess the relationships of pentraxin-3 (PTX3) with coronary plaque components and myocardial perfusion after percutaneous coronary intervention (PCI) in order to clarify the mechanisms underlying the prognostic function of PTX3 in ST-elevation acute myocardial infarction (STEMI) patients. Methods and Results: We enrolled 75 STEMI patients who underwent pre-PCI virtual histology (VH)-intravascular ultrasound. Relationships of the systemic pre-PCI PTX3 level with coronary plaque components and post-PCI myocardial blush grade (MBG) were evaluated. Lesions with elevated pre-PCI PTX3 (median >= 3.79 ng/ml) had higher frequencies of VH-derived thin-cap fibroatheroma (65.8% vs. 24.3%, P<0.0001), plaque rupture (63.2% vs. 24.3%, P=0.001), and post-PCI MBG (0-1) (65.8% vs. 40.5%, P=0.03) than those with PTX3 <3.79 ng/ml. In multivariate analysis, pre-PCI PTX3 level was independently related to post-PCI MBG (0-1) (odds ratio, 11.385; 95% confidence interval (Cl), 1.346-96.289; P=0.026). At 9-month follow-up, cardiac event-free survival was poorer for patients with post-PCI MBG (0-1) (log-rank test X-2=8.6; P=0.003). Cox proportional-hazards analysis showed post-PCI MBG (0-1) (hazard ratio, 4.109; 95% CI, 1.372-12.309; P=0.012) and Killip class >2 on admission (hazard ratio, 5.356; 95% Cl, 1.409-20.359; P=0.014) as independent predictors of adverse cardiac events during follow-up. Conclusions: Systemic pre-PCI PTX3 was associated with high-risk plaque components and impaired post-PCI myocardial perfusion. Thus, PTX3 may be a reliable predictor of outcome in STEMI patients.
引用
收藏
页码:159 / 169
页数:11
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