Plasma angiopoietin-1 level, left ventricular ejection fraction, and multivessel disease predict development of 1-year major adverse cardiovascular events in patients with acute ST elevation myocardial infarction - A pilot study

被引:17
作者
Liu, Kuan-Liang [1 ]
Lin, Shu-Min [2 ]
Chang, Chih-Hsiang [3 ]
Chen, Yung-Chang [3 ]
Chu, Pao-Hsien [1 ,4 ,5 ]
机构
[1] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Dept Internal Med,Div Cardiol, Taipei 105, Taiwan
[2] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Dept Thorac Med, Taipei 105, Taiwan
[3] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Dept Nephrol, Taipei 105, Taiwan
[4] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Healthcare Ctr, Taipei 105, Taiwan
[5] Chang Gung Univ, Chang Gung Mem Hosp, Coll Med, Heart Failure Ctr, Taipei 105, Taiwan
关键词
Angiopoietin; Acute myocardial infarction; Multivessel disease; Major cardiovascular events; ENDOTHELIAL DYSFUNCTION; MORTALITY; THROMBOMODULIN; INFLAMMATION; BALANCE; STROKE; IMPACT; INJURY; CELLS; RISK;
D O I
10.1016/j.ijcard.2014.12.172
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Patients with acute myocardial infarction (AMI) are frequently complicated with major cardiovascular events (MACEs). Endothelial dysfunction has been found to be involved in pathogenesis of AMI, but its role in development of MACEs after AMI is not clearly investigated. This study aimed to determine whether the plasma markers of endothelial dysfunction could serve as independent predictors for MACEs in patients with AMI. Methods: This prospective study was conducted from March 2010 to July 2012 and enrolled consecutive 132 patients with acute ST elevation myocardial infarction (STEMI) receiving primary percutaneous coronary intervention (PCI). Plasma levels of thrombomodulin (TM), von Willebrand factor (vWF), angiopoietin (Ang)-1, Ang-2, Tie-2, and vascular endothelial growth factor (VEGF) were measured on day 1 of AMI. The development of MACEs at 1-year follow-up was recorded. Result: Patients with STEMI who developed MACEs had increased heart rate on admission (86 +/- 24 vs. 74 +/- 20 bpm, p = 0.006), lower left ventricular ejection fraction (LVEF) (49.0 +/- 12.4 vs. 57.2 +/- 12.4%, p = 0.002), and higher incidence of multivessel disease (66.7% vs. 42.2%, p = 0.018) comparing with those without MACEs. Plasma level of Ang-1 was lower in patients with MACEs than in those without (21,165 +/- 16,281 vs. 31,411 +/- 21,593 pg/mL, p = 0.018). In multivariate analysis, Ang-1 level < median value (OR 2.977, 95% CI 1.16-7.63, p = 0.023), LVEF (OR 0.958, 95% CI 0.92-0.99, p = 0.022) and multivessel disease (OR 3.013, 95% CI 1.19-7.60, p = 0.019) independently predicted 1-year MACEs. Conclusion: Decreased plasma Ang-1 levels on admission, LVEF and multivessel disease independently predicted the development of 1-year MACEs in patients with STEMI. These results suggest that endothelial dysfunction may play an important role in mediating MACEs in patients with STEMI. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:155 / 160
页数:6
相关论文
共 31 条
[1]   Impact of coronary artery stents on mortality and nonfatal myocardial infarction: Meta-analysis of randomized trials comparing a strategy of routine stenting with that of balloon angioplasty [J].
Al Suwaidi, J ;
Holmes, DR ;
Salam, AM ;
Lennon, R ;
Berger, PB .
AMERICAN HEART JOURNAL, 2004, 147 (05) :815-822
[2]   Tie2 receptor ligands, angiopoietin-1 and angiopoietin-2, modulate VEGF-induced postnatal neovascularization [J].
Asahara, T ;
Chen, DH ;
Takahashi, T ;
Fujikawa, K ;
Kearney, M ;
Magner, M ;
Yancopoulos, GD ;
Isner, JM .
CIRCULATION RESEARCH, 1998, 83 (03) :233-240
[3]   Control of vascular morphogenesis and homeostasis through the angiopoietin-Tie system [J].
Augustin, Hellmut G. ;
Koh, Gou Young ;
Thurston, Gavin ;
Alitalo, Kari .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2009, 10 (03) :165-177
[4]   Promoter variant of angiopoietin-2 and plasma angiopoietin-2 are associated with risk of stroke recurrence in lacunar infarct patients [J].
Chen, Jingzhou ;
Yu, Hui ;
Sun, Kai ;
Song, Weihua ;
Bai, Yongyi ;
Yang, Tao ;
Song, Yan ;
Zhang, Yinhui ;
Hui, Rutai .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 398 (02) :212-216
[5]   Angiogenesis as Risk Factor for Plaque Vulnerability [J].
Di Stefano, Rossella ;
Felice, Francesca ;
Balbarini, Alberto .
CURRENT PHARMACEUTICAL DESIGN, 2009, 15 (10) :1095-1106
[6]   The relative importance of vascular structure and function in predicting cardiovascular events [J].
Fathi, R ;
Haluska, B ;
Isbel, N ;
Short, L ;
Marwick, TH .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2004, 43 (04) :616-623
[7]   Angiopoietin-2 sensitizes endothelial cells to TNF-α and has a crucial role in the induction of inflammation [J].
Fiedler, U ;
Reiss, Y ;
Scharpfenecker, M ;
Grunow, V ;
Koidl, S ;
Thurston, G ;
Gale, NW ;
Witzenrath, M ;
Rosseau, S ;
Suttorp, N ;
Sobke, A ;
Herrmann, M ;
Preissner, KT ;
Vajkoczy, P ;
Augustin, HG .
NATURE MEDICINE, 2006, 12 (02) :235-239
[8]   Circulating angiopoietin 2 correlates with mortality in a surgical population with acute lung injury/adult respiratory distress syndrome [J].
Gallagher, Diana C. ;
Parikh, Samir M. ;
Balonov, Konstantin ;
Miller, Andrew ;
Gautam, Shiva ;
Talmor, Daniel ;
Sukhatme, Vikas P. .
SHOCK, 2008, 29 (06) :656-661
[9]  
Hong Young Joon, 2003, J Interv Cardiol, V16, P209, DOI 10.1034/j.1600-0854.2003.8048.x
[10]   Decreased heparin cofactor II activity is associated with impaired endothelial function determined by brachial ultrasonography and predicts cardiovascular events [J].
Huang, Po-Hsun ;
Leu, Hsin-Bang ;
Chen, Jaw-Wen ;
Wu, Tao-Cheng ;
Lu, Tse-Min ;
Ding, Philip Yu-An ;
Lin, Shing-Jong .
INTERNATIONAL JOURNAL OF CARDIOLOGY, 2007, 114 (02) :152-158