Increased Plasma High-sensitivity C-reactive protein and Myeloperoxidase Levels May Predict Ischemia During Myocardial Perfusion Imaging in Slow Coronary Flow

被引:22
|
作者
Yurtdas, Mustafa [1 ]
Yaylali, Yalin Tolga [2 ]
Kaya, Yuksel [3 ]
Ozdemir, Mahmut [4 ]
机构
[1] Van Reg Training & Res Hosp, Dept Cardiol, Van, Turkey
[2] Pamukkale Univ, Sch Med, Dept Cardiol, Denizli, Turkey
[3] Kafkas Univ, Sch Med, Dept Cardiol, Kars, Turkey
[4] Ipekyolu State Hosp, Dept Cardiol, Van, Turkey
关键词
Coronary artery disease; Myocardial perfusion imaging; Coronary angiography; Inflammatory cardiovascular risk factors; AMERICAN-HEART-ASSOCIATION; HEALTH-CARE PROFESSIONALS; ENDOTHELIAL FUNCTION; DIFFUSE ATHEROSCLEROSIS; OXIDATIVE STRESS; ARTERY-DISEASE; INFLAMMATION; EXERCISE; MARKERS; HOMOCYSTEINE;
D O I
10.1016/j.arcmed.2013.10.019
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background and Aims. It is unclear whether changes in plasma levels of inflammatory markers could explain the link between ischemia and slow coronary flow (SCF). The aim of the study was to evaluate the plasma levels of high-sensitivity C-reactive protein (hsCRP), interleukin (IL)-6, and myeloperoxidase (MPO) during myocardial perfusion imaging (MPI) in SCF patients. Methods. The study population consisted of 53 SCF patients and 30 controls. Coronary flow rates were documented by TEVII frame count (TFC). Plasma levels of hsCRP, IL-6, MPO, and MPI were obtained in all participants. Results. hsCRP, IL-6 and MPO levels of SCF patients were higher than controls (hsCRP: 4.7 +/- 2.5 vs. 1.7 +/- 1.1 mg/L, p <0.001; IL-6: 8.2 +/- 4.3 vs. 5.2 +/- 2.1 pg/mL, p <0.001;. and MPO: 75.9 +/- 59.6 vs. 24.3 +/- 16.7 ng/mL, p <0.001). Twenty-one SCF patients exhibited myocardial perfusion defect (MPD) on MPI. In SCF patients, the highest hsCRP, IL-6 and MPO levels were observed in patients with both MPD and three-vessel slow flow. Mean TFCs were positively correlated with plasma levels of hsCRP (r = 0.424, p = 0.002), IL-6 (r = 0.367, p = 0.007), MPO (r = 0.430, p = 0.001), and reversibility score (r = 0.671, p <0.001) in SCF patients. HsCRP and MPO were the independent variables, which predicted positive MPI results (hsCRP: OR, 2.176; 95% CI, 1.200-3.943; p = 0.010, MPO: OR, 1.026; 95% CI, 1.007-1.046; p = 0.008). Conclusions. Inflammation may play a crucial role in both the pathogenesis and development of ischemia in SCF. Association of increased levels of inflammatory markers and ischemia suggests that endothelial inflammation may be largely responsible for clinical presentation. New combined treatment regimens should target endothelial activation and inflammation in SCF. (C) 2014 IMSS. Published by Elsevier Inc.
引用
收藏
页码:63 / 69
页数:7
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