Endothelial Function and Pro-Inflammatory Cytokines as Prognostic Markers in Acute Coronary Syndromes

被引:0
作者
Tsalamandris, Sotirios [1 ]
Koliastasis, Leonidas [1 ]
Miliou, Antigoni [1 ]
Oikonomou, Evangelos [2 ]
Papageorgiou, Nikos [1 ]
Antonopoulos, Alexis [1 ]
Hatzis, George [1 ]
Mourouzis, Konstantinos [2 ]
Vogiatzi, Georgia [1 ]
Siasos, Gerasimos [2 ]
Xaplanteris, Panagiotis [3 ]
Tousoulis, Dimitris [1 ]
机构
[1] Natl & Kapodistrian Univ Athens, Hippokrat Gen Hosp, Sch Med, Dept Cardiol 1, Athens 11527, Greece
[2] Natl & Kapodistrian Univ Athens, Sotiria Chest Dis Hosp, Med Sch, Dept Cardiol 3, Athens 11527, Greece
[3] Univ Libre Bruxelles ULB, Ctr Hosp Univ St Pierre, Dept Cardiol, B-1000 Brussels, Belgium
关键词
acute coronary syndrome; coronary artery disease; endothelial function; inflammation; pro-inflammatory cytokines; MYOCARDIAL-INFARCTION; ARTERY-DISEASE; SHEAR-STRESS; RISK; ATHEROSCLEROSIS; INTERLEUKIN-1; PLAQUE;
D O I
10.3390/diagnostics15081033
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Endothelial dysfunction and inflammation are associated with the progression of coronary artery disease (CAD) and the pathophysiology of acute coronary syndrome (ACS). We examined the prognostic role of endothelial function and pro-inflammatory cytokines in patients admitted with ACS. Methods: The study population consisted of 864 subjects. From 663 subjects who presented with chest pain, ACS was diagnosed in 460. We additionally recruited 201 consecutive patients with stable CAD. Endothelial function was assessed using flow-mediated dilatation (FMD). Tumor necrosis factor alpha (TNF-alpha) and interleukin-6 (IL-6) levels were measured via ELISA. Subjects with ACS were followed up for major adverse cardiovascular events (MACE), defined as cardiovascular death, cardiac arrest, myocardial infarction, stroke, nonfatal stroke, other arterial thrombotic events, and hospitalization due to cardiovascular conditions. Results: There was a stepwise impairment in FMD, logTNF-alpha, and logIL-6 in patients with chest pain of non-epicardial CAD etiology compared to patients with stable CAD and those with ACS (p < 0.001 for all). Moreover, patients who presented with chest pain had increased odds of ACS in accordance with the increasing levels of TNF-alpha, IL-6, and impaired FMD (p < 0.05 for all). Interestingly, from all these markers, in patients with ACS, we found that only TNF-alpha levels above 5.19 pg/mL had a 2.5-times-increased risk of MACE compared to patients with TNF-alpha levels below 5.19 pg/mL, independently of other confounders. Conclusions: In the current study, we found that patients who presented with ACS had impaired endothelial function and increased levels of IL-6 and TNF-alpha.
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