Serum Salusin-β Levels Are Correlated with Slow Coronary Flow

被引:4
|
作者
Wang, Tao [1 ]
Dong, Ai-hua [2 ]
Cao, Hong-yun [3 ]
机构
[1] Shandong Jiaotong Hosp, Dept Cardiol, Jinan, Peoples R China
[2] Peoples Hosp Linzi Dist, Dept Cardiol, Zibo 255400, Shandong, Peoples R China
[3] Peoples Hosp Linzi Dist, Dept Clin Microbiol, 139 Huangong Rd, Zibo 255400, Shandong, Peoples R China
关键词
RECEPTOR-DEFICIENT MICE; BIOACTIVE PEPTIDES; ATHEROSCLEROSIS; EXPRESSION; DISEASE;
D O I
10.1089/gtmb.2015.0243
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Context: Slow coronary flow (SCF) is a special coronary microvascular disorder associated with recurrent chest pain. The pathogenesis of SCF remain unclear. Objectives: We sought to assess whether serum salusin-beta levels are correlated with SCF. Methods: We enrolled 76 patients with angiographically confirmed SCF and 108 age-and gender-matched controls. We measured serum salusin-beta levels by enzyme-linked immunosorbent assay and coronary flow rate was assessed using thrombolysis in myocardial infarction frame count (TFC). Results: Serum salusin-beta levels were elevated in SCF patients compared with controls (4.33 [range 3.52-5.87] nmol/L vs. 3.76 [range 2.98-4.67] nmol/L). Multivariate logistic regression analysis revealed that salusin-beta in serum was the independent predictor of SCF (odds ratio = 1.814). Serum salusin-beta levels were independently correlated with mean-TFC (r = 0.355, p = 0.002). Conclusions: Serum salusin-beta levels were independently associated with SCF. Therefore, our findings implicate a potential role of salusin-beta in the pathophysiology of SCF and provide insights on both risk stratification and modification in this patient population.
引用
收藏
页码:393 / 397
页数:5
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