Background
Coronary atherosclerosis is a complex, long lasting and continuously evolving inflammatory disease [
1]. Acute myocardial infarction (AMI) is an acute event of coronary atherosclerosis with a process involved with multiple inflammatory factors [
2]. Visfatin is a novel adipokine found in 2005 by Fukuhara et al. [
3]. Studies have demonstrated serum visfatin levels correlated with the presence of inflammatory state [
4]. Visfatin may induce the secretion of the pro-inflammatory cytokines and could contribute to systemic and plaque inflammation in atherosclerotic disorders through impacting macrophages [
5,
6]. Visfatin was found to be abundant in foam cells of unstable atherosclerotic plaques in AMI, and relevant to the destabilization of atherosclerotic plaque [
7].
Previous studies have shown that visfatin was significantly increased in coronary atherosclerosis disease (CAD), and might be a promising biomarker for the diagnosis of CAD [
8‐
11]. However, its relationship with the occurrence of severe coronary events remains unclear. Therefore, in this study, we sought to explore the association between serum visfatin levels and major adverse cardiovascular events (MACEs) in AMI.
Methods
Study population
A total of 238 Chinese patients, who received coronary angiography in the department of cardiology in Fujian Provincial Hospital from January 2016 to September 2016 were recruited for this study. AMI group (
N = 183, 62 ST-segment elevation myocardial infarction and 121 Non-ST segment elevation myocardial infarction) was defined with more than 50% stenosis in coronary arteries and positive troponin. The diagnostic criteria of AMI adopted the American College of Cardiology (ACC)/American Heart Association (AHA)/World Heart Federation (WHF)/European Society of Cardiology (ESC) guidelines established in 2012 [
12]. Control group (
N = 55) was defined with less than 50% stenosis in coronary arteries and negative troponin. The exclusion criteria as follows: valvular heart disease, myocarditis, cardiomyopathy, hypohepatia, thyroid dysfunction, end-stage chronic kidney disease, malignancy and hematological system diseases. The study complied with the Declaration of Helsinki and was approved by the ethical committee of Fujian Provincial Hospital (K2016–01-001) (
supplemental materials). Each participant provided written, informed consent before enrollment.
Patient information (such as age, gender, body mass index, hypertension, diabetes, hyperlipidemia, history of myocardial infarction and smoking) was recorded by standardized form. The cardiac biomarkers (cardiac troponin-I, N-terminal pro-brain natriuretic peptide) and thrombin index (fibrinogen, D-dimer) were detected immediately after admission. Other vein biochemical index were detected in the next morning (fasting for 8–12 h) after admission, including glucose, albumin, creatinine, triglycerides, total cholesterol, high-density lipoprotein, low-density lipoprotein, apolipoprotein-a, apolipoprotein-b. The above indicators were completed by the laboratory department of our hospital and we obtain laboratory parameter from the patients medical records at index admission.
Visfatin detection
Blood samples were collected into EDTA-containing tubes from subjects at baseline at least 8–12 h fasting before coronary angiography and centrifuged at 700 g. Serum concentration of visfatin was determined by enzyme-linked immunosorbent assay with the EK-003-80 human visfatin kit (Phoenix Pharmaceuticals, Belmont, CA). The operation steps followed the instructions strictly.
Coronary angiography
Standard Judkins technique was carried out in the coronary arteriography and all coronary artery stenosis was imaged from multiple projections. Two expert cardiologists who were blinded to the patients’ clinical and laboratory data reviewed the coronary angiography and evaluated the coronary atherosclerotic lesion severity independently. According to the number of stenosis which was detected ≥50% of the lumen diameter of a coronary artery, we divided it into single-vessel lesion, double vessel lesion and multi-vessel lesion.
Follow-up
In this study, all of AMI patients were followed up after admission using a standardized protocol that included outpatient follow up, telephone contacts and hospital data. The endpoints was MACEs, including death of cardiovascular events, nonfatal myocardial infarction (re-MI), target lesion revascularization (percutaneous coronary intervention or coronary artery bypass graft) and re-admission due to advanced heart failure.
Statistical analysis
The version 22.0 SPSS software suite was used for all statistical analyses. Continuous variables was tested for normality test. Normally distributed data was expressed as mean ± standard deviation and skewed distributions data was expressed as median with inter-quartile range. Intergroup comparisons of clinical data were performed with student’s t-test (normally distributed data) or the Mann–Whitney U test (skewed data). Multiple groups comparisons of clinical data were performed with the analysis of variance (normally distributed data) or the Kruskal-Wallis H test (skewed data). Categorical variables were presented as number (percentage) and analyzed by chi-square statistic test. Binary Logistic regression was used to analyze the factors which were correlated with the occurrence of MACEs in a stepwise backward conditional manner. Receiver-operating characteristic (ROC) curves was used to evaluated the predictive value of visfatin for the occurrence of MACEs. Cox regression analysis was used to analyze the factors which were correlated with the time to MACEs and Kaplan-Meier curves was used to estimate the survival time between high and low visfatin group with a log-rank test. For all analyses, two tailed P values < 0.05 were.
Discussion
In the present study, we found that serum visfatin level was elevated in AMI patients and contributed to MACEs incidence. Visfatin, total cholesterol, LDL-C and diabetes were correlated with the occurrence of MACEs in AMI patients. A combined model consisting of visfatin and traditional risk factors showd a higher specificity in predicting MACEs. The occurrence of MACEs was elevated in high-visfatin group, especially in non-fatal re-MI. Visfatin was correlated with the onset to MACEs and high serum visfatin level was associated with an earlier onset of MACEs.
Visfatin (also referred as Pre-B cell colony enhancing factor and nicotinamide phosphoribosyltransferase) is a member of adipokine with a molecular weight about 52kD [
13]. Studies have demonstrated that visfatin could promote insulin and pro-inflammatory cytokines secretions [
5,
14], and it is a pleiotropic protein implicated in the pathophysiology of obesity, metabolic disease, diabetes and cancer [
15‐
18]. Dahl et al. firstly reported that visfatin was markedly enhanced in symptomatic carotid atherosclerotic plaques [
19]. Subsequently, various studies provided that visfatin was closely related with cardiovascular disease [
20‐
26]. Horbal et al. showd that the odds of severe hypertension were in accordance with the levels of visfatin [
21]. Bobbert et al. discovered high visfatin in nonischemic dilated congestive cardiomyopathy (DCM) patients was associated with a favorable outcome and improvement in functional status [
22]. In addition, serum visfatin level was observed to be significantly higher in premature coronary artery disease and coronary slow flow (CSF) [
23,
24]. Notably, an augmented level of visfatin in STEMI was positively correlated with the number of coronary lesions [
10,
25]. We also found an increase of serum visfatin levelin AMI patients. However, there was no statistically significant difference in the number of coronary lesions, possibly because of the limited number of subjects in our study.
In this study, an average of 19.3 months of follow-up was conducted for 159 patients with AMI. A total of 18 (11.32%) patients had MACEs in follow-up, among those, 7 (4.40%) suffered non-fatal re-MI, 2 (1.26%) suffered heart failure, 9 (5.65%) were dead of cardiovascular events. Binary logistic analysis showed that visfatin, total cholesterol, LDL-C and diabetes were all associated with the occurrence of MACEs.
We applied ROC curves to evaluate the contribution of traditional risk factors (smoking, hypertension, diabetes, hyperlipidemia and body mass index) and visfatin in predicting MACEs. We discovered that visfatin and traditional risk factors had a specificity of 68.8 and 66.7% in predicting MACEs,respectively, while a combined model consisting of all factors showed a 73.8% specificity. The combined model greatly improved the predictive of MACEs and clinical practical value. Our data showed the occurrence of MACEs was elevated in high-visfatin group, especially in non-fatal re-MI.
Multivariate Cox proportional hazards regression analysis suggested that visfatin was correlated with the onset to MACEs. Kaplan-Meier curves demonstrated that the onset to MACEs was earlier in high-visfatin group compared with low-visfatin group, and the cumulative survival time was shorter. Although the mechanisms of visfatin in coronary atherosclerotic heart disease remain unclear, previous researchers had shown the increased serum visfatin level after drug-eluting stents (DES) placement was independently associated with in-stent restenosis (ISR) [
26]. Visfatin could promote the production of interleukin (IL)-6 and intercellular adhesion molecule-1 (ICAM-1) and regulate nuclear factor (NF)-kappaB, which resulted in the apoptosis of endothelial progenitor cells (EPCs) [
5]. Visfatin could also increase the expression of metal matrix proteinase (MMP)-8 in macrophages, promote collagen degradation and the plaques vulnerability index [
27]. Visfatin was indicated to be abundant in foam cells within unstable atherosclerotic plaques [
7]. Therefore, we presume visfatin may contribute to the MACEs by regulating the inflammation, apoptosis and collagen degradation, and we will take further clinical research and basic experimental to investigate the possible mechanism behind.
There were several limitations in the present study. First, the subjects recruited were hospitalized in single centre, lacking regional and ethnic comparisons. Second, the sample size was limited and the follow-up time was relatively short. Third, lacking of dynamic monitoring of visfatin levels during the follow-up period.
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