Background
Complement C1q tumor necrosis factor related proteins (CTRPs) superfamily is a cluster of adipokines, currently, 15 members are identified [
1]. The highly conserved family of proteins share a similar modular organization to adiponectin and contain four distinct domains [
2]. The members of CTRPs participate in the regulation of physiological and pathological processes, such as glucose and lipid metabolism, inflammation, myocardial protection, vasodilatation. CTRP 1 is identified as an adipokine, its expression is greatly increased in adipose tissue of
db/db mice and Zucker diabetic fatty
(fa/fa) rats [
3]. It has been reported that the levels of CTRP 1 were significantly up-regulated in hypertensive patients’ serum [
4]. Furthermore, CTRP 1 prevents collagen-induced platelet aggregation by specific blockade of von Willebrand’s factor binding to collagen, which suggests that CTRP 1 could be acted as a potent antithrombotic factor [
5]. A recent study revealed that serum CTRP 1 levels were significantly increased in patients with type 2 diabetes mellitus, CTRP 1 was a novel adipokine associated with type 2 diabetes mellitus in humans [
6]. The study by Shen and her colleagues [
7] demonstrated that CTRP 1 could inhibit in vitro angiogenesis of endothelial progenitor cells from patients with severe coronary artery disease.
Coronary artery disease (CAD) is one of the most prevalent cardiovascular diseases, it is a group of diseases that included: stable angina, unstable angina, myocardial infarction, and sudden coronary death [
8]. In 2013, CAD was the most common cause of death globally [
9]. Multiple risk factors for CAD have been identified, including smoking, family history, hypertension, obesity, diabetes, lack of exercise, stress, and high blood lipids [
10]. CTRP has also been shown to have diverse biological influences on cardiovascular system [
7]. Pervious observations showed that CTRP 1 is associated with metabolic and vascular disorders, and those disorders are contributed to the pathogenesis of angiocardiopathy.
Among the extensive researches on the pathogenesis of cardiovascular disease, the role of adipokines has been gradually drawn more and more researchers’ attention [
11]. Adipose tissue is not only considered as energy tissue, but also as an important endocrine organ that derives a number of biologically active adipokines. These adipokines exert the extraordinary biological functions. CTRP 1 is a member of the CTRP superfamily and express at high levels in adipose tissues. But there were little research explored the relevance of CTRP 1 with CAD. Hence, we developed a study regarding CTRP 1 and its relation with the prevalence or severity of CAD.
Methods
Subjects
A total of 200 participants who have underwent coronary angiography successfully at the Department of Cardiology, The 305 Hospital of the People’s Liberation Army were enrolled in the study between January 2010 and January 2012. The subjects included 133 males and 67 females, the average age was 61.11 ± 11.83 years. Stable and unstable angina pectoris were determined by American College of Cardiology (ACC)/American Heart Association (AHA) 2007 guidelines [
12], the diagnosis of acute myocardial infarction was performed according to the clinical history, electrocardiogram and serum myocardial enzymogram. With the reference of their clinical diagnosis and coronary angiography results, they were divided into CAD group (
n = 150) and non-CAD group (
n = 50, with normal coronary artery angiogram). And CAD group further grouped into 3 subgroups by their clinical course: stable angina (SA) group (
n = 48), unstable angina (UA) group (
n = 43) and acute myocardial infarction (AMI) group (
n = 59). The participants with cerebral infarction, thrombotic diseases, valvular heart disease, severe hepatic and renal dysfunction, tumors, infections and hematologic disorders were excluded. All of them were given written informed consent. This study was approved by the ethics committee of The 305 Hospital of the People’s Liberation Army.
Methods
Blood samples were obtained within 24 h of admission from all the participants. Peripheral venous blood cells were isolated by density gradient centrifugation and the serum was stored at −70 °C. CTRP 1 levels were determined quantitatively with enzyme-linked immunosorbent assay using the commercially available ELISA kit (Cloud-Clone Corp) and followed the manufacturer’s recommendations. Other serum indexes were measured by routine methods using a fully automatic biochemical analyzer (UniCel DxC 800 Synchron, Beckman Coulter, Inc., USA).
The Seldinger technique was used in the coronary angiography. A GE300 cardiovascular angiographic system was used to show lesion location. According to different parts involved, the lesion can be classified into left main, anterior descending, circumflex and right coronary artery lesion. A stenosis ≥ 50 % was considered as CAD, and left main stenosis ≥ 50 % was considered as double-vessel disease.
Statistical analysis
Statistical analyses were performed using SPSS 17.0 software. The measurement data were conducted by normality test. Continuous variables were presented as mean ± standard deviation (SD). The difference of measurement data was compared with t test between groups. Tukey’s test was used for pairwise comparison between groups. Count data were assessed using chi-square test. Logistic regression analysis was used to identify the association between CAD and other variables. All statistical tests used a P value of 0.05 in a two-tailed test as statistically significant.
Discussion
Our study demonstrated that the CTRP 1 levels were increased in patients with CAD compared to non-CAD subjects, and the CTRP 1 levels were on an upward trend with the progress of disease. Multiple logistic regression analysis showed that increased CTRP 1 level was independent risk factor of myocardial infarction.
Some studies have indicated that CTRP family members, including adiponectin, CTRP 3 and CTRP 9, were involved in the regulation of cardiovascular disease in mice and human. For example, CTRP 3 has been found to be associated with cardiac risk factors in human [
13]. Yi [
14] first demonstrated that the expression and production of CTRP 3 were significantly reduced after myocardial infarction, the administration of CTRP 3 could improve survival rate and restore cardiac function in mice with coronary artery occlusion. Animal experiments showed that CTRP 9 administration to mice significantly reduced infarct size and improved cardiac function [
15], and CTRP 9 protected against acute cardiac injury following ischemia-reperfusion via an AMPK-dependent mechanism [
16]. Furthermore, CTRP 9 was also a vasorelaxative adipocytokine that exerted vasculoprotective effects [
17].
In recent study, increased serum CTRP 1 level in SA patients were observed [
7]. Consistent with these findings, our data in this study indicated that CTRP 1 levels in CAD group were significantly higher than non-CAD group. It has also been reported that CTRP 1 levels were elevated with the disease progresses and coronary lesion vessels. All these observations proved that CTRP 1 level were closely related to the pathogenesis and severity of CAD. Previous studies have reported that CTPR 1 were significantly increased in subjects with hypertension [
4], diabetes [
6], as well as metabolic syndrome [
18]. Because these diseases were the recognized risk factors for atherosclerosis, in order to test whether our findings were influenced by those factors, multivariate stepwise regression analysis was performed to evaluate the independent factors of myocardial infarction with the above factors. Gender, glucose and CTRP 1 were the independent risk factors. It was obvious that metabolic abnormalities induced by CAD affected CTRP 1 levels more or less, but the increased CTRP 1 levels probably not related to them completely. The body’s inflammatory states and mutual adjustment between other members in CTRP superfamily might also contribute the enhancement of CTRP 1.
Conclusion
The actual role of CTRP 1 in the cardiovascular system is completely unknown [
19]. However, the increased CTRP 1 were closed related with CAD, suggesting CTRP1 levels might serve as a predictor of CAD. Therefore, CTRP 1 levels in CAD patients should be paid highly attentions. There were important potential for CTRP 1 to be used as a novel biomarker to evaluate cardiovascular risk, but the assumption needed future clarification after acquiring the exact mechanism. The future study should conduct on a larger population, and potential confounding factors such as obesity should be excluded. Meanwhile, as a member of complex CTRP family, the interrelationship of other members with different biological function should be considered.
Ethics approval and consent to participate
This study was approved by the ethics committee of The 305 Hospital of the People’s Liberation Army. All of participants were given written informed consent.
Availability of data and materials statement
The datasets supporting the conclusions of this article are included within the article.
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http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
HZW and RW conceived of the study, and participated in data collection, analysis, and interpretation of the results and writing of the manuscript. DYD and YTL contributed to data collection, and interpretation of the results and writing of the manuscript. FLL contributed to the interpretation of the results and writing of the manuscript. All authors read and approved the final manuscript and consented to publish this manuscript.