Cardiotrophin-1 is not associated with carotid or coronary disease and is inversely associated with obesity in patients undergoing coronary angiography

Abstract

Introduction

Cardiotrophin-1 (CT-1) is a member of the interleukin-6 superfamily with known hypertrophic and protective actions upon cardiac myocytes. Although its effects on myocardial tissue and its role in hypertensive heart disease are well documented, there are no studies on CT-1 blood levels in patients with coronary artery disease. In this study we aimed to verify the relationships of serum CT-1 with vascular disease and metabolic parameters in a population of patients undergoing coronary angiography due to clinical indications.

Material and methods

Serum levels of CT-1 were investigated in a cohort of 81 consecutive patients (median age 68 years (95% CI: 64–71), 59 males) undergoing coronary angiography and carotid Doppler ultrasound. Exclusion criteria were: acute coronary syndrome, already-established ischemic cardiopathy, chronic inflammatory diseases and presence or past history of cancer.

Results

Levels of CT-1 were inversely correlated with body mass index (BMI) and waist circumference (WC) (ρ = –0.261, p = 0.02; ρ = –0.224, p = 0.05, respectively). Moreover, obese patients showed significantly lower CT-1 concentrations than non-obese ones (1.18 (0.64–1.64) ng/ml vs. 1.56 (1.37–2.04) ng/ml, p = 0.013), and serum CT-1 was significantly reduced in patients with elevated compared to those with normal WC (1.43 (0.94–1.60) ng/ml vs. 1.64 (1.39–2.49) ng/ml, p = 0.047). Concentrations of CT-1 did not correlate either with the other parameters of metabolic syndrome or with markers of cardiovascular disease (carotid intima-media thickness, presence of carotid or coronary artery plaques).

Conclusions

Our results failed to demonstrate any association between CT-1 and carotid or coronary disease. The inverse association with BMI and WC fits with the latest experimental data on the role of CT-1 in dysmetabolic conditions and could help to further clarify the role of CT-1 in obesity and diabetes.

Introduction

Cardiotrophin-1 (CT-1) is a member of the interleukin-6 (IL-6) superfamily, which shares the transmembrane signaling protein glycoprotein (gp) 130 as a receptor. It was originally identified as a factor that could induce hypertrophy on cardiac myocytes in vitro [1], but it has been shown to be widely expressed in various adult human tissues including muscle, heart, liver and adipose tissue [2]. To date, CT-1 has been mainly studied for its effects on myocardial tissue and its role in hypertensive heart disease is well documented [3]. Designed primarily to function as a cardiomyocyte survival factor, chronic and excessive activation of CT-1 signaling has been postulated to be harmful, contributing to pathologic left ventricular hypertrophy and myocardial fibrosis [4].

Recently, growing interest has been focused on CT-1's role in adipocyte metabolism and atherogenic conditions, since other gp-130 receptor ligands, such as ciliary neurotrophic factor (CNTF) and interleukin-6 (IL-6), have been shown to affect body weight regulation and glucose tolerance [5–9]. The recent milestone study by Moreno-Aliaga et al. showed that mice lacking CT-1 develop a sort of metabolic syndrome (MS), characterized by adult-onset obesity, hyperglycemia, hyperinsulinemia and dyslipidemia, mainly due to insulin resistance and impaired fat mobilization, and evidenced the anti-obesity properties of chronic recombinant CT-1 (rCT-1) administration not only in CT-1^–/– mice, but also in other models of obese mice, proposing a possible therapeutic use of rCT-1 in obesity and type 2 diabetes [10]. However, an apparent contradiction is raised by the attempt to fit these experimental results with previous studies on CT-1 levels in humans, which, conversely, reported that MS, obesity and hypertension are associated with elevated CT-1 concentrations [11–13].

In contrast with the amount of experimental and clinical literature on CT-1 in hypertensive heart disease, there are no studies on CT-1 blood levels in patients with coronary artery disease. Therefore, based on its effects on both cardiac muscle and metabolism, in the present study we aimed to verify the relationships of serum CT-1 with vascular disease and metabolic parameters in a population of patients undergoing coronary angiography due to clinical indications.

Material and methods

Serum levels of CT-1 were investigated in a cohort of 81 consecutive patients undergoing coronary angiography due to clinical indications in our Cardiology Unit between October 2010 and April 2011. All patients met the AHA/ACC class I indication for coronarography [14]: 30 subjects (37%) had high risk criteria on non-invasive cardiovascular tests, in absence of symptoms, 21 (26%) had stable symptoms of ischemic heart disease and high risk criteria on non-invasive cardiovascular tests, and 30 (37%) had symptoms of incipient congestive heart failure (CHF) with angina and/or non-invasive tests suggestive of reversible myocardial ischemia. Patients with acute coronary syndrome, already-established ischemic cardiopathy (documented by previous coronarography or with regional wall motion abnormalities), chronic inflammatory diseases and presence or past history of cancer were excluded.

Anthropometric and biochemical parameters were measured, and each patient underwent carotid Doppler ultrasound for evaluation of carotid artery intima-media thickness (cIMT) and detection of atherosclerotic plaques. All blood samples were drawn after 8 h of fasting. Body mass index (BMI) was calculated using the following formula: weight (kg)/height² (m). Carotid artery intima-media thickness was computed as the maximum value from determinations in three tracts (common carotid, at one centimeter from the bifurcation and in the internal carotid artery), and carotid atherosclerotic plaque was defined as a focal thickening greater than 2 mm. Coronary artery disease was defined as the presence of at least 50% stenosis in at least one major coronary artery. Serum CT-1 was determined using a home-made ELISA technique, essentially not different from that described by Moreno-Aliaga et al. [10]. Briefly, a 96-well plate was coated with monoclonal antibody MAB438 (R&D, Illinois, USA) at 0.2 µg/well in 100 µl of phosphate buffer saline (PBS at pH 7.4) for 18 h at 4°C. After washing, the plate was blocked for 2 h at 37°C with PBS containing 0.1% casein and rinsed twice with PBS containing 0.05% tween-20 (PBST). Serum samples mixed in sample diluent (0.5% tween-80 and 1% BSA) were then added. After overnight incubation at 4°C, plates were rinsed three times with PBST and incubated with a biotin-labeled rabbit secondary polyclonal antibody against human CT-1 (generated in our laboratory by injecting rabbits with recombinant CT-1) diluted 1: 2000 in PBST for 2 h at 37°C. The plate was then rinsed three times with PBST and incubated for 30 min at room temperature with 100 µl/well of 1: 5000 diluted streptavidin-peroxidase complex (PIERCE, Illinois, USA). Finally, plates were washed five times with PBST and developed with TMB substrate. After stopping the reaction with sulfuric acid, absorbance was measured at 450 nm.

Statistical analysis

Data are expressed as median (95%CI) or number and frequency (%), as appropriate. Mann-Whitney U-test was used to compare independent variables between two groups and correlations were carried out by Spearman's rank correlation. Statistical significance was assumed at p < 0.05. Statistical analyses were performed by using SPSS software (version 17.00; SPSS Inc., Chicago, IL, USA).

Results

The main features of the study group are listed in Table I. Median age was over 65 years old, with a clear prevalence of males (73%). Median BMI was in the range of overweight, and there were high prevalences of diabetes, hypertension, dyslipidemia and MS, as expectable in a population of candidates for coronary angiography. Vascular complications, i.e. myointimal carotid thickening, carotid plaques and coronary disease, were evidenced in percentages fluctuating around 50%.

Table I.

Epidemiologic, anthropometric and metabolic features of the study group

Variable	Results
Age [years]	68 (64–71)
Sex (M/F)	59/22
Body mass index [kg/m2]	27.4 (26.7, 28.4)
Waist circumference [cm]	101 (98–103)
Glucose [mg/dl]	97 (94–103)
Diabetes	25 (30.9%)
Hypertension	66 (81.5%)
Hypo-HDL (< 40 mg/dl in men or < 50 mg/dl in women)	41 (50.6%)
Hypertriglyceridemia (> 150 mg/dl or treated)	25 (30.9%)
Metabolic syndrome	36 (44.4%)
Cardiotrophin-1 [ng/ml]	1.5 (1.35–1.65)
Intima-media thickness, > 1.1 mm	34 (42%)
Carotid artery disease, presence of plaques	48 (59.3%)
Coronary artery disease, mono or multivessel	39 (48.1%)

Data reported as median (95% CI) or number and frequency (%)

While not significantly different between patients with and without MS (Table II), CT-1 levels were inversely correlated with body mass index (BMI) (ρ = –0.26, p = 0.02), and obese patients (BMI ≥ 30 kg/m²) showed significantly lower CT-1 concentrations than non-obese ones (Table II and Figure 1). Accordingly, CT-1 levels were inversely correlated with waist circumference (WC) (ρ = –0.224, p = 0.046), and serum CT-1 was significantly reduced in patients with elevated WC (> 102 cm in men and > 88 cm in women) compared to those with normal WC according to the criteria of the National Cholesterol Education Program Adult Treatment Panel III guidelines [15] (Table II and Figure 1). However, CT-1 concentrations were not associated with the other parameters of MS (diabetes, hypertension, HDL cholesterol, triglycerides), nor with vascular disease (cIMT, presence of carotid or coronary artery plaques) (Table II). Furthermore, CT-1 levels were unrelated to clinical symptoms at presentation (no symptoms, stable angina or symptoms of incipient CHF) and no differences were observed between subjects with different indications for coronary angiography (data not shown).

Table II.

CT-1 serum concentrations according to the metabolic or vascular diagnosis of interest

Variable	CT-1 concentrations [ng/ml]		Value of p
	Yes	No
Obesity (BMI ≥ 30 kg/m2)	1.18 (0.64–1.64)	1.56 (1.37–2.04)	0.013
Elevated WC (> 102 cm in men and > 88 cm in women)	1.43 (0.94–1.60)	1.64 (1.39–2.49)	0.047
Diabetes	1.45 (1.25–1.77)	1.60 (1.30–2.02)	0.870
Hypertension	1.64 (1.35–3.41)	1.49 (1.23–1.72)	0.187
Hypo-HDL (< 40 mg/dl in men or < 50 mg/dl in women)	1.41 (0.98–1.54)	1.65 (1.37–2.34)	0.069
Hypertriglyceridemia (> 150 mg/dl or treated)	1.48 (1.33–1.65)	1.60 (1.23–2.40)	0.516
Metabolic syndrome	1.55 (1.21–2.01)	1.47 (1.35–1.92)	0.78
Intima-media thickness, > 1.1 mm	1.56 (1.33–2.50)	1.45 (1.15–1.77)	0.270
Carotid artery disease, presence of plaques	1.48 (1.02–2.40)	1.51 (1.35–1.72)	0.996
Coronary artery disease, mono or multivessel	1.55 (1.33–1.92)	1.46 (1.23–2.02)	0.737

Figure 1.

Reduced CT-1 level in patients with obesity (A) and increased waist circumference (B). Data are reported as median, error bars represent 95% CI

Discussion

The present results, obtained in a population of candidates for coronary angiography, fail to demonstrate any association between CT-1 serum levels and carotid or coronary disease, while they are the first to find an inverse association between CT-1 circulating concentrations, and whole body and abdominal obesity in humans.

Cardiotrophin-1 is a member of the gp130 family of cytokines which has been widely studied for its effects on myocardial cells and its possible role in cardiac pathophysiology [2, 12]. Cardiotrophin-1 is produced by cardiomyocytes and non-cardiomyocytes in situations of biomechanical stress and activates different signaling pathways leading to cardiomyocyte hypertrophy as well as to myocardial fibrosis [3]. Actually, elevated blood CT-1 concentrations have been found in hypertensive patients [12, 16], higher in those with left ventricular hypertrophy and dysfunction [16, 17], and progressively increasing along with progression of heart failure stages [16].

Recent evidence has demonstrated that gp130 receptor ligands, such as CNTF and IL-6, can affect the balance between calorie procurement and disposal [5–9]. Ciliary neurotrophic factor can induce weight loss by effects on hypothalamic control of energy balance [18], and it has been proposed as a potential treatment for obesity and diabetes [19]. The effects of IL-6 on energy metabolism remain controversial, and the discovery that IL-6 is produced and released from skeletal muscle during exercise [20] has challenged the classical view that it is a proinflammatory cytokine inducing insulin resistance and diabetes [8]. Most of CT-1's metabolic properties have been recently described by the study of Moreno-Aliaga et al., who demonstrated that CT-1^–/– mice develop mature-onset obesity, insulin resistance, and hypercholesterolemia despite reduced calorie intake, and that treatment with rCT-1 reduces adiposity and corrects insulin resistance in genetic and acquired models of obesity in mice [10]. Actually, these data seemed to challenge previous studies in humans, which reported elevated CT-1 levels in patients with hypertension and MS [11–13].

In this context, our study was the first to analyze serum CT-1 concentrations in patients undergoing coronary angiography. Consistent with the experimental background, but in discordance with studies in dysmetabolic patients [11–13], our results did not show associations between CT-1 and any component of the MS, while demonstrating an even inverse association of CT-1 with BMI and WC. We think that this apparent contradiction can be partially solved by analyzing carefully patient characteristics in the different studies. While Natal et al. determined serum CT-1 in “137 apparently healthy subjects free from clinically apparent atherosclerotic disease” [13], Pemberton et al. did so in 59 untreated and treated hypertensive patients without other specified comorbidities or complications [11], and Lopez et al. did so in 111 hypertensive patients without “clinical manifestations of ischaemic heart disease” [12], our study population consisted of patients who, even in the absence of already-established cardiac ischemic disease, did obtain a clinical indication for coronary angiography. Indeed, a significant proportion of our patients showed cardiovascular disease after examination (Table I), suggesting a long history of atherogenic morbidities. Therefore, as already proposed by Moreno-Aliaga et al. [10], it could be speculated that increased serum CT-1 could serve to counteract fat accumulation and metabolic-related complications in early obesity and MS, while this protective mechanism may fail in the late dysmetabolic patient, possibly due to a sort of exhaustion with a further negative impact at least on weight control. After all, insulin history has already indicated similar profiles in the same context: early hyperproduction to counteract hyperglycemia and late exhaustion which leads to type 2 diabetes.

Consistent with the lack of association between CT-1 and cardiovascular risk factors, we did not find any association between serum CT-1 and carotid or coronary artery disease. However, only studies including patients with a wider profile of CV risk could definitely clarify this issue.

In conclusion, our results, obtained in a population of candidates for coronary angiography, do not support any relationship between serum CT-1 and carotid or coronary artery disease, while they could help to solve the apparent contradiction raised by previous clinical and experimental studies on the metabolic roles of CT-1 in humans in vivo.