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International Journal of Nephrology
Volume 2016, Article ID 2180765, 7 pages
http://dx.doi.org/10.1155/2016/2180765
Research Article

Serum Endocan Levels Associated with Hypertension and Loss of Renal Function in Pediatric Patients after Two Years from Renal Transplant

1Nephrology Division, School of Medicine, Federal University of São Paulo, São Paulo, SP, Brazil
2Pediatrics Department, School of Medicine, Federal University of São Paulo, São Paulo, SP, Brazil

Received 13 September 2016; Accepted 20 November 2016

Academic Editor: Laszlo Rosivall

Copyright © 2016 Livia Victorino de Souza et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Endocan is an important biomarker of inflammation and endothelial dysfunction that increases in association with several chronic diseases. Few published data have described the role of endocan in pediatric renal transplant (RT) patients. We evaluated the endocan concentrations in 62 children who underwent renal transplantation and assessed their relationships with the patients’ blood pressure and loss of renal function. The endocan levels were significantly elevated in the pediatric RT patients who had hypertension and a loss of renal function. We determined positive correlations between the endocan concentrations and the hemodynamic variables (systolic blood pressure: ; ; pulse pressure: ; ). The endocan levels were inversely correlated with the estimated glomerular filtration rate (; ). An endocan cutoff concentration of 7.0 ng/mL identified pediatric RT patients who had hypertension and a loss of renal function with 100% sensitivity and 75% specificity. In conclusion, the endocan concentrations were significantly elevated in pediatric RT patients who had both hypertension and a loss of renal function. The correlations between the endocan levels and the hemodynamic variables and the markers of renal function strengthen the hypothesis that it is an important marker of cardiorenal risk.

1. Introduction

Renal transplantation is one of the most effective options for the treatment of chronic renal failure in children [1, 2]. Children who receive renal transplants (RTs) have better survival rates than children who undergo dialysis [3]. In addition, these children show improvements in the quality of their lives and their life expectancies [3, 4].

Despite a positive prognosis, concerns continue to exist about the progressive loss of renal function and the development of cardiometabolic diseases among pediatric RT recipients [57]. The findings from several studies have demonstrated that hypertension (HT) is a major cardiovascular comorbidity that can follow renal transplantation in pediatric patients [811], and the prevalence of HT among these patients ranges from 60% to 90% [8]. Some investigators have verified that the development or the persistence of HT during the posttransplant period is an important risk factor that is associated with graft loss and survival [811]. Indeed, a negative association between HT and the glomerular filtration rate (GFR) was determined after renal transplantation in children [9]. While several factors may explain this association, the underlying mechanism remains unclear. It is possible that posttransplant HT together with donor and recipient factors, including the time on dialysis, immunosuppressive therapy, the timing of the transplantation, and the donor’s age, converge to negatively impact upon the GFR.

The findings from recent research indicate that endocan could be an important predictive marker of arterial HT and renal failure [1214]. Endocan is a soluble dermatan sulfate proteoglycan that is expressed by the human endothelial cells that are present in many different vascular beds [15, 16]. Its expression is regulated by inflammatory cytokines that induce the upregulation of endocan messenger ribonucleic acid, and the molecule is subsequently released by the endothelial cells [17]. Several reports indicate that the endocan concentrations negatively impact upon the severity of illnesses and the clinical outcomes [14, 18, 19]. The purpose of this study was to analyze the endocan concentrations in pediatric patients during the 6–24-month period after renal transplantation. We also assessed the relationships between the endocan levels and the patients’ blood pressure and loss of renal function.

2. Methods

This study was conducted at the Renal Transplant Unit of the Nephrology Division from Kidney & Hypertension Hospital (Federal University of São Paulo; UNIFESP-EPM, São Paulo, Brazil) on pediatrics patients, who were recruited between August 2013 and July 2014. The study was carried out on 62 RT children (43 boys and 19 girls). Inclusion criteria were as follows: RT patients of either sex; patients who were between 6 and 24 months after transplant. On the other hand, patients were excluded for the following reasons: presence of systemic infection or acute rejection clinically diagnosed and biopsy proven. None of the children who underwent renal transplant received vitamin D supplementation. All patients provided a blood sample, which was collected in the morning, following an overnight fast. After that, the body weight and height were measured using a standard balance beam scale. The local ethics committee approved the study protocol (Protocol Number: 354.875). All parents and children signed written informed consent/assent forms.

2.1. Measurement of Blood Pressure Levels

Systolic (SBP) and diastolic (DBP) blood pressure were measured with appropriate cuff size by auscultation after the child was seated for 10 min. We defined HT in accordance with the Fourth National Task Force on High Blood Pressure in Children and Adolescents [20]. An HT diagnosis was established when three or more assessments of the SBP and/or the DBP on different days over a 21-day interval were above the 95th percentiles at 6 months after transplant. We calculated the pulse pressure (PP) using the following formula: PP = SBP − DBP.

2.2. Renal Function Assay

The serum creatinine (sCr) levels were measured using an automated picric acid assay and a Hitachi 717 analyzer in accordance with the manufacturers’ instructions. The estimated GFR (eGFR) was determined based on the sCr levels using the Bedside Schwartz equation, as follows: (eGFR = 0.413 × height (cm)/Scr [mg/dL] = mL/min/1.73 m2) [21].

2.3. Endocan Measurement

The serum endocan levels were measured using a magnetic bead-based immunoassay kit (HCVD1MAG-67K–1 Plex; Merck Millipore, Billerica, MA, USA), according to the manufacturer’s protocol. The assay’s concentration range was 0.02–9.6 ng/mL. The intra-assay and interassay coefficients of variation for the endocan assay were <2.43% and <5.57%, respectively. Neither significant cross-reactivity nor interference between human endocan and the breakdown product, which is a p14 peptide fragment, has been reported.

2.4. Statistical Analysis

The categorical variables are presented as the frequencies and the percentage distributions. The continuous variables were assessed for normality before the data were analyzed, and they are summarized as the means, standard deviations, and the 95% confidence intervals (CIs). The analyses were performed by stratifying the pediatric RT patients according to the chronic kidney disease (CKD) cutoff point, namely, an eGFR of <60 mL/min/1.73 m2, and the presence or absence of HT [20, 22]. To examine the effects of HT and CKD on the endocan levels, we performed a two-way analysis of variance (ANOVA) followed by pairwise multiple comparisons using the Bonferroni test that examined the significance of the main effect and/or the interactions between HT and CKD. Correlations between the continuous variables were determined using Pearson’s correlation coefficient. Furthermore, logistic regression analyses were performed. Variables that showed a tendency towards a correlation and had a value of in the univariate model were included in the multivariate analysis. A receiver operating characteristic (ROC) curve was applied to identify the best endocan cutoff point. All of the statistical tests were two-tailed, and the significance level was set at . The statistical analyses were performed using IBM®SPSS® software (Version 22, IBM Corporation, Armonk, NY, USA).

3. Results

Our study cohort comprised 62 pediatric RT patients, and 67% of the patients were boys. The mean age of the recipients at transplantation was 12.8 years (range: 3–17 years), and the mean age of the donors was 12.7 years (range: 2–43 years). Six of the donors were adults and 56 donors were younger than 18 years of age. The causes of renal failure were defined as uropathy in 22.6% and glomerulonephritis in 17.7% of the patients, and the etiologies were undetermined or the renal failure was associated with other causes in 59.7% of the RT patients (Table 1). After renal transplantation, 29 of 62 (46.8%) children had CKD, which was defined as an eGFR < 60 mL/min/1.73 m2. HT was detected in 44 of the children before renal transplantation, and HT persisted in 29 of the children after transplantation. Sixteen children had both HT and CKD after renal transplantation, and 20 children had neither HT nor CKD. Seventeen children (26%) were given steroid-free immunosuppressive therapy and seven children (25%) were given single agent antihypertensive therapy that comprised calcium channel blockers (CCBs). Demographic, anthropometric, and clinical data are presented in Tables 1 and 2.

Table 1: Clinical characteristics of the study population at renal transplant.
Table 2: Characteristics of the study population after transplantation.

The mean endocan concentration was 12.2 ng/mL (range: 4.3–15.4 ng/mL), and there was no significant difference between the genders with respect to the endocan concentration (). There were no correlations between the endocan levels and age (; ) or the body mass index (BMI) (; ). We found positive correlations between the endocan levels and the SBP (; ) and the PP (; ) (Figures 1(a) and 1(b)). These correlations remained significant after adjusting for gender, age, BMI, and the time on chronic dialysis (SBP: ; and PP: and ). The serum endocan levels did not change significantly when immunosuppressive or antihypertensive agents were administered (both ). Inverse correlations were detected between the eGFR and the SBP (; ) and the PP (; ). Interestingly, endocan levels were inversely correlated with the eGFR (; ).

Figure 1: Scatter plots showing the correlations between endocan with (a) systolic blood pressure (; ) and endocan with (b) pulse pressure (; ). The lines represent the weighted regression with its 95% confidence interval. Statistical analysis: Pearson’s correlation method.

The two-way ANOVA revealed the significant effects of HT (; ) and CKD (; ) on the serum endocan concentrations (Figure 2(a)). Pediatric RT patients with HT and CKD () had a significantly higher mean serum endocan concentration (15.4 ng/mL; 95% CI: 13.8–17.2) compared with that in the pediatric RT patients who did not have either of these conditions () (8.9 ng/mL; 95% CI: 7.4–10.5) () and the mean serum endocan concentration in those with HT only () (10.8 ng/mL; 95% CI: 8.9–12.6) (). There was no significant difference with respect to the mean serum endocan concentration between the pediatric RT patients with HT and CKD and those with CKD only () (13.1 ng/mL; 95% CI: 11.2–14.9) () (Figure 2(b)). The mean serum endocan concentration in the pediatric RT patients with only CKD was significantly higher compared with that in the pediatric RT patients who did not have HT or CKD () (Figure 2(b)).

Figure 2: (a) Interaction plot of the mean endocan levels in RT children () according to presence or not of the hypertension (HT) and/or chronic kidney disease (CKD). Statistical analysis: two-way analysis of variance (ANOVA) method. (b) Changes in the endocan levels in RT children with both HT and CKD (HTCKD; ), with HT without CKD (HT w/o CKD; ), with CKD without HT (CKD w/o HT, ), and without both conditions (w/o HTCKD; ). The bars indicate standard error of mean. Statistical analysis: two-way analysis of variance (ANOVA) followed by pairwise multiple comparison (Bonferroni test) method. versus w/o HTCKD; versus HT w/o CKD; versus w/o HTCKD.

We performed logistic regression analyses to identify the risk factors associated with HT and the loss of renal function in the pediatric RT patients. The univariate analysis showed that donor age, a male donor, the PP, and the use of prednisone tended to be associated with these dependent variables () (Table 3). The endocan levels were independently associated with the presence of HT and the loss of renal function in the pediatric RT patients (Table 3). The multivariate logistic regression analysis determined that only the endocan levels were independently associated with the presence of HT and the loss of renal function in our study population (Table 3). The ROC curve analysis demonstrated that an endocan cutoff concentration of 7.0 ng/mL could identify pediatric RT patients with both HT and the loss of renal function with a sensitivity of 100% and a specificity of 75% (area under the curve:  0.894; standard error: 0.053; 95% CI: 0.790–0.998; ) (Figure 3).

Table 3: Logistic regression analysis for the presence of hypertension and chronic kidney disease (CKD) in RT children.
Figure 3: Receiver operating characteristic (ROC) curve of endocan levels predicting presence of both hypertension and loss renal function in RT children.

4. Discussion

The main finding of present study is that serum endocan levels were significantly elevated in RT children with both HT and loss of renal function and that the serum endocan concentration was an independent predictor of the presence of HT and a loss of renal function in pediatric RT patients, after adjusting for multiple confounders. In addition, we found positive correlation of endocan with SBP and pulse pressure, and the serum levels of this biomarker were inversely correlated with eGFR among RT children.

Endocan is a soluble proteoglycan that is detected in the blood and is expressed by endothelial cells of the vasculature, lung, and kidney [16, 17]. There is strong evidence to support its role in several chronic diseases and that suggests that it is an important biomarker of endothelial function [13, 18, 19]. The findings from a recent study showed that patients with type 2 diabetes who had microalbuminuria had lower endocan levels [23], and the investigators suggested that higher levels of endocan may be present in the early phase of diabetic nephropathy and that the levels of endocan decline as the disease progresses [23]. To date, few studies have evaluated the role of the endocan levels in RT patients. The findings from a study by Li et al. [24] showed that the circulating endocan level could be used as a marker of acute rejection in RT patients. In another report, high levels of endocan were correlated with different stages of the CKD in RT patients [25]. These authors also observed that GFR loss was greater in the group with higher serum endocan levels [25]. In addition, negative correlations have been described between the endocan levels and the eGFR and endothelial function in patients with CKD who had not undergone hemodialysis or peritoneal dialysis [13]. Our results concur with and extend the findings from these studies, and they link high endocan levels with HT and GFR reductions in RT patients. Another interesting finding was the positive association between the endocan levels and the PP. Furthermore, we found that pediatric RT patients who had HT and a loss of renal function also had higher PPs compared with the pediatric RT patients who did not have these conditions. The PP elevations observed in these children might indicate the presence of arterial stiffness that leads to adverse cardiovascular outcomes. The impairment of the elastic properties of the vasculature is widely regarded as a factor that could contribute to the development and/or the persistence of HT and CKD progression [26]. Interestingly, endocan is involved in the development of vascular tissue under physiological and pathological conditions [2730]. An important consideration is that treatment with antihypertensive and/or immunosuppressive agents may have an effect on the endocan levels. Some drugs, including angiotensin II receptor blockers, tacrolimus, and CCBs, promote alterations in endothelial function that could also influence the circulating endocan levels [31, 32]. In the current study, there were no significant changes in the serum endocan levels that were associated with the administration of immunosuppressive or antihypertensive therapy. Therefore, therapeutic scheme in the RT patient should be taken into account which makes the interpretation of endocan data among these patients even more difficult.

Some mechanisms could explain the high endocan levels in the pediatric RT patients with HT and the loss of renal function. The findings from recent studies have shown links between the endocan levels and endothelial dysfunction and inflammation [13, 18, 19]. Endocan is expressed by the endothelium, and in response to endothelial damage or the presence of inflammatory cytokines, including tumor necrosis factor-alpha and interleukin-1 beta, the endothelial cells upregulate the expression and secretion of endocan [1517]. Endocan may stimulate the proliferation and migration of vascular smooth muscle cells [33]. Since endothelial dysfunction and inflammatory factors are associated with the development of HT and other cardiovascular diseases in RT patients, it is possible that the presence of these conditions could, at least in part, reflect the processes that were involved in increasing the endocan levels in our study population. Moreover, the increase in the endocan levels in patients with CKD may be a consequence of a reduction in its renal clearance [13]. We did not collect urine samples from the patients in the present study; therefore, we could not compare the fractional excretions of endocan in the pediatric RT patients. However, based on data recently reported in the literature, the high endocan levels in the pediatric RT patients do not appear to have been caused by reductions in the renal clearance of endocan, which results in high concentrations of endocan in the plasma [31]. Endocan is a negatively charged 50 kDa proteoglycan; therefore, under physiological conditions it cannot pass through the glomerular filtration barrier [17, 31]. Indeed, recent study found that endocan was undetectable or was present at very low levels in urine samples from healthy individuals [31]. The same investigators also found that both the plasma and the urinary concentrations of endocan were high in patients with immunoglobulin A nephropathy, which suggests that the presence of glomerular injury that involves the disruption of the basement membrane in patients with pathological renal conditions could promote endocan excretion into the urine [31]. Thus, more knowledge about renal handling of endocan is required to help us understand the mechanisms involved in the production of endocan and its clearance from the circulation via the kidney in RT patients.

The limitations of the present study include the small number of patients recruited, its cross-sectional design, and the single rather than multiple measurements of the serum endocan concentrations. In conclusion, pediatric RT patients with both HT and a loss of renal function have elevated endocan levels. The presence of correlations between the endocan levels and the SBP, the PP, and the eGFR strengthens the hypothesis that endocan is an important marker of cardiorenal risk. Although the pathological implications are not completely understood, the data from this study may help to explain the kidney damage and the increased risks of HT and other cardiovascular diseases that occur in pediatric RT patients. Further studies are necessary to clarify the importance of these correlations and to elucidate the clinical significance of endocan.

Competing Interests

The authors declare that they have no competing interests.

Acknowledgments

This research was supported by a Project Grant from the FAPESP (Fundação de Amparo à Pesquisa do Estado de São Paulo, Brazil) (Project no. 2013/03139-0) and CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico) (Project no. 443248/2014-1).

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