ABSTRACT
Aim:
Coronary heart disease is one of the most common causes of death around the world. The pathological process of coronary heart disease like atherosclerosis starts in childhood. During this period thrombosis constitutes a high-risk factor. In this study, we investigated the effect of soluble CD40 ligand (sCD40L) and clotting activation on children and adolescents with hypercholesterolemia.
Materials and Methods:
Plasma levels of sCD40L, P-selectin, 8-hydroxy-2-deoxyguanosine (8-OHdG), and prothrombin fragment 1+2 [(F) 1+2] were determined in thirty-five hypercholesterolemic patients (20 girls and 15 boys; age, median: 13 years) and forty healthy normocholesterolemic subjects (28 girls and 12 boys; age, median: 13 years).
Results:
No significant differences were observed between the patient group and controls in terms of age, high-density lipoprotein (HDL) cholesterol, 8-OHdG, F1+2 (p>0.05). However, there were significant differences between the two groups with respect to total cholesterol, low-density lipoprotein (LDL) cholesterol, very LDL cholesterol, triglycerides, sCD40L and P-selectin (p<0.05), which were higher in the patient group than the controls. A positive correlation was observed between sCD40L and P-selectin (p<0.05) in accordance with the Spearman correlation analysis. The correlation coefficients were 0.735 in the patient group and 0.647 in the control group. But there was no significant correlation between sCD40L and total cholesterol, LDL-cholesterol, HDL-cholesterol, very LDL-cholesterol, triglycerides, 8-OHdG, F1+2 (p>0.05).
Conclusion:
We believe that future prospective studies to determine the increase in the level of sCD40L with a larger sample size of a pediatric population with dyslipidemias may be more helpful in predicting the risk of cardiovascular disease.
Introduction
Coronary heart disease (CHD) and atherosclerosis are the common causes of death around the world. The pathological process of CHD starts in childhood and its clinical effects are generally seen in adult patients. There are a lot of risk factors as underlying mechanisms of atherosclerosis, and one of these factors is hypercholesterolemia. Epidemiologic and clinical trials have provided clear evidence that cholesterol has a role in the occurrence of cardiovascular disorders (1,2). This may be related to enhanced thrombotic risk. Activated platelets adhere to the intact endothelium and induce inflammatory responses locally, which substantially contribute to the early phase of atherosclerosis. It has been seen that patients with hypercholesterolemia have increased urinary excretion of 11-dehydro-thromboxane B2 and elevated platelet response (3). Another study (4) states that the tendency to prothrombotic state is higher when the formation of monocyte tissue factor (TF) is increased, and prothrombin fragment [(F) 1+2] (a marker of thrombin generation in vivo) levels are elevated.
The expression of CD40 ligand (CD40L) is observed on CD4+ T cells, activated platelets, and vascular system cells (endothelial cells (ECs), smooth muscle cells (SMCs) and macrophages) (5,6). The interaction between the CD40L that is expressed on vascular cells, and soluble CD40L (sCD40L) causes inflammatory and prothrombotic responses, resulting in increased atherosclerotic progression (5,7). When CD40 and sCD40L are adhered, TF in SMCs, ECs, and macrophages are over expressed. Thus TF can provide the convertion of factor X to Xa on SMCs within the atherosclerotic plaque (8-10). Previous studies demonstrated that oxidative stress plays a major role in the monocyte expression of TF by promoting nuclear factor-kappa-B activation (11). The plasma level of P-selectin, an activation marker of platelets, can reflect the earlier defects of platelets.
To explore the effect of clotting factors in pediatric CHD pathogenesis, we investigated the behavior of sCD40L and clotting activation in children and adolescents with hypercholesterolemia.
Materials and Methods
Patients and Controls
Thirty-five hypercholesterolemic patients whose low-density lipoprotein (LDL)-cholesterol levels were >155 mg/dL (4 mmol/L) (20 girls and 15 boys; age, median: 13 years, minimum: 4 years, maximum: 18 years) and who had a history of familial hypercholesterolemia, and forty healthy normocholesterolemic subjects (28 girls and 12 boys; age, median: 13 years, minimum: 4 years, maximum: 18 years) were asked to participate in this study. Physical examination showed that none of the patients had any clinical evidence of peripheral vascular or inflammatory diseases. Potential patients with infection, tumor, diabetes, hypertension, hypothyroidism, hypertriglyceridemia, liver or kidney disease were excluded. Other exclusion criteria were, family history of thrombosis, metabolic syndrome, and medication, which might affect inflammatory and thrombotic markers.
The study was approved by the Gazi University Local Ethics Committee (approval number: 015, 21 January 2008) and all patients and their families provided written informed consent.
Blood Samplings
Peripheral venous blood samples were obtained after a 12-hour fast. The lipid profile (ß-quantification) was analyzed on fresh samples. The subjects whose total cholesterol and LDL-cholesterol were >95th percentile according to age and sex were accepted as hypercholesterolemic. Total cholesterol and high-density lipoprotein (HDL) levels were determined by colorimetric-spectrophotometric autoanalyzer (Aeroset®, Abbott®, Illinois, USA) at 500 nm according to the Trinder reaction. LDL levels were calculated according to the Friedewald formula [Total cholesterol - (HDL + very LDL [VLDL])]. Blood samples were immediately centrifuged at 2000 rpm for 20 min at 4 ˚C and the supernatant was collected and stored at-80 ˚C until measurement. Plasma levels of sCD40L, sP-selectin, 8-hydroxy-2-deoxyguanosine (8-OHdG), F1+2 were determined using commercial ELISA kits according to the manufacturers’ instructions (human sCD40L ELISA, Bender Med, Austria; human sP-selectin ELISA, Bender Med, Austria; 8-hydroxy-2 deoxyguanosine ELISA, Northwest Life Science Specialties, LLC, USA; prothrombin F1+2 ELISA, Dade Behring Inc., USA).
Statistical Analysis
Statistical analysis was performed with SPSS 11.5 software for Windows (SPSS Inc., Chicago, Illinois). All results are expressed as mean, standard deviation, median, minimum and maximum. Kolmogorov-Smirnov test was used to verify that the data were within normal distribution.
Mann-Whitney U test was used for the comparison of the groups. The association of measurements with other biochemical parameters was assessed by the Spearman rank correlation test. A p value of <0.05 was considered statistically significant.
Results
Age and laboratory parameters of the patient and control groups are shown in Table I. No significant differences were observed between the patient group and controls in terms of age, HDL-cholesterol, 8-OHdG, F1+2 (p>0.05). On the other hand, there were significant differences with respect to total cholesterol, LDL cholesterol, VLDL cholesterol, triglycerides, sCD40L and P-selectin (p<0.05). These values were higher in the patients than the controls. Serum levels of cholesterol and LDL-cholesterol were 308.7±142.4, 243.7±146.7 mg/dL in subjects with hypercholesterolemia, and 154.2±17.3 and 86.8±17.5 in those with normocholesterolemia. These differences between the two groups were significant (p<0.001). Compared to subjects with hypercholesterolemia, those with normocholesterolemia had higher values of sCD40L, as 3.3±2.8 and 1.9±2.3, respectively (p=0.004). In respect of P-selectin, the levels were 235.6±73.5 in hypercholesterolemic subjects and 209.3±96.1 in normocholesterolemic subjects (p=0.0049).
A positive correlation was observed between sCD40L and P-selectin (p<0.05) (Spearman correlation analysis) (Figure 1). Correlation coefficients were 0.735 in the patient group, and 0.647 in the control group. But there was no significant correlation between sCD40L and total cholesterol, LDL-cholesterol, HDL-cholesterol, VLDL-cholesterol, triglycerides, 8-OHdG, F1+2 (p>0.05) (Table II).
Discussion
This study provides evidence that, increased sCD40L and P-selectin levels, which are known as inflammatory molecules, are involved in the onset and progression of atherosclerotic disease in children with hypercholesterolemia.
Hypercholesterolemia, a risk factor for cardiovascular disease, is associated with inflammation and hypercoagulability. Thrombophilia is a frequent occurrence in patients with hypercholesterolemia, and can precipitate cardiovascular events in this setting.
Thrombophilia is basically characterized by platelet hyperactivation and up-regulation of TF with enhanced thrombin generation (3,4). CD40L may represent an important link between platelet activation and TF expression (5). It has been reported in a study (12) that, considerable increase in sCD40L would help the prediction of probable cardiovascular events problems in healty women. Another study (13) shows that, higher sCD40L would result in recurrent cardiovascular morbidity and mortality because of acute coronary syndromes. In patients with hypercholesterolemia, CD40L is up-regulated on the platelet surface and (14) may therefore represent an important stimulus for TF expression and clotting activation. It has been shown that, there is a significant correlation between sCD40L and prothrombin F1+2 (15). Because CD40L exerts a prothrombotic effect through overexpression of TF, it would be reasonable to speculate that in hypercholesterolemia, clotting activation occurs as a consequence of CD40L overexpression.
This current study aimed to measure the plasma levels of sCD40L and other parameters in children with hypercholesterolemia. Although there are numerous similar studies of adults with hypercholesterolemia, measuring sCD40L concentrations in children with hypercholesterolemia is quite novel. According to our results, sCD40L was significantly higher in hypercholesterolemic patients than the normocholesterolemic control group in childhood. Of course it is important to follow this parameter and the clinical condition of all the subjects in the future for the possibility of coronary syndrome. So we can speculate that this sCD40L parameter can be an indicator to screen the CHD in childhood.
P-selectin is an adhesion molecule known to be involved in the pathogenesis of athero-thrombosis. Being the primary adhesion molecule in initiating cell activation and cell adhesion to platelets, leucocytes and ECs, it’s believed that P-selectin may contribute to endothelial dysfunction, atherosclerosis and thrombosis (16). One research showed that, increased levels of soluble P-selectin with higher levels of cholesterol in obese children, might indicate EC damage and platelet activation (17). In our study, P-selectin level was higher in the hypercholesterolemic patients. Additionally a positive correlation between sCD40L and P-selectin was found. As well as being mediators of inflammation and having a significant effect on atherosclerosis, high levels of P-selectin can be a risk factor for CHD. 8-OHdG is a product of oxidative deoxyribonucleic acid (DNA) damage following specific enzymatic cleavage after 8-hydroxylation of the guanosine base. In recent years, 8-OHdG has been used widely in many studies not only as a biomarker for the measurement of endogenous oxidative DNA damage but also as a risk factor for many diseases including cancer and some degenerative diseases (18). According to our findings, there was no significant difference in the 8-OHdG levels of the hypercholesterolemic children compared to the control group. In a previous study, it was shown that the level of 8-OHdG was lower in hypercholesterolemic and normocholesterolemic children than in adults correspondingly (19). This result can be explained by the fact that age is associated with changes of mechanisms controlling oxidative stress and platelet activation. Therefore, our result can be related to the age of the participants. However, in that study (19) there was a significant correlation between the sCD40 and 8-OHdG levels in both hypercholesterolemic children and the adult group. In our study, we couldn’t find a positive correlation between those parameters. We may explain this result with the limited number of patients in the study population.
F1+2, which comes from in vivo cleavage of prothrombin by factor Xa, is considered to be useful for the diagnosis of thrombosis (20). Increased F1+2 levels have been reported in venous thromboembolism, inflammation, cancer, sepsis, acute coronary syndromes, stroke, peripheral arterial disease, atrial fibrillation, and during the postoperative period. In our study, no relation was found in the F1+2 levels between the patient and the control groups. This result may relate to the differences of the coagulation characteristics in the pediatric population, as variability of these parameters in pediatric population are yet unknown.
In this study, we measured the levels of sCD40L in hypercholesterolemic patients as higher than the healthy control group, which is in accordance with the previous studies (13-15,21). P-selectin levels were higher in the hypercholesterolemic patients than the controls. The expression of CD40 is observed on various cell types such as: ECs, SMCs, macrophages and activated T lymphocytes. The engagement of CD40 and sCD40L triggers atherosclerosis. The expression of vascular cell adhesion molecule-1, intercellular adhesion molecule-1, and P-selectin on ECs facilitate the participation of monocytes and lymphocytes in the injury. Like sCD40L, interleukin (IL)-1, IL-6, and tumor necrosis factor-alpha may have a role in this process. The production of reactive oxygen species are elevated with regard to the CD40-sCD40L engagement, which induces the inhibition of endothelial nitric oxide, causing endothelial dysfunction and promoting atherogenesis (22,23). It is a well-known fact that the degree of the plasma level of cholesterol is directly related to the damage of vascular ECs. This study showed an elevated level of sCD40L in the hypercholesterolemic patients compared to the healthy controls. It was also shown that there was a positive correlation between the level of sCD40L and the level of P-selectin. Therefore, we can speculate that if one of these parameters is normal in range, the other facilitator factor might be decreased. Another important aspect of this study is that the participitants were selected from childhood and the adolescent period. To our knowledge, there are very few studies in the literature that lead to the understanding of the mechanism of premature atherogenesis among children.
Study Limitations
The sample size for the patient group was small.
Conclusion
In conclusion, future prospective studies with a larger sample size might better detect the increased sCD40L level in the setting of a pediatric population with familial dyslipidemias, which may be more helpful in predicting the risk of cardiovascular events.
