We investigated the association between plasma ADPN level with some inflammatory and metabolic determinants in CKD patients. Several studies have shown that plasma ADPN level is inversely correlated with some metabolic syndrome factors such as BMI and type 2 diabetic mellitus in the general population (
10). Other studies showed that plasma ADPN level is higher in CKD patients compared with healthy persons (
11). The major mechanisms, can decrease the renal ADPN clearance (
12), dysregulation in the ligand/receptor activity (
13), or a response to metabolic disorders in renal dysfunction (
14). Moreover, higher plasma ADPN level may be the predictor of disease progression in CKD patients (
15).
Our study found that plasma ADPN level inversely correlates with GFR, some metabolic and inflammatory factors such as BMI, CRP, FBS, and HDL-cholesterol levels in CKD patients not in dialysis patients, but it was not associated with other important metabolic syndrome determinants such as total cholesterol, triglyceride, LDL-cholesterol, and other inflammatory markers such as ESR, albumin, and hemoglobin levels in these patients.
Adiponectin, an adipokine secreted by adipocyte, has many systemic effects and important roles in vascular protection. Hypoadiponectinemia is a risk factor for ischemic heart disease, hypertension and endothelial dysfunction in some studies (
16). However, other studies had not found any association between low plasma ADPN level and cardiovascular mortality in the general population (
17).
The role of ADPN in CKD patients is unclear. High plasma ADPN level was significantly correlated with a low risk of cardiovascular events in some studies (
1,
11). Moreover, plasma ADPN level was inversely correlated with other metabolic syndrome determinants such as BMI, FBS, and Triglyceride. It also directly correlated with HDL in CKD patients did not undergo dialysis (
5).
Anti-inflammatory effects of ADPN in CKD patients may be due to inhibition of oxidative stress or induction of macrophage tolerance stimulated by new inflammatory stimuli (
18). Our study had some limitation. First, we measured the total plasma ADPN level while, APDN has at the least three different oligomeric complexes with multiple functions (
19). However, analysis of total ADPN or a specific oligomeric complex in plasma has provided similar results (
20). Second, we analyzed a small number of patients in a single center, so other multicenter studies with large number of patients are required to evaluate the role of ADPN in CKD patients, precisely.
In summary, the results of this study showed that the plasma ADPN was inversely correlated with some determinants of the metabolic syndrome. In addition, plasma total ADPN level was inversely associated with GFR in these patients. Thus, it is concluded that ADPN can be known as an important marker for CKD patients.