Association of Peripheral Nesfatin-1 With Early Stage Diabetic Nephropathy Publisher



Irannejad A¹ ; Ghajar A¹ ; Afarideh M¹ ; Khajeh E¹ ; Noshad S¹ ; Esteghamati S¹ ; Afshari K¹ ; Kahe F¹ ; Ganji M¹ ; Saadat M¹ ; Nakhjavani M¹ ; Esteghamati A¹
Source: Pathophysiology Published:2017

Abstract

Background Nesfatin-1 is a newly found anorectic neuropeptide with potent metabolic regulatory effects that its circulating levels are shown to be elevated in diabetes. We compared serum nesfatin-1 in patients with type 2 diabetes and microalbuminuria (30 mg/day ≤ urinary albumin excretion (UAE) <300 mg/day) with their control patients with type 2 diabetes and normoalbuminuria (UAE <30 mg/day). Patients and methods In a cross sectional setting, 44 adult patients with type 2 diabetes and microalbuminuria and 44 control patients with type 2 diabetes and normoalbuminuria were evaluated. Serum levels of nesfatin-1 along with demographic, clinical and biochemical factors associated with diabetes was measured. Results Mean peripheral concentrations of nesfatin-1 were significantly higher in patients with diabetes who had microalbuminuria compared to normoalbuminuric control patients (175.27 ± 25.96 pg/ml vs. 134.66 ± 23.18 pg/ml, respectively; p value < 0.001). Significant positive correlations were found between circulating nesfatin-1 levels and the following case-mix variables: duration of diabetes, glycated hemoglobin, plasma creatinine, UAE and serum uric acid. In the multivariate logistic regression and after adjustment for a constellation of potentially confounding variables associated with diabetic kidney disease (DKD), circulating nesfatin-1 was the only variable significantly associated with microalbuminuria (odds ratio [95% confidence interval] = 1.224 [1.007–1.487], p value = 0.042). Conclusion In patients with type 2 diabetes, circulating nesfatin-1 appears to be associated with microalbuminuria independent of other established risk factors of DKD. The underlying pathophysiological mechanisms and the prognostic significance of this association remain to be elucidated. © 2016 Elsevier B.V.