Inflammatory parameters are independently associated with urinary albumin in type 2 diabetes mellitus

JF Navarro, C Mora, M Macıéa, J Garcıéa - American Journal of Kidney …, 2003 - Elsevier
JF Navarro, C Mora, M Macıéa, J Garcıéa
American Journal of Kidney Diseases, 2003Elsevier
BACKGROUND:: Data about the relationship of inflammation to nephropathy in type 2
diabetes mellitus are scarce. In the present study, we test the hypothesis that inflammatory
parameters are independently related to urinary albumin excretion (UAE) at early stages of
nephropathy. METHODS:: Sixty-five patients with type 2 diabetes with microalbuminuria
(MAB) or mild proteinuria (protein< 1 g/d) were included. We analyzed serum concentrations
of high-sensitivity C-reactive protein (hs-CRP) and tumor necrosis factor-α (TNF-α), as well …
BACKGROUND
Data about the relationship of inflammation to nephropathy in type 2 diabetes mellitus are scarce. In the present study, we test the hypothesis that inflammatory parameters are independently related to urinary albumin excretion (UAE) at early stages of nephropathy.
METHODS
Sixty-five patients with type 2 diabetes with microalbuminuria (MAB) or mild proteinuria (protein < 1 g/d) were included. We analyzed serum concentrations of high-sensitivity C-reactive protein (hs-CRP) and tumor necrosis factor-α (TNF-α), as well as urinary level of this cytokine.
RESULTS
Inflammatory parameters were significantly greater in patients with diabetes than controls; furthermore, urinary TNF-α levels increased significantly as nephropathy progressed. Median urinary TNF-α level was 7 pg/mg in normoalbuminurics, 13 pg/mg in microalbuminurics (P < 0.001), and 18 pg/mg in proteinurics (P < 0.001 versus normoalbuminuria and P < 0.01 versus MAB). Albuminuria was related to hs-CRP (r= 0.68; P < 0.001) and serum (r = 0.45; P < 0.01) and urinary TNF-α levels (r = 0.71; P < 0.001), but there was no association between serum and urinary TNF-α levels. Partial correlation analysis showed that hs-CRP level, urinary TNF-α level, duration of diabetes, and glycated hemoglobin level remained significantly associated with UAE. A stepwise multiple regression analysis showed that UAE was significantly associated with hs-CRP level (P < 0.001), duration of diabetes (P < 0.001), urinary TNF-α level (P < 0.01), and glycated hemoglobin level (P < 0.05; adjusted R2 = 0.73; P < 0.001).
CONCLUSION
Inflammatory parameters in patients with type 2 diabetes at an early stage of nephropathy are independently associated with UAE. In addition to traditional metabolic and hemodynamic factors, it is possible to hypothesize on the participation of inflammation in the pathogenesis of diabetic nephropathy.
Elsevier