Association of Complement and Inflammatory Biomarkers with Diabetic Nephropathy

Ann Clin Lab Sci. 2019 Sep;49(4):488-495.

Abstract

Objective: To investigate the association between complement and inflammatory biomarkers with diabetic nephropathy (DN) in type 2 diabetes mellitus (T2DM).

Methods: Plasma and urinary complement and inflammatory biomarkers were measured in 115 T2DM patients assigned to one of two groups: with DN (n=48) and without DN (n=67).

Results: The plasma and urinary levels of C3a, C4d, C5a, sC5b-9 and MBL (mannan-binding lectin) were significantly higher in T2DM patients with DN compared to T2DM patients without DN. The plasma levels of IL-10 and INF-γ, as well as the urinary levels of INF-γ and TNF-α in T2DM patients with DN, were significantly higher than T2DM patients without DN. Both urinary MBL and INF-γ were independent risk factors for DN within T2DM patients (OR, 2.35 (95% CI 2.28-2.64) and 1.17 (95% CI 1.15-1.18); P=0.000 and 0.016, respectively). The area under the receiver-operating-characteristic-curve for urinary MBL was 0.89, with sensitivity 91% and specificity 83% for DN. The area under the receiver-operating-characteristic-curve for INF-γ was 0.84, with sensitivity 86% and specificity 79% based on cutoff values of 1.42 ng/mg and 5.15 pg/mg, respectively.

Conclusion: This study suggests that urinary INF-γ and MBL levels are independent risk factors with a high predictive power for DN in T2DM patients.

Keywords: Complement activation; Diabetic nephropathy; Inflammatory cytokine; Risk factor; Type 2 diabetes mellitus.

MeSH terms

  • Adult
  • Aged
  • Area Under Curve
  • Biomarkers / blood*
  • Biomarkers / urine
  • Complement System Proteins / metabolism*
  • Complement System Proteins / urine
  • Diabetic Nephropathies / blood*
  • Diabetic Nephropathies / urine
  • Female
  • Humans
  • Inflammation / blood*
  • Inflammation / urine
  • Inflammation Mediators / blood
  • Inflammation Mediators / urine
  • Male
  • Middle Aged
  • Multivariate Analysis
  • ROC Curve

Substances

  • Biomarkers
  • Inflammation Mediators
  • Complement System Proteins