Urinary calprotectin, NGAL, and KIM-1 in the differentiation of primarily inflammatory vs. non-inflammatory stable chronic kidney diseases

Ren Fail. 2021 Dec;43(1):417-424. doi: 10.1080/0886022X.2021.1885442.

Abstract

Introduction: It has been demonstrated that urinary neutrophil gelatinase-associated lipocalin (NGAL) and calprotectin are helpful biomarkers in the differentiation of intrinsic and prerenal acute kidney injury.

Objective: The present cross-sectional study investigates, whether urinary biomarkers are able to differentiate primarily inflammatory from non-inflammatory entities in chronic kidney disease (CKD).

Methods: Urinary calprotectin, NGAL, and kidney injury molecule-1 (KIM-1) concentrations were assessed in a study population of 143 patients with stable CKD and 29 healthy controls. Stable renal function was defined as an eGFR fluctuation ≤5 ml/min/1.73 m2 in the past 12 months. Pyuria, metastatic carcinoma, and renal transplantation were regarded as exclusion criteria. Diabetic nephropathy, hypertensive nephropathy, and polycystic kidney disease were categorized as 'primarily non-inflammatory renal diseases' (NIRD), whereas glomerulonephritis and vasculitis were regarded as 'primarily inflammatory renal diseases' (IRD).

Results: Urinary calprotectin and NGAL concentrations significantly differed between CKD and healthy controls (p < 0.05 each), whereas KIM-1 concentrations did not (p = 0.84). The three biomarkers did neither show significant differences in-between the individual entities, nor the two categories of IRD vs. NIRD (calprotectin 155.7 vs. 96.99 ng/ml; NGAL 14 896 vs. 11 977 pg/ml; KIM-1 1388 vs. 1009 pg/ml; p > 0.05 each). Albumin exceeds the diagnostic power of the investigated biomarkers by far.

Conclusions: The urinary biomarkers calprotectin, NGAL, and KIM-1 have no diagnostic value in the differentiation of primarily inflammatory vs. non-inflammatory etiologies of CKD.

Keywords: Calprotectin; KIM-1; NGAL; chronic kidney disease.

Publication types

  • Multicenter Study

MeSH terms

  • Aged
  • Albuminuria / etiology
  • Biomarkers / urine
  • Case-Control Studies
  • Cross-Sectional Studies
  • Diagnosis, Differential
  • Female
  • Germany
  • Glomerular Filtration Rate
  • Hepatitis A Virus Cellular Receptor 1 / analysis*
  • Humans
  • Inflammation / diagnosis
  • Leukocyte L1 Antigen Complex / urine*
  • Lipocalin-2 / urine*
  • Male
  • Middle Aged
  • Renal Insufficiency, Chronic / pathology
  • Renal Insufficiency, Chronic / urine*

Substances

  • Biomarkers
  • HAVCR1 protein, human
  • Hepatitis A Virus Cellular Receptor 1
  • LCN2 protein, human
  • Leukocyte L1 Antigen Complex
  • Lipocalin-2

Grants and funding

The study was funded by the German Research Foundation (Research Unit FOR1368). The funders had no role in study design, data collection, and analysis, decision to publish, or preparation of the manuscript.