Insights into predicting diabetic nephropathy using urinary biomarkers

Biochim Biophys Acta Proteins Proteom. 2020 Oct;1868(10):140475. doi: 10.1016/j.bbapap.2020.140475. Epub 2020 Jun 20.

Abstract

Diabetic nephropathy (DN) is a serious complication of diabetes caused by changes in the structure and function of the kidneys. It is important to detect diagnostic biomarkers of DN at an early stage, in which the drug can slow the loss of kidney function and prevent disease progression. In recent years, a variety of biological markers related to DN have been discovered, which is of great significance for predicting the occurrence and development of diseases. Due to the simplicity of non-invasive collection, urine is an ideal biological sample for the discovery of new biomarkers of kidney disease. We reviewed some new urinary biomarkers related to early DN patients, including urinary proteins, peptides, and exosomes biomarkers. We also highlight the proteins associated with tubular damage, glomerular damage, inflammation and oxidative stress marker. Despite the promise of these new urinary biomarkers, we next proposed a review of the most recent publications reporting on larger cohorts, focusing on those that aim at qualification or validation. This review provides important data to better understand biomarkers related to the pathophysiology of DN, and these markers have been increasingly studied for disease progression to provide effective human treatment.

Keywords: Biomarker; Diabetic nephropathy; Exosomes; Peptide; Proteomics.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Biomarkers / urine*
  • Computational Biology / methods
  • Diabetic Nephropathies / diagnosis*
  • Diabetic Nephropathies / etiology
  • Diabetic Nephropathies / metabolism
  • Diabetic Nephropathies / urine*
  • Early Diagnosis
  • Exosomes / metabolism
  • High-Throughput Screening Assays
  • Humans
  • Inflammation Mediators / urine
  • Oxidative Stress
  • Peptides / urine
  • Prognosis
  • Proteomics / methods

Substances

  • Biomarkers
  • Inflammation Mediators
  • Peptides