Update of pathophysiology and management of diabetic kidney disease

J Formos Med Assoc. 2018 Aug;117(8):662-675. doi: 10.1016/j.jfma.2018.02.007. Epub 2018 Mar 2.

Abstract

Diabetic kidney disease (DKD) is a major cause of morbidity and mortality in patients with diabetes mellitus and the leading cause of end-stage renal disease in the world. The most characteristic marker of DKD is albuminuria, which is associated with renal disease progression and cardiovascular events. Renal hemodynamics changes, oxidative stress, inflammation, hypoxia and overactive renin-angiotensin-aldosterone system (RAAS) are involved in the pathogenesis of DKD, and renal fibrosis plays the key role. Intensified multifactorial interventions, including RAAS blockades, blood pressure and glucose control, and quitting smoking, help to prevent DKD development and progression. In recent years, novel agents are applied for preventing DKD development and progression, including new types of glucose-lowering agents, pentoxifylline, vitamin D analog paricalcitol, pyridoxamine, ruboxistaurin, soludexide, Janus kinase inhibitors and nonsteroidal minerocorticoid receptor antagonists. In this review, recent large studies about DKD are also summarized.

Keywords: Albuminuria; Diabetes mellitus; Diabetic kidney disease (DKD); Diabetic nephropathy (DN).

Publication types

  • Review

MeSH terms

  • Albuminuria / complications
  • Albuminuria / diagnosis*
  • Biomarkers
  • Diabetic Nephropathies / physiopathology*
  • Diabetic Nephropathies / prevention & control*
  • Diabetic Nephropathies / therapy*
  • Disease Progression
  • Humans
  • Kidney Failure, Chronic / complications
  • Pentoxifylline / pharmacology
  • Renin-Angiotensin System / drug effects

Substances

  • Biomarkers
  • Pentoxifylline