Novel Insights in the Physiopathology and Management of Obesity-Related Kidney Disease

Nutrients. 2022 Sep 22;14(19):3937. doi: 10.3390/nu14193937.

Abstract

Obesity is recognized as an independent risk factor for the development of kidney disease, which has led to the designation of obesity-related glomerulopathy (ORG). Common renal features observed in this condition include glomerular hypertrophy, glomerulosclerosis, haemodynamic changes and glomerular filtration barrier defects. Additionally, and although less studied, obesity-related kidney disease also involves alterations in renal tubules, including tubule hypertrophy, lipid deposition and tubulointerstitial fibrosis. Although not completely understood, the harmful effects of obesity on the kidney may be mediated by different mechanisms, with alterations in adipose tissue probably playing an important role. An increase in visceral adipose tissue has classically been associated with the development of kidney damage, however, recent studies point to adipose tissue surrounding the kidney, and specifically to the fat within the renal sinus, as potentially involved in the development of ORG. In addition, new strategies for the treatment of patients with obesity-related kidney disease are focusing on the management of obesity. In this regard, some non-invasive options, such as glucagon-like peptide-1 (GLP-1) receptor agonists or sodium-glucose cotransporter-2 (SGLT2) inhibitors, are being considered for application in the clinic, not only for patients with diabetic kidney disease but as a novel pharmacological strategy for patients with ORG. In addition, bariatric surgery stands as one of the most effective options, not only for weight loss but also for the improvement of kidney outcomes in obese patients with chronic kidney disease.

Keywords: chronic kidney disease; obesity; obesity-related glomerulopathy; renal sinus adipose tissue; visceral adipose tissue.

Publication types

  • Review

MeSH terms

  • Diabetic Nephropathies* / etiology
  • Glucagon-Like Peptide 1 / agonists
  • Humans
  • Hypertrophy / complications
  • Lipids
  • Obesity* / complications
  • Obesity* / therapy
  • Sodium-Glucose Transporter 2

Substances

  • Lipids
  • Sodium-Glucose Transporter 2
  • Glucagon-Like Peptide 1

Grants and funding

This research was funded by the Comunidad de Madrid in Plurianual agreement with the Universidad Rey Juan Carlos “Estímulo a la investigación de jóvenes doctores” program, grant number A484 (EXOKID) to RVB, Ministerio de Economía y Competitividad (Spain) (BFU2016-78951-R), Comunidad de Madrid (Spain) (S2017/BMD-3684), Ministerio de Ciencia e Innovación (Spain) (PID2020-116875RB-I00, PDC2021-121871-I00) to GMG.