4.2 Review

Dipeptidyl peptidase-4 inhibitors in progressive kidney disease

Journal

CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION
Volume 24, Issue 1, Pages 67-73

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/MNH.0000000000000080

Keywords

diabetic nephropathy; DPP-4 inhibitor; GLP-1; incretin

Funding

  1. Astellas
  2. Astrazeneca
  3. Bristol Myers
  4. Boehringer Ingelheim
  5. Daiichi-Sankyo
  6. Eli lilly
  7. Kowa
  8. Kyowahakko-Kirin
  9. Mitsubishi-Tanabe
  10. MSD
  11. Novartis
  12. Novo Nordisk
  13. Ono
  14. Sanwa Kagaku
  15. Sanofi
  16. Takeda

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Purpose of review Dipeptidyl peptidase-4 (DPP-4) inhibitors are incretin-based drugs approved for the treatment of type 2 diabetes. The main action of DPP-4 inhibitors is to increase the level of incretin hormones such as glucagon-like peptide-1 (GLP-1), thereby stimulating insulin secretion from pancreatic beta cells. Recently emerging evidence suggests the pleiotropic extrapancreatic function of GLP-1 or DPP-4 inhibitors, including kidney and cardiovascular protection. Here, we review the effects of DPP-4 inhibitors on progressive kidney disease such as diabetic nephropathy from a therapeutic point of view. Recent findings A growing number of studies in animal models and human diseases have shown that DPP-4 inhibition ameliorates kidney disease by a process independent of glucose lowering. Possible mechanisms underlying such protective properties include the facilitation of natriuresis and reduction of blood pressure, and also local effects of the reduction of oxidative stress, inflammation and improvement of endothelial function in the kidney. DPP-4 inhibitors may also restore other DPP-4 substrates which have proven renal effects. Summary Treatment of diabetes with DPP-4 inhibitors is likely to involve a variety of extrapancreatic effects including renal protection. Such pleiotropic action of DPP-4 inhibitors might occur by both incretin-dependent and incretin-independent mechanisms. Conclusive evidence is needed to translate the favorable results from animal models to humans.

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