Pharmacotherapy to delay the progression of diabetic kidney disease in people with type 2 diabetes: past, present and future

Author:

Mallik Ritwika1,Chowdhury Tahseen A.2ORCID

Affiliation:

1. Department of Diabetes and Metabolism, The Royal London Hospital, London, UK

2. Department of Diabetes and Metabolism, The Royal London Hospital, 7th Floor, John Harrison House, Whitechapel, London E1 1BB, UK

Abstract

Diabetic kidney disease (DKD) is a leading cause of morbidity and mortality among people living with diabetes, and is one of the most important causes of end stage renal disease worldwide. In order to reduce progression of DKD, important management goals include treatment of hypertension, glycaemia and control of cardiovascular risk factors such as lipids, diet, smoking and exercise. Use of angiotensin converting enzyme inhibitors or angiotensin receptor blockers has an established role in prevention of progression of DKD. A number of other agents such as endothelin-1 receptor antagonists and bardoxolone have had disappointing results. Recent studies have, however, suggested that newer antidiabetic agents such as sodium-glucose transporter-2 inhibitors (SGLT-2i) and glucagon-like peptide-1 analogues have specific beneficial effects in patients with DKD. Indeed most recent guidance suggest that SGLT-2i drugs should be used early in DKD, irrespective of glucose control. A number of pathways are hypothesised for the development and progression of DKD, and have opened up a number of newer potential therapeutic targets. This article aims to discuss management of DKD with respect to seminal trials from the past, more recent trials informing the present and potential new therapeutic options that may be available in the future.

Publisher

SAGE Publications

Subject

Endocrinology, Diabetes and Metabolism

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