Diabetic nephropathy: newer therapeutic perspectives.

J Community Hosp Intern Med Perspect

Department of Medicine, Division of Nephrology, Medical College of Wisconsin, Milwaukee, WI, USA.

Published: August 2018

AI Article Synopsis

  • Diabetic nephropathy (DN) is a major complication of diabetes, contributing to about 40% of end-stage renal disease (ESRD) and increasing cardiovascular risk.
  • Recent research has identified various pharmacological targets for DN treatment, highlighting the effectiveness of SGLT-2 inhibitors and exploring new pathways that address inflammation and oxidative damage.
  • Several promising drugs have entered human trials, with ongoing research aimed at improving clinical practices and treatment options for DN.

Article Abstract

Diabetic nephropathy (DN is a dreaded consequence of diabetes mellitus, accounting for about 40% of end-stage renal disease (ESRD). It is responsible for significant morbidity and mortality, both directly by causing ESRD and indirectly by increasing cardiovascular risk. Extensive research in this field has thrown light on multiple pathways that can be pharmacologically targeted, to control or reverse the process of DN. Glomerulocentric approach of DN still continues to produce favourable results as evidenced by the recent data on SGLT-2 (sodium glucose co-transporter type 2) inhibitors. Beyond the glomerular mechanisms, numerous novel pathways have been discovered in the last decade. Some of these pathways target inflammatory and oxidative damage, while the others target more specific mechanisms such as AGE-RAGE (advanced glycation end products-receptors for advanced glycation end products), ASK (apoptotic signal-regulating kinase), and endothelin-associated pathways. As a result of the research, a handful of clinically relevant drugs have made it to the human trials which have been elucidated in the following review, bearing in the mind that there are many more to come over the next few years. Ongoing research is expected to inform the clinicians regarding the use of the newer drugs in DN. USFDA: Unites States Food and Drug Administration; SGLT-2: Sodium glucose transporter type 2; GLP-1: Glucagon-like peptide-1; DDP-4: Dipeptidyl peptidase-4; UACR: urinary albumin creatinine ratio; eGFR: Estimated glomerular filtration rate; CKD: Chronic kidney disease; DN: Diabetic nephropathy; TGF: Tubuloglomerular feedback; RAAS: Renin angiotensin aldosterone system; T1DM: Type 1 diabetes mellitus; T2DM: Type 2 diabetes mellitus; RCT: Randomized controlled trial; AGE-RAGE: Advanced glycation end products-receptors for advanced glycation end products; ASK-1: Apoptotic signal-regulating kinase-1; Nrf-2: Nuclear 1 factor [erythroid derived-2]-related factor 2; ml/min/1.73m: Millilitre/minute/1.73 square meters of body surface area; ~: Approximately.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116149PMC
http://dx.doi.org/10.1080/20009666.2018.1500423DOI Listing

Publication Analysis

Top Keywords

advanced glycation
16
diabetic nephropathy
12
diabetes mellitus
12
sglt-2 sodium
8
sodium glucose
8
age-rage advanced
8
glycation products-receptors
8
products-receptors advanced
8
glycation products
8
apoptotic signal-regulating
8

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!