Diabetic nephropathy: An update on pathogenesis and drug development.


Journal

Diabetes & metabolic syndrome
ISSN: 1878-0334
Titre abrégé: Diabetes Metab Syndr
Pays: Netherlands
ID NLM: 101462250

Informations de publication

Date de publication:
Historique:
received: 06 11 2018
accepted: 29 11 2018
entrez: 16 1 2019
pubmed: 16 1 2019
medline: 26 4 2019
Statut: ppublish

Résumé

Diabetic nephropathy (DN) is a major cause of end-stage renal disease and affects a large number of individuals with diabetes. However, the development of specific treatments for DN has not yet been identified. Hence, this review is concisely designed to understand the molecular pathways leading to DN in order to develop suitable therapeutic strategies. Extensive literature search have been carried in regard with the pathogenesis and pathophysiology of DN, drug targets and updates on clinical trials, the consequences associated with DN and the potential biomarkers for diagnosis and prediction of DN are discussed in this review. DN is characterised by microalbuminuria and macroalbuminuria, and morphological changes such as glomerular thickening, interstitial fibrosis, formation of nodular glomerulosclerosis and decreased endothelial cell fenestration. Besides, the involvement of renin-angiotensin-aldosterone system, inflammation and genetic factors are the key pathways in the progression of DN. In regard with drug development drugs targeted to epidermal growth factor, inflammatory cytokines, ACTH receptor and TGFβ1 receptors are in pipeline for clinical trials whereas, several drugs have also failed in phase III and phase IV of clinical trials due to lack of efficacy and severe adverse effect. The research on DN is limited with respect to its pathogenesis and drug development. Thus, a more detailed understanding of the pathogenesis of DN is very essential to progress in the drug development process.

Identifiants

pubmed: 30641802
pii: S1871-4021(18)30527-7
doi: 10.1016/j.dsx.2018.11.054
pii:
doi:

Substances chimiques

Dipeptidyl-Peptidase IV Inhibitors 0
Inflammation Mediators 0
Sodium-Glucose Transporter 2 Inhibitors 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

754-762

Informations de copyright

Copyright © 2018 Diabetes India. Published by Elsevier Ltd. All rights reserved.

Auteurs

Vikram Rao A/L B Vasanth Rao (VR)

School of Postgraduate Studies, International Medical University, No 126, Jalan Jalil Perkasa 19, Bukit Jalil, 57000, Kuala Lumpur, Malaysia. Electronic address: Vikram.rao@studentimuedu.onmicrosoft.com.

Sean Hong Tan (SH)

School of Pharmacy, International Medical University, No 126, Jalan Jalil Perkasa 19, Bukit Jalil, 57000, Kuala Lumpur, Malaysia. Electronic address: Tan.SeanHong@student.imu.edu.my.

Mayuren Candasamy (M)

Department of Life Sciences, School of Pharmacy, International Medical University, No 126, Jalan Jalil Perkasa 19, Bukit Jalil, 57000, Kuala Lumpur, Malaysia. Electronic address: MayurenCandasamy@imu.edu.my.

Subrat Kumar Bhattamisra (SK)

Department of Life Sciences, School of Pharmacy, International Medical University, No 126, Jalan Jalil Perkasa 19, Bukit Jalil, 57000, Kuala Lumpur, Malaysia. Electronic address: subratkumar@imu.edu.my.

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Classifications MeSH