Identifying and interpreting novel targets that address more than one diabetic complication: A strategy for optimal end organ protection in diabetes

Shinji Hagiwara, Jay C. Jha, Mark E. Cooper

Research output: Contribution to journalArticleOtherpeer-review

2 Citations (Scopus)

Abstract

It is increasingly appreciated that subjects with diabetes who develop one vascular complication are more likely to also suffer from another complication. For example, those with diabetic nephropathy will often have concomitant retinopathy and a much higher risk of macrovascular disease leading to increased cardiovascular morbidity and mortality. It is considered that haemodynamic and metabolic factors interact to activate signaling pathways that then result in upregulation of a range of well-characterized cytokines and growth factors leading to various pathological processes including angiogenesis, inflammation and extracellular matrix accumulation. As the various mediators of end-organ injury in diabetes are identified, new targets for intervention are being explored. Some of these targets such as enzymes implicated in oxidative stress such as nicotinamide adenine dinucleotide phosphate oxidase (Nox) 1 and Nox 4, various growth factors such as transforming growth factor-β (TGF-β) and vascular endothelial growth factor (VEGF) as well as their cognate receptors are increasingly being investigated first in preclinical studies and now in early phase clinical trials.

Original languageEnglish
Pages (from-to)1-20
Number of pages20
JournalDiabetology International
Volume5
Issue number1
DOIs
Publication statusPublished - 2014
Externally publishedYes

Keywords

  • AGEs
  • Diabetic complications
  • Diabetic nephropathy
  • Diabetic neuropathy
  • Diabetic retinopathy
  • Growth factors
  • Oxidative stress
  • PKC
  • Renin-angiotensin-aldosterone system
  • ROCK

Cite this