Small-molecule modulation of ppars for the treatment of prevalent vascular retinal diseases

Xiaozheng Dou, Adam S. Duerfeldt

Research output: Contribution to journalReview articlepeer-review

7 Scopus citations


Vascular-related retinal diseases dramatically impact quality of life and create a substantial burden on the healthcare system. Age-related macular degeneration, diabetic retinopathy, and retinopathy of prematurity are leading causes of irreversible blindness. In recent years, the scientific community has made great progress in understanding the pathology of these diseases and recent discoveries have identified promising new treatment strategies. Specifically, compelling biochemical and clinical evidence is arising that small-molecule modulation of peroxisome proliferator-activated receptors (PPARs) represents a promising approach to simultaneously address many of the pathological drivers of these vascular-related retinal diseases. This has excited academic and pharmaceutical researchers towards developing new and potent PPAR ligands. This review highlights recent developments in PPAR ligand discovery and discusses the downstream effects of targeting PPARs as a therapeutic approach to treating retinal vascular diseases.

Original languageEnglish (US)
Article number9251
Pages (from-to)1-22
Number of pages22
JournalInternational journal of molecular sciences
Issue number23
StatePublished - Dec 1 2020

Bibliographical note

Funding Information:
Funding: This work was supported by the National Eye Institute of the National Institutes of Health under award numbers R21EY028279 (A.S.D.) and R01EY030472 (A.S.D.).

Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.


  • Age-related macular degeneration
  • Diabetic retinopathy
  • Drug discovery
  • Peroxisome proliferator-activated receptor
  • Retinopathy of prematurity


Dive into the research topics of 'Small-molecule modulation of ppars for the treatment of prevalent vascular retinal diseases'. Together they form a unique fingerprint.

Cite this