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Updated: Feb 1, 2026

Tear-Derived Exosomal miR-15a as New Diagnostic Tool for Diabetic Retinopathy
Published on: December 30, 2025
A non-invasive, multi-target approach to treat diabetic retinopathy
Angeline Julius1, Waheeta Hopper1
1Department of Biotechnology, School of Bioengineering, Faculty of Engineering and Technology, SRM Institute of Science and Technology, Chennai 603 203, India.
Abstract:
Hyperglycemia invoke number of pathways resulting in development of diabetic retinopathy (DR), including protein kinase C activation, increased expression of VEGF, advanced glycation end product (AGEs) formation and activation of polyol pathway, among which the pathophysiology of aldose reductase (ALR2) of the polyol pathway is evident by more than a decade of research. Subtle involvement of ALR2 in invoking various pathways of diabetic complications has caused an increase in attention towards the identification of novel aldose reductase inhibitors (ARIs). Numerous ARIs of different classes were employed in the treatment of diabetic complications initially, but few came into light as drugs. Though no ALR2 inhibitor has been used for the treatment or control of DR, Epalrestat has been used worldwide for treating diabetic neuropathy. This review critically analyses different treatments available for diabetic retinopathy, their limitations and the importance of the development of novel inhibitors of ALR2 that could prevent progression of DR, by causing a direct or indirect effect on controlling factors associated with DR.
Insights
Diabetic retinopathy (DR) involves pathways like aldose reductase (ALR2). Developing new ALR2 inhibitors could prevent DR progression, offering a novel therapeutic strategy.
Area of Science:
- Biochemistry
- Pharmacology
- Ophthalmology
Background:
- Hyperglycemia triggers pathways like protein kinase C activation, VEGF expression, AGEs formation, and polyol pathway activation, contributing to diabetic retinopathy (DR).
- Aldose reductase (ALR2) within the polyol pathway plays a significant role in diabetic complications, with its pathophysiology extensively researched.
- While numerous aldose reductase inhibitors (ARIs) have been explored, few have reached clinical use, and none are approved for DR treatment.
Purpose of the Study:
- To critically analyze current treatments for diabetic retinopathy (DR).
- To identify the limitations of existing DR therapies.
- To highlight the importance of developing novel aldose reductase inhibitors (ALR2 inhibitors) for preventing DR progression.
Main Methods:
- Literature review of existing treatments for diabetic retinopathy.
- Analysis of the role of aldose reductase (ALR2) in diabetic complications.
- Evaluation of the potential of aldose reductase inhibitors (ARIs) in managing DR.
Main Results:
- Several pathways contribute to DR, with ALR2 involvement being a key focus.
- Epalrestat, an ALR2 inhibitor, is used for diabetic neuropathy but not approved for DR.
- Existing treatments for DR have limitations, underscoring the need for new therapeutic approaches.
Conclusions:
- Novel aldose reductase inhibitors (ALR2 inhibitors) hold promise for preventing diabetic retinopathy (DR) progression.
- Targeting ALR2 could offer a direct or indirect mechanism to control factors implicated in DR.
- Further research into ALR2 inhibitors is crucial for developing effective DR treatments.
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