Evidence map›Paper›PMID 27102270›Full record

ReviewProgress in retinal and eye research2016

Aldose reductase, ocular diabetic complications and the development of topical Kinostat(®).

Peter F Kador, Milton Wyman, Peter J Oates

Open access · bronzeAbstract readReview
In one paragraph

Review in Progress in retinal and eye research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
5.5field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 2 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
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  10. Long-Term Diabetic Retinopathy Treatment Using Silicon Nanoneedles.Small (Weinheim an der Bergstrasse, Germany) · 2025
    Article
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  20. Current Approach to the Pathogenesis of Diabetic Cataracts.International journal of molecular sciences · 2023
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 2 institutions in 1 country.

Peter F KadorCollege of Pharmacy and Department of Ophthalmology, University of Nebraska Medical Center, Omaha, NE, USA; Therapeutic Vision, Inc., Omaha, NE, USA. Electronic address: pkador@unmc.edu.
Milton WymanTherapeutic Vision, Inc., Omaha, NE, USA; College of Veterinary Medicine, The Ohio State University, Columbus, OH, USA.
Peter J OatesOates Biomedical Consulting, LLC, Old Lyme, CT, USA.
Nebraska Medical Center · USTherapeutic Vision (United States) · US

Funding

Treatment of Canine Diabetic CataractsR44EY018013 · NEI · THERAPEUTIC VISION, INC. · PI WYMAN, MILTON NONE · 2010 to 2016
$2.4M
Investigating the Molecular Mechanism of Hexose-induced Stress in Lens and RetinaR01EY016730 · NEI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI KADOR, PETER F · 2006 to 2010
$1.6M
Treatment for Canine Diabetic CataractsR43EY018013 · NEI · THERAPEUTIC VISION, INC. · PI WYMAN, MILTON NONE · 2007 to 2007
$108k
NEI NIH HHS R01 EY016730NEI NIH HHS R43 EY018013NEI NIH HHS R44 EY018013
6 · The paper itself

Abstract

Diabetes mellitus (DM) is a major health problem with devastating effects on ocular health in both industrialized and developing countries. The control of hyperglycemia is critical to minimizing the impact of DM on ocular tissues because inadequate glycemic control leads to ocular tissue changes that range from a temporary blurring of vision to permanent vision loss. The biochemical mechanisms that promote the development of diabetic complications have been extensively studied. As a result, a number of prominent biochemical pathways have been identified. Among these, the two-step sorbitol pathway has been the most extensively investigated; nevertheless, it remains controversial. To date, long-term pharmacological studies in animal models of diabetes have demonstrated that the onset and development of ocular complications that include keratopathy, retinopathy and cataract can be ameliorated by the control of excess metabolic flux through aldose reductase (AR). Clinically the alleles of AR have been linked to the rapidity of onset and severity of diabetic ocular complications in diabetic patient populations around the globe. In spite of these promising preclinical and human genetic rationales, several clinical trials of varying durations with structurally diverse aldose reductase inhibitors (ARIs) have shown limited success or failure in preventing or arresting diabetic retinopathy. Despite these clinical setbacks, topical ARI Kinostat(®) promises to find a home in clinical veterinary ophthalmology where its anticipated approval by the FDA will present an alternative treatment paradigm to cataract surgery in diabetic dogs. Here, we critically review the role of AR in diabetes mellitus-linked ocular disease and highlight the development of Kinostat(®) for cataract prevention in diabetic dogs. In addition to the veterinary market, we speculate that with further safety and efficacy studies in humans, Kinostat(®) or a closely related product could have a future role in treating diabetic keratopathy.

Indexed as

Diabetes ComplicationsAdministration, TopicalAldehyde ReductaseAnimalsCataractCorneal DiseasesDiabetes MellitusDiabetic RetinopathyEnzyme InhibitorsHumansImidazolidinesOphthalmic SolutionsAldehyde ReductaseEnzyme InhibitorsImidazolidinesM 79175Ophthalmic SolutionsAldose reductase inhibitorDiabetic cataractDiabetic keratopathyDiabetic retinopathyKinostat(®)

Identifiers

PMID27102270
PMCPMC11844803
OpenAlexW2340637964

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.