Evidence map›Paper›PMID 32368758›Full record

ArticleJournal of cellular immunology2020

Naltrexone as a Novel Therapeutic for Diabetic Corneal Complications.

Patricia J McLaughlin, Joseph W Sassani, Ian S Zagon

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Systemic diseases and the cornea.Experimental eye research · 2021
    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 1 institution in 1 country.

Patricia J McLaughlinDepartment of Neural and Behavioral Sciences, Penn State University College of Medicine, Hershey, Pennsylvania, 17033, USA.
Joseph W SassaniDepartment of Ophthalmology, Penn State University College of Medicine, Hershey, Pennsylvania, 17033, USA.
Ian S ZagonDepartment of Neural and Behavioral Sciences, Penn State University College of Medicine, Hershey, Pennsylvania, 17033, USA.
Penn State Milton S. Hershey Medical Center · US

Funding

OGF-OGFr Axis Modulation to Prevent Diabetic Ocular Surface Complications.R01EY029223 · NEI · PENNSYLVANIA STATE UNIV HERSHEY MED CTR · PI ZAGON, IAN S · 2018 to 2021
$1.5M
NEI NIH HHS R01 EY029223
6 · The paper itself

Abstract

Diabetes is a widespread autoimmune disorder that affects nearly 10% of the adult population in the United States. In addition to the primary disease, there are numerous complications associated with inflammation including abnormalities of the heart, visual system, and peripheral nervous system. More than half of the individuals with diabetes will have one or more ocular related complications such as dry eye disease (DED), keratopathy, or retinopathy. Research over the last 3 decades has focused on the role of the opioid growth factor - opioid growth factor receptor (OGF-OGFr) axis as a regulatory system that maintains homeostasis in corneal epithelialization and tear secretion. In diabetes, OGF appears to be dysregulated resulting in decreased cell replication and increased corneal surface sensitivity. Utilization of naltrexone as a topical therapeutic to block the OGF-OGFr axis results in reversal of dry eye and restoration of corneal sensitivity and rates of corneal re-epithelialization. Naltrexone treatment at dosages that are substantially lower than systemically approved doses appear to be safe and effective therapy for corneal surface abnormalities associated with diabetes.

Indexed as

Corneal surface abnormalitiesDiabetesDry eyeNaltrexone

Identifiers

PMID32368758
PMCPMC7198040
OpenAlexW3017590372

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.