Evidence map›Paper›PMID 42194266›Full record

ReviewBioengineering (Basel, Switzerland)2026

Retinal Ganglion Cell Degeneration in Glaucoma: Systematic Review.

Masuma Firoz, Neloy Shome, Noah Wong, Prisha Jonnalagadda, Hari Tunga, Amirmohammad Shafiee, Amirmahdi Shafiee, Sohan Bobba, Karanjit S Kooner

Abstract readReview
In one paragraph

Review in Bioengineering (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Association of FunctionalInternational journal of molecular sciences · 2026
    Article
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

9 authors.

Masuma FirozDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0009-0001-1567-1777
Neloy ShomeDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-3945-9279
Noah WongDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Prisha JonnalagaddaDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0009-0009-5520-8881
Hari TungaDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0009-0003-2978-4566
Amirmohammad ShafieeDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0009-0007-0483-8467
Amirmahdi ShafieeDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Sohan BobbaDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Karanjit S KoonerDepartment of Ophthalmology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.ORCID 0000-0002-2797-1750

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinal ganglion cell (RGC) degeneration underlies glaucomatous optic neuropathy and remains a leading cause of irreversible vision loss worldwide. Although elevated intraocular pressure (IOP) is the primary modifiable risk factor, RGC death reflects converging mechanisms including mechanical stress, vascular insufficiency, metabolic dysfunction, and neuroinflammation. We conducted a PRISMA-guided systematic review with PICOS-defined eligibility criteria, searching PubMed, Cochrane Library, ScienceDirect, Scopus, Google Scholar, and ProQuest for studies through January 2026 on RGC degeneration and neuroprotective or regenerative therapies in glaucoma. Included studies supported OCT-based structural assessment and imaging biomarkers as essential tools for early detection, risk stratification, and monitoring of progression and treatment response. Continued RGC loss despite IOP control in many patients highlights the need for mechanism-based interventions; neuroprotective strategies targeting excitotoxicity, oxidative stress, mitochondrial dysfunction, and neurotrophic insufficiency are emerging, while stem cell and gene-based regenerative therapies remain under active investigation. Integrating molecular insights with advanced imaging and biomarker-guided endpoints may enable earlier, more individualized intervention and help explain progression despite adequate pressure control.

Indexed as

artificial intelligenceglaucomaneurodegenerationneuroprotectionneuroregenerationretinal ganglion cells

Identifiers

PMID42194266
PMCPMC13203952

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.