Evidence map›Paper›PMID 35038014›Full record

ReviewGraefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie2022

Differential susceptibility of retinal ganglion cell subtypes against neurodegenerative diseases.

Ningzhi Zhang, Xuejun He, Yiqiao Xing, Ning Yang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
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  7. Article
  8. Article
  9. Tunable dual-AAV sparse labeling of PVFrontiers in neural circuits · 2025
    Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Tools and Biomarkers for the Study of Retinal Ganglion Cell Degeneration.International journal of molecular sciences · 2022
    Review
  16. 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

4 authors at 1 institution in 1 country.

Ningzhi ZhangDepartment of Ophthalmology, Renmin Hospital of Wuhan University, Wuhan, China.
Xuejun HeDepartment of Ophthalmology, Renmin Hospital of Wuhan University, Wuhan, China.
Yiqiao XingDepartment of Ophthalmology, Renmin Hospital of Wuhan University, Wuhan, China.
Ning YangDepartment of Ophthalmology, Renmin Hospital of Wuhan University, Wuhan, China. rootyangning@whu.edu.cn.ORCID http://orcid.org/0000-0003-3036-0202
Wuhan University · CN

Funding

Fundamental Research Funds for the Central Universities 2042020kf0065Natural Science Foundation of Hubei Province 2020CFB240
6 · The paper itself

Abstract

Retinal ganglion cells (RGCs) are essential to propagate external visual information from the retina to the brain. Death of RGCs is speculated to be closely correlated with blinding retinal diseases, such as glaucoma and traumatic optic neuropathy (TON). Emerging innovative technologies have helped refine and standardize the classification of RGCs; at present, they are classified into more than 40 subpopulations in mammals. These RGC subtypes are identified by a combination of anatomical morphologies, electrophysiological functions, and genetic profiles. Increasing evidence suggests that neurodegenerative diseases do not collectively affect the RGCs. In fact, which RGC subtype exhibits the strongest or weakest susceptibility is hotly debated. Although a consensus has not yet been reached, it is certain that assorted RGCs display differential susceptibility against irreversible degeneration. Interestingly, a single RGC subtype can exhibit various vulnerabilities to optic nerve damage in diverse injury models. Thus, elucidating how susceptible RGC subtypes are to various injuries can protect vulnerable RGCs from damage and improve the possibility of preventing and treating visual impairment caused by neurodegenerative diseases. In this review, we summarize in detail the progress and status quo of research on the type-specific susceptibility of RGCs and point out current limitations and the possible directions for future research in this field.

Indexed as

GlaucomaNeurodegenerative DiseasesOptic Nerve InjuriesAnimalsDisease Models, AnimalHumansMammalsRetinal Ganglion CellsDifferential susceptibilityGlaucomaON/OFF pathwaysRetinal ganglion cell subtypesTraumatic optic neuropathy

Identifiers

PMID35038014
OpenAlexW4206562010

What OpenQuestion holds

Textmetadata
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.