Evidence map›Paper›PMID 33344053›Full record

ArticleTranslational vision science & technology2020

The Influence of Axial Length Upon the Retinal Ganglion Cell Layer of the Human Eye.

Min Chen, Jill Nofziger, Ritobrato Datta, James C Gee, Jessica Morgan, Geoffrey K Aguirre

Open access · goldAbstract read
In one paragraph

Article in Translational vision science & technology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Characterisation of the normal human ganglion cell-inner plexiform layer using widefield optical coherence tomography.Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) · 2024
    Article
  5. Article
  6. Prediction of visual field defects from macular optical coherence tomography in glaucoma using cluster analysis.Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) · 2022
    Article
  7. 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

6 authors at 3 institutions in 1 country.

Min ChenDepartment of Radiology, Scheie Eye Institute, Penn Presbyterian Medical Center, Philadelphia, PA, USA.
Jill NofzigerDepartment of Neurology, Scheie Eye Institute, Penn Presbyterian Medical Center, Philadelphia, PA, USA.
Ritobrato DattaDivision of Neurology, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
James C GeeDepartment of Radiology, Scheie Eye Institute, Penn Presbyterian Medical Center, Philadelphia, PA, USA.
Jessica MorganDepartment of Ophthalmology, Scheie Eye Institute, Penn Presbyterian Medical Center, Philadelphia, PA, USA.
Geoffrey K AguirreDepartment of Neurology, Scheie Eye Institute, Penn Presbyterian Medical Center, Philadelphia, PA, USA.
Penn Presbyterian Medical Center · USChildren's Hospital of Philadelphia · USUniversity of Pennsylvania · US

Funding

Scientific TransparencyP30EY001583 · NEI · UNIVERSITY OF PENNSYLVANIA · PI CLAIRE H MITCHELL · 1985 to 2026
$19.5M
Human Connectomes for Low Vision, Blindness, and Sight RestorationU01EY025864 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI AGUIRRE, GEOFFREY KARL, PATEL, VIVEK R. · 2015 to 2018
$4.0M
NEI NIH HHS P30 EY001583NEI NIH HHS U01 EY025864
6 · The paper itself

Abstract

Purpose: Variation in retinal thickness with eye size complicates efforts to estimate retinal ganglion cell number from optical coherence tomography (OCT) measures. We examined the relationship among axial length, the thickness and volume of the ganglion cell layer (GCL), and the size of the optic chiasm. Methods: We used OCT to measure GCL thickness over 50 degrees of the horizontal meridian in 50 healthy participants with a wide range of axial lengths. Using a model eye informed by individual biometry, we converted GCL thickness to tissue volume per square degree. We also measured the volume of the optic chiasm for 40 participants using magnetic resonance imaging (MRI). Results: There is a positive relationship between GCL tissue volume and axial length. Given prior psychophysical results, we conclude that increased axial length is associated with increased retinal ganglion cell size, decreased cell packing, or both. We characterize how retinal ganglion cell tissue varies systematically in volume and spatial distribution as a function of axial length. This model allows us to remove the effect of axial length from individual difference measures of GCL volume. We find that variation in this adjusted GCL volume correlates well with the size of the optic chiasm. Conclusions: Our results provide the volume of ganglion cell tissue in the retina, adjusted for the presumed effects of axial length upon ganglion cell size and/or packing. The resulting volume measure accounts for individual differences in the size of the optic chiasm, supporting its use to characterize the post-retinal visual pathway. Translational Relevance: Variations in ametropia can confound clinical measures of retinal features. We present a framework within which the thickness and volume of retinal structures can be measured and corrected for the effects of axial length.

Indexed as

Nerve FibersRetinal Ganglion CellsCross-Sectional StudiesHumansRetinaTomography, Optical Coherencemodel eyeoptical coherence tomographyretinal ganglion cellsspatial acuity

Identifiers

PMID33344053
PMCPMC7726585
OpenAlexW3112525246

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.