Evidence map›Paper›PMID 34643661›Full record

ArticleInvestigative ophthalmology & visual science2021

Localized Structural and Functional Deficits in a Nonhuman Primate Model of Outer Retinal Atrophy.

Ying V Liu, Gregory Konar, Kanza Aziz, Sai Bo Bo Tun, Candice Ho Ee Hua, Bingyao Tan, Jing Tian, Chi D Luu, Veluchamy A Barathi, Mandeep S Singh

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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  3. 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

10 authors at 5 institutions in 3 countries.

Ying V LiuWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
Gregory KonarWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
Kanza AzizWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
Sai Bo Bo TunSingapore Eye Research Institute, Singapore National Eye Center, Singapore, Singapore.
Candice Ho Ee HuaSingapore Eye Research Institute, Singapore National Eye Center, Singapore, Singapore.
Bingyao TanSingapore Eye Research Institute, Singapore National Eye Center, Singapore, Singapore.
Jing TianDepartment of Biostatistics, Johns Hopkins University Bloomberg School of Public Health, Baltimore, United States.
Chi D LuuCentre for Eye Research Australia, Royal Victorian Eye and Ear Hospital, Victoria, Australia.
Veluchamy A BarathiSingapore Eye Research Institute, Singapore National Eye Center, Singapore, Singapore.
Mandeep S SinghWilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, Maryland, United States.
Johns Hopkins University · USSingapore National Eye Center · SGCentre for Eye Research Australia · AUJohns Hopkins Medicine · USSingapore Eye Research Institute · SG

Funding

Wilmer Core Grant for Vision ResearchP30EY001765 · NEI · JOHNS HOPKINS UNIVERSITY · PI Jiang Qian · 1985 to 2026
$22.1M
Developing photoreceptor repair for macular degeneration therapy.R01EY033103 · NEI · JOHNS HOPKINS UNIVERSITY · PI SINGH, MANDEEP · 2021 to 2025
$2.0M
NEI NIH HHS P30 EY001765NEI NIH HHS R01 EY033103
6 · The paper itself

Abstract

Purpose: Cell-based therapy development for geographic atrophy (GA) in age-related macular degeneration (AMD) is hampered by the paucity of models of localized photoreceptor and retinal pigment epithelium (RPE) degeneration. We aimed to characterize the structural and functional deficits in a laser-induced nonhuman primate model, including an analysis of the choroid. Methods: Macular laser photocoagulation was applied in four macaques. Fundus photography, optical coherence tomography (OCT), dye angiography, and OCT-angiography were conducted over 4.5 months, with histological correlation. Longitudinal changes in spatially resolved macular dysfunction were measured using multifocal electroretinography (MFERG). Results: Lesion features, depending on laser settings, included photoreceptor layer degeneration, inner retinal sparing, skip lesions, RPE elevation, and neovascularization. The intralesional choroid was degenerated. The normalized mean MFERG amplitude within lesions was consistently lower than control regions (0.94 ± 0.35 vs. 1.10 ± 0.27, P = 0.032 at month 1, 0.67 ± 0.22 vs. 0.83 ± 0.15, P = 0.0002 at month 2, and 0.97 ± 0.31 vs. 1.20 ± 0.21, P < 0.0001 at month 3.5). The intertest variation of mean MFERG amplitudes in rings 1 to 5 ranged from 13.0% to 26.0% in normal eyes. Conclusions: Laser application in this model caused localized outer retinal, RPE, and choriocapillaris loss. Localized dysfunction was apparent by MFERG in the first month after lesion induction. Correlative structure-function testing may be useful for research on the functional effects of stem cell-based therapy for GA. MFERG amplitude data should be interpreted in the context of relatively high intertest variability of the rings that correspond to the central macula. Sustained choroidal insufficiency may limit long-term subretinal graft viability in this model.

Indexed as

AnimalsDisease Models, AnimalElectroretinographyFluorescein AngiographyFundus OculiGeographic AtrophyMacaca fascicularisRetinal Photoreceptor Cell Outer SegmentRetinal Pigment EpitheliumTomography, Optical CoherenceVisual Acuity

Identifiers

PMID34643661
PMCPMC8525844
OpenAlexW3205026936

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.