Evidence map›Paper›PMID 36161379›Full record

ArticleDocumenta ophthalmologica. Advances in ophthalmology2022

Pattern ERGs suggest a possible retinal contribution to the visual acuity loss in acute optic neuritis.

I Kleerekooper, L Del Porto, L Dell'Arti, J Guajardo, S Leo, A G Robson, S A Trip, A Petzold, G T Plant, G E Holder

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In one paragraph

Article in Documenta ophthalmologica. Advances in ophthalmology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 9 citations in OpenAlex.

  1. Supernormal flicker ERG with postoperative CME after nDSAEK in bullous keratopathy.Documenta ophthalmologica. Advances in ophthalmology · 2026
    Article
  2. Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
    Article
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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 8 institutions in 6 countries.

I KleerekooperMoorfields Eye Hospital, City Road, London, UK. Iris.kleerekooper.18@ucl.ac.uk.ORCID 0000-0001-6456-9034
L Del PortoMoorfields Eye Hospital, City Road, London, UK.
L Dell'ArtiMoorfields Eye Hospital, City Road, London, UK.
J GuajardoMoorfields Eye Hospital, City Road, London, UK.
S LeoMoorfields Eye Hospital, City Road, London, UK.
A G RobsonMoorfields Eye Hospital, City Road, London, UK.
S A TripQueen Square MS CentreDepartment of Neuroinflammation, UCL Institute of Neurology, London, UK.
A PetzoldMoorfields Eye Hospital, City Road, London, UK.
G T Plant *Moorfields Eye Hospital, City Road, London, UK.
G E Holder *Moorfields Eye Hospital, City Road, London, UK.
Moorfields Eye Hospital · GBAmsterdam Neuroscience · NLFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITMoorfields Eye Hospital NHS Foundation Trust · GBNational Hospital for Neurology and Neurosurgery · GBNational University of Singapore · SGThe Royal Victorian Eye & Ear Hospital · AUUniversidad del Desarrollo · CL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMacular involvement in optic neuritis (ON) is well-recognised but poorly understood and may be of clinical relevance. This study explores macular structure-function correlates in acute ON.

methodsThis cross-sectional cohort study recruited ON patients within 14 days of symptom onset. Subjects underwent pattern electroretinography (PERG), pattern visual evoked potentials (PVEP) and optical coherence tomography (OCT) imaging. PERG P50 and N95 components were correlated with OCT data.

resultsTwenty-six individuals with ON were recruited, comprising eleven multiple sclerosis (MS-ON), six myelin oligodendrocyte glycoprotein associated (MOG-ON) and nine with isolated ON. These were compared with 28 healthy controls. PVEPs were undetectable in 11 (42%) of individuals with ON. When detectable, PVEP P100 was delayed (median 136 ms range 110-173 ms) and amplitude reduced (median 6 μV, range 3-14 μV) in ON compared with controls (both p < 0.001). PERG P50 component amplitudes, largely reflecting macular function, were reduced in affected eyes (median 2.3 μV; range 0.8-5.0 μV) compared with controls (3.3 μV; range 2.8-5.7 μV) and compared with fellow eyes (p < 0.001). The N95:P50 ratio was below the reference range in the affected eyes of five patients. Eight cases (32%) had subnormal P50 amplitudes (< 2.0 μV), and these patients had poorer visual acuity (p = 0.020). P50 amplitudes were positively correlated with an increase in inner nuclear layer thickness (r

conclusionPERG P50 component reduction reveals dysfunction of inner macular layers in acute ON and correlates with structural alterations on OCT. These early macular pathologic processes are likely to contribute to the visual loss.

Indexed as

ElectroretinographyOptic NeuritisCross-Sectional StudiesEvoked Potentials, VisualHumansTomography, Optical CoherenceVision DisordersVisual AcuityInner nuclear layer (INL)Macular functionMultiple sclerosisOptical coherence tomography (OCT)Optic neuritisPattern electroretinography (PERG)Pattern visual evoked potential (PVEP)

Identifiers

PMID36161379
OpenAlexW4297154050

What OpenQuestion holds

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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.