Multifocal Electroretinogram Photopic Negative Response: A Reliable Paradigm to Detect Localized Retinal Ganglion Cells' Impairment in Retrobulbar Optic Neuritis Due to Multiple Sclerosis as a Model of Retinal Neurodegeneration.

multifocal electroretinogram multiple sclerosis neurodegeneration photopic negative response retinal ganglion cells

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
06 May 2022
Historique:
received: 29 03 2022
revised: 28 04 2022
accepted: 05 05 2022
entrez: 28 5 2022
pubmed: 29 5 2022
medline: 29 5 2022
Statut: epublish

Résumé

The measure of the full-field photopic negative response (ff-PhNR) of light-adapted full-field electroretinogram (ff-ERG) allows to evaluate the function of the innermost retinal layers (IRL) containing primarily retinal ganglion cells (RGCs) and other non-neuronal elements of the entire retina. The aim of this study was to acquire functional information of localized IRL by measuring the PhNR in response to multifocal stimuli (mfPhNR). In this case-control observational and retrospective study, we assessed mfPhNR responses from 25 healthy controls and from 20 patients with multiple sclerosis with previous history of optic neuritis (MS-ON), with full recovery of visual acuity, IRL morphological impairment, and absence of morpho-functional involvement of outer retinal layers (ORL). MfPhNR response amplitude densities (RADs) were measured from concentric rings (R) with increasing foveal eccentricity: 0−5° (R1), 5−10° (R2), 10−15° (R3), 15−20° (R4), and 20−25° (R5) from retinal sectors (superior-temporal (ST), superior-nasal (SN), inferior-nasal (IN), and inferior-temporal (IT)); between 5° and 20° and from retinal sectors (superior (S), temporal (T), inferior (I), and nasal (N)); and within 5° to 10° and within 10° and 20° from the fovea. The mfPhNR RAD values observed in all rings or sectors in MS-ON eyes were significantly reduced (p < 0.01) with respect to control ones. Our results suggest that mfPhNR recordings may detect localized IRL dysfunction in the pathologic condition of selective RGCs neurodegeneration.

Identifiants

pubmed: 35626311
pii: diagnostics12051156
doi: 10.3390/diagnostics12051156
pmc: PMC9139610
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Lucilla Barbano (L)

IRCCS-Fondazione Bietti, Via Livenza 1, 00198 Rome, Italy.

Lucia Ziccardi (L)

IRCCS-Fondazione Bietti, Via Livenza 1, 00198 Rome, Italy.

Giulio Antonelli (G)

IRCCS-Fondazione Bietti, Via Livenza 1, 00198 Rome, Italy.

Carolina Gabri Nicoletti (CG)

Multiple Sclerosis Clinical and Research Unit, Department of Systems Medicine, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy.

Doriana Landi (D)

Multiple Sclerosis Clinical and Research Unit, Department of Systems Medicine, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy.

Giorgia Mataluni (G)

Multiple Sclerosis Clinical and Research Unit, Department of Systems Medicine, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy.

Benedetto Falsini (B)

Ophthalmology Department, IRCCS-Fondazione Policlinico Universitario A. Gemelli, Catholic University, Largo F. Vito 1, 00168 Rome, Italy.

Girolama Alessandra Marfia (GA)

Multiple Sclerosis Clinical and Research Unit, Department of Systems Medicine, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy.

Diego Centonze (D)

Multiple Sclerosis Clinical and Research Unit, Department of Systems Medicine, Tor Vergata University, Via Montpellier 1, 00133 Rome, Italy.
Unit of Neurology and Neurorehabilitation, IRCCS-Neuromed, Via Atinense 18, 86077 Pozzilli, Italy.

Vincenzo Parisi (V)

IRCCS-Fondazione Bietti, Via Livenza 1, 00198 Rome, Italy.

Classifications MeSH