Predictive value of retinal atrophy for cognitive decline across disease duration in multiple sclerosis

dc.contributor.authorAlba Arbalat, Salut
dc.contributor.authorSolana Díaz, Elisabeth
dc.contributor.authorLópez Soley, Elisabet
dc.contributor.authorCamós Carreras, Anna
dc.contributor.authorMartinez de las Heras, Eloy
dc.contributor.authorVivó Pascual, Francesc
dc.contributor.authorPulido Valdeolivas, Irene
dc.contributor.authorAndorrà Ingles, Magí
dc.contributor.authorSepúlveda Gázquez, Maria
dc.contributor.authorCabrera Maqueda, Jose Maria
dc.contributor.authorFonseca, Elianet G.
dc.contributor.authorCalvi, Alberto
dc.contributor.authorAlcubierre, Rafel
dc.contributor.authorDotti Boada, Marina
dc.contributor.authorSaiz Hinarejos, Albert
dc.contributor.authorMartínez Lapiscina, Elena H.
dc.contributor.authorVilloslada Diaz, Pablo
dc.contributor.authorBlanco Morgado, Yolanda
dc.contributor.authorSánchez Dalmau, Bernardo
dc.contributor.authorLlufriu Duran, Sara
dc.date.accessioned2026-03-10T12:19:04Z
dc.date.available2026-03-10T12:19:04Z
dc.date.issued2024-05-01
dc.date.updated2026-03-09T14:02:20Z
dc.description.abstractBackground We investigated the association between changes in retinal thickness and cognition in people with MS (PwMS), exploring the predictive value of optical coherence tomography (OCT) markers of neuroaxonal damage for global cognitive decline at different periods of disease.Method We quantified the peripapillary retinal nerve fibre (pRFNL) and ganglion cell-inner plexiform (GCIPL) layers thicknesses of 207 PwMS and performed neuropsychological evaluations. The cohort was divided based on disease duration (<= 5 years or >5 years). We studied associations between changes in OCT and cognition over time, and assessed the risk of cognitive decline of a pRFNL <= 88 mu m or GCIPL <= 77 mu m and its predictive value.Results Changes in pRFNL and GCIPL thickness over 3.2 years were associated with evolution of cognitive scores, in the entire cohort and in patients with more than 5 years of disease (p<0.01). Changes in cognition were related to less use of disease-modifying drugs, but not OCT metrics in PwMS within 5 years of onset. A pRFNL <= 88 mu m was associated with earlier cognitive disability (3.7 vs 9.9 years) and higher risk of cognitive deterioration (HR=1.64, p=0.022). A GCIPL <= 77 mu m was not associated with a higher risk of cognitive decline, but a trend was observed at <= 91.5 mu m in PwMS with longer disease (HR=1.81, p=0.061).Conclusions The progressive retinal thinning is related to cognitive decline, indicating that cognitive dysfunction is a late manifestation of accumulated neuroaxonal damage. Quantifying the pRFNL aids in identifying individuals at risk of cognitive dysfunction.
dc.format.extent25 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idimarina9379830
dc.identifier.issn1468-330X
dc.identifier.pmid37989566
dc.identifier.urihttps://hdl.handle.net/2445/227969
dc.language.isoeng
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1136/jnnp-2023-332332
dc.relation.ispartofJournal of Neurology, Neurosurgery and Psychiatry, 2024, vol. 95, num. 5, p. 419-425
dc.relation.urihttps://doi.org/10.1136/jnnp-2023-332332
dc.rights(c) Alba Arbalat, Salut et al., 2024
dc.sourceArticles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
dc.subject.classificationTrastorns de l'atenció
dc.subject.classificationPacients amb lesions cerebrals
dc.subject.classificationOftalmopaties
dc.subject.otherAttention disorders
dc.subject.otherBrain damage patients
dc.subject.otherOphthalmopathies
dc.titlePredictive value of retinal atrophy for cognitive decline across disease duration in multiple sclerosis
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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