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Changes in Retinal OCT and Their Correlations with Neurological Disability in Early ALS Patients, a Follow-Up Study

dc.contributor.authorRojas Lozano, María Del Pilar
dc.contributor.authorHoz Montañana, María Rosa De
dc.contributor.authorRamírez Sebastián, Ana Isabel
dc.contributor.authorFerreras, Antonio
dc.contributor.authorGarcía Martín, Elena Salobrar
dc.contributor.authorMuñóz Blanco, José L
dc.contributor.authorUrcelay Segura, José Luis
dc.contributor.authorSalazar Corral, Juan José
dc.contributor.authorRamírez Sebastián, José Manuel
dc.date.accessioned2023-06-16T15:15:24Z
dc.date.available2023-06-16T15:15:24Z
dc.date.issued2019-12
dc.descriptionReceived: 14 October 2019 / Revised: 12 November 2019 / Accepted: 21 November 2019 / Published: 24 November 2019
dc.description.abstractBackground: To compare early visual changes in amyotrophic lateral sclerosis (ALS) patients with healthy controls in a baseline exploration, to follow-up the patients after 6 months, and to correlate these visual changes with neurological disability. Methods: All patients underwent a comprehensive neurological and ophthalmological examination. A linear mixed analysis and Bonferroni p-value correction were performed, testing four comparisons as follows: Control baseline vs. control follow-up, control baseline vs. ALS baseline, control follow-up vs. ALS follow-up, and ALS baseline vs. ALS follow-up. Results: The mean time from the diagnosis was 10.80 ± 5.5 months. The analysis of the optical coherence tomography (OCT) showed: (1) In ALS baseline vs. control baseline, a macular significantly increased thickness of the inner macular ring temporal and inferior areas; (2) in ALS follow-up vs. ALS baseline, a significant macular thinning in the inner and outer macular ring inferior areas; (3) in ALS follow-up vs. ALS baseline, a significant peripapillary retinal nerve fiber layer (pRNFL) thinning in the superior and inferior quadrants; and (4) ALS patients showed a moderate correlation between some OCT pRNFL parameters and Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised (ALSFRS-R) score. Conclusion: The OCT showed retinal changes in patients with motoneuron disease and could serve as a complementary tool for studying ALS.en
dc.description.departmentUnidad Docente de Inmunología, Oftalmología y ORL
dc.description.facultyFac. de Óptica y Optometría
dc.description.refereedTRUE
dc.description.statuspub
dc.eprint.idhttps://eprints.ucm.es/id/eprint/58011
dc.identifier.citationRojas Lozano, P., Hoz Montañana, M. R., Ramírez Sebastián, A. I. et al. «Changes in Retinal OCT and Their Correlations with Neurological Disability in Early ALS Patients, a Follow-Up Study». Brain Sciences, vol. 9, n.o 12, noviembre de 2019, p. 337. DOI.org (Crossref), https://doi.org/10.3390/brainsci9120337.
dc.identifier.doi10.3390/brainsci9120337
dc.identifier.issn2076-3425
dc.identifier.officialurlhttps://doi.org/10.3390/brainsci9120337
dc.identifier.relatedurlhttps://www.mdpi.com/2076-3425/9/12/337
dc.identifier.urihttps://hdl.handle.net/20.500.14352/5973
dc.issue.number12
dc.journal.titleBrain Sciences
dc.language.isoeng
dc.page.initialnº 337
dc.publisherMDPI AG
dc.rightsAtribución 3.0 España
dc.rights.accessRightsopen access
dc.rights.urihttps://creativecommons.org/licenses/by/3.0/es/
dc.subject.cdu616.832.522:611.843
dc.subject.cdu617.735-073.75
dc.subject.keywordALS
dc.subject.keywordAmyotrophic lateral sclerosis
dc.subject.keywordEje
dc.subject.keywordOCT
dc.subject.keywordOPtic nerve
dc.subject.keywordRetina
dc.subject.ucmNeurociencias (Medicina)
dc.subject.ucmAnatomía ocular
dc.subject.ucmTécnicas de la imagen
dc.subject.unesco2490 Neurociencias
dc.titleChanges in Retinal OCT and Their Correlations with Neurological Disability in Early ALS Patients, a Follow-Up Studyen
dc.typejournal article
dc.volume.number9
dspace.entity.typePublication
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relation.isAuthorOfPublication.latestForDiscovery96eaf4c7-e811-480b-86ef-b2c0c3274977

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