Optical coherence tomography as a biomarker of neurodegeneration in multiple sclerosis: A review

Neurodegeneration is one the most important pathological factors which contributes to permanent disability in multiple sclerosis (MS). Optical coherence tomography (OCT) measurements of macular ganglion cell layer (mGCL) and retinal nerve fiber layer (RNFL) have been proposed as biomarkers of axonal...

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Veröffentlicht in:Multiple sclerosis and related disorders 2018-05, Vol.22, p.77-82
Hauptverfasser: Alonso, Ricardo, Gonzalez-Moron, Dolores, Garcea, Orlando
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Sprache:eng
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Zusammenfassung:Neurodegeneration is one the most important pathological factors which contributes to permanent disability in multiple sclerosis (MS). Optical coherence tomography (OCT) measurements of macular ganglion cell layer (mGCL) and retinal nerve fiber layer (RNFL) have been proposed as biomarkers of axonal damage in MS. The aim of this review is to describe the most relevant findings regarding OCT and axonal damage in MS. We have selected studies that describe retina impairment in MS patients, and those which quantitatively assess the relationship between OCT and physical disability, cognitive impairment and relationship between OCT and magnetic resonance imaging (MRI). Results show that there is a relationship between the degree of retinal layers reduction and physical or cognitive disability and degenerative changes in MRI. •The aim of this studyis to make a review of optical coherence tomography (OCT) as a biomarker of neurodegeneration and axonal loss in multiple sclerosis (MS).•The use of neurodegeneration biomarkers could be a useful tool for monitoring patients during clinical practice and a measure of outcome in clinical trials.•Retinal nerve fiber layer (RNFL) and macular ganglion cell layer (mGGL) are affected by MS and are related to clinical and paraclinical parameters.•The results of the research suggest that changes in the retina measured by OCT are a marker of overall axonal loss and neurodegeneration.
ISSN:2211-0348
2211-0356
DOI:10.1016/j.msard.2018.03.007