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Interactions of optic radiation lesions with retinal and brain atrophy in early multiple sclerosis

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Item Type:Article
Title:Interactions of optic radiation lesions with retinal and brain atrophy in early multiple sclerosis
Creators Name:Lin, T.Y. and Chien, C. and Kuchling, J. and Asseyer, S. and Motamedi, S. and Bellmann-Strobl, J. and Schmitz-Hübsch, T. and Ruprecht, K. and Brandt, A.U. and Zimmermann, H.G. and Paul, F.
Abstract:OBJECTIVE: Retrograde trans-synaptic neuroaxonal degeneration is considered a key pathological factor of subclinical retinal neuroaxonal damage in multiple sclerosis (MS). We aim to evaluate the longitudinal association of optic radiation (OR) lesion activity with retinal neuroaxonal damage and its role in correlations between retinal and brain atrophy in people with clinically isolated syndrome and early MS (pweMS). METHODS: Eighty-five pweMS were retrospectively screened from a prospective cohort (Berlin CIS cohort). Participants underwent 3T magnetic resonance imaging (MRI) for OR lesion volume and brain atrophy measurements and optical coherence tomography (OCT) for retinal layer thickness measurements. All pweMS were followed with serial OCT and MRI over a median follow-up of 2.9 (interquartile range: 2.6-3.4) years. Eyes with a history of optic neuritis prior to study enrollment were excluded. Linear mixed models were used to analyze the association of retinal layer thinning with changes in OR lesion volume and brain atrophy. RESULTS: Macular ganglion cell-inner plexiform layer (GCIPL) thinning was more pronounced in pweMS with OR lesion volume increase during follow-up compared to those without (Difference: -0.82 μm [95% CI:-1.49 to -0.15], p = 0.018). Furthermore, GCIPL thinning correlated with both OR lesion volume increase (β [95% CI] = -0.27 [-0.50 to -0.03], p = 0.028) and brain atrophy (β [95% CI] = 0.47 [0.25 to 0.70], p < 0.001). Correlations of GCIPL changes with brain atrophy did not differ between pweMS with or without OR lesion increase (η(2)(p) = 5.92e(-7), p = 0.762). INTERPRETATION: Faster GCIPL thinning rate is associated with increased OR lesion load. Our results support the value of GCIPL as a sensitive biomarker reflecting both posterior visual pathway pathology and global brain neurodegeneration.
Keywords:Atrophy, Central Nervous System Diseases, Multiple Sclerosis, Prospective Studies, Retinal Ganglion Cells, Retrospective Studies
Source:Annals of Clinical and Translational Neurology
Page Range:45-56
Date:January 2024
Official Publication:https://doi.org/10.1002/acn3.51931
PubMed:View item in PubMed

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