Retinal layer thickness predicts disability accumulation in early relapsing multiple sclerosis

Author:

Bsteh Gabriel1ORCID,Hegen Harald2ORCID,Altmann Patrick1ORCID,Auer Michael2,Berek Klaus2ORCID,Di Pauli Franziska2ORCID,Haider Lukas3ORCID,Kornek Barbara1,Krajnc Nik1,Leutmezer Fritz1,Macher Stefan1ORCID,Rommer Paulus1ORCID,Walchhofer Lisa‐Maria4,Zebenholzer Karin1,Zulehner Gudrun1,Deisenhammer Florian2ORCID,Pemp Berthold5,Berger Thomas1

Affiliation:

1. Department of Neurology Medical University of Vienna Vienna Austria

2. Department of Neurology Medical University of Innsbruck Innsbruck Austria

3. Department of Neuroradiology Medical University of Vienna Vienna Austria

4. Department of Neuroradiology Medical University of Innsbruck Innsbruck Austria

5. Department of Ophthalmology Medical University of Vienna Vienna Austria

Abstract

AbstractBackground and purposeThis study was undertaken to investigate baseline peripapillary retinal nerve fiber layer (pRNFL) and macular ganglion cell and inner plexiform layer (GCIPL) thickness for prediction of disability accumulation in early relapsing multiple sclerosis (RMS).MethodsFrom a prospective observational study, we included patients with newly diagnosed RMS and obtained spectral‐domain optical coherence tomography scan within 90 days after RMS diagnosis. Impact of pRNFL and GCIPL thickness for prediction of disability accumulation (confirmed Expanded Disability Status Scale [EDSS] score ≥ 3.0) was tested by multivariate (adjusted hazard ratio [HR] with 95% confidence interval [CI]) Cox regression models.ResultsWe analyzed 231 MS patients (mean age = 30.3 years, SD = 8.1, 74% female) during a median observation period of 61 months (range = 12–93). Mean pRNFL thickness was 92.6 μm (SD = 12.1), and mean GCIPL thickness was 81.4 μm (SD = 11.8). EDSS ≥ 3 was reached by 28 patients (12.1%) after a median 49 months (range = 9–92). EDSS ≥ 3 was predicted with GCIPL < 77 μm (HR = 2.7, 95% CI = 1.6–4.2, p < 0.001) and pRNFL thickness ≤ 88 μm (HR = 2.0, 95% CI = 1.4–3.3, p < 0.001). Higher age (HR = 1.4 per 10 years, p < 0.001), incomplete remission of first clinical attack (HR = 2.2, p < 0.001), ≥10 magnetic resonance imaging (MRI) lesions (HR = 2.0, p < 0.001), and infratentorial MRI lesions (HR = 1.9, p < 0.001) were associated with increased risk of disability accumulation, whereas highly effective disease‐modifying treatment was protective (HR = 0.6, p < 0.001). Type of first clinical attack and presence of oligoclonal bands were not significantly associated.ConclusionsRetinal layer thickness (GCIPL more than pRNFL) is a useful predictor of future disability accumulation in RMS, independently adding to established markers.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference37 articles.

1. Multiple sclerosis

2. Disease-modifying treatments for early and advanced multiple sclerosis

3. Current therapeutic landscape in multiple sclerosis: an evolving treatment paradigm

4. Peripapillary retinal nerve fibre layer as measured by optical coherence tomography is a prognostic biomarker not only for physical but also for cognitive disability progression in multiple sclerosis;Bsteh G;Mult Scler J,2017

5. Macular ganglion cell–inner plexiform layer thinning as a biomarker of disability progression in relapsing multiple sclerosis [Internet];Bsteh G;Mult Scler J,2020

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