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Peripapillary retinal nerve fibre layer thinning rate as a biomarker discriminating stable and progressing relapsing-remitting multiple sclerosis.
Bsteh, G; Hegen, H; Teuchner, B; Berek, K; Wurth, S; Auer, M; Di Pauli, F; Deisenhammer, F; Berger, T.
Afiliación
  • Bsteh G; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Hegen H; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Teuchner B; Department of Ophthalmology, Medical University of Innsbruck, Innsbruck, Austria.
  • Berek K; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Wurth S; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Auer M; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Di Pauli F; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Deisenhammer F; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
  • Berger T; Department of Neurology, Medical University of Innsbruck, Innsbruck, Austria.
Eur J Neurol ; 26(6): 865-871, 2019 06.
Article en En | MEDLINE | ID: mdl-30614590
ABSTRACT
BACKGROUND AND

PURPOSE:

Peripapillary retinal nerve fibre layer (pRNFL) thickness is a strong candidate as a biomarker of axonal degeneration in multiple sclerosis (MS). The aim was to determine a cut-off value of pRNFL thinning rates in relapsing-remitting MS (RRMS) to discriminate between stable and progressing patients.

METHODS:

In this 3-year prospective longitudinal study on 141 RRMS patients, annual pRNFL thinning rates (aLpRNFL) were determined by individual linear regression models. The best possible cut-off value discriminating clinically progressing (physical progression or cognitive decline) and stable patients was defined by receiver operating characteristic analysis. Cut-off values were validated using a multivariate logistic regression model.

RESULTS:

Average aLpRNFL in progressing patients (2.4 µm, SD 2.1) was significantly higher compared to stable patients (0.5 µm, SD 1.2, P < 0.001). At a predefined specificity of 90%, aLpRNFL >1.5 µm was able to distinguish between stable and progressing RRMS with a sensitivity of 76.1%. aLpRNFL >1.5 µm was associated with a 15-fold increased risk of clinically progressing MS (P < 0.001).

CONCLUSIONS:

A cut-off of aLpRNFL discriminating clinically progressing and stable RRMS was identified. After validation in independent cohorts, this cut-off could be used as a biomarker of axonal degeneration supporting disease monitoring in daily clinical routine.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Retina / Esclerosis Múltiple Recurrente-Remitente Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Retina / Esclerosis Múltiple Recurrente-Remitente Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Año: 2019 Tipo del documento: Article