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Retinal layer thinning predicts treatment failure in relapsing multiple sclerosis.
Gabriel Bsteh1, Harald Hegen2, Patrick Altmann1
1Department of Neurology, Medical University of Vienna, Vienna, Austria.
Macular ganglion cell layer thinning predicts disease-modifying treatment failure in relapsing multiple sclerosis (RMS) patients. This finding offers a new biomarker for monitoring treatment effectiveness and guiding therapeutic decisions in RMS.
Area of Science:
- Ophthalmology
- Neurology
- Biomarkers
Background:
- Peripapillary retinal nerve fiber layer (pRNFL) and macular ganglion cell plus inner plexiform layer (GCIPL) thinning are indicators of neuroaxonal damage in multiple sclerosis (MS).
- Disease-modifying treatments (DMTs) can slow this degeneration.
Purpose of the Study:
- To assess the predictive value of pRNFL and GCIPL thinning for DMT failure in relapsing MS (RMS).
Main Methods:
- A 4-year prospective observational study involving 113 RMS patients.
- pRNFL and GCIPL were measured at DMT initiation and at 12 (M12) and 24 (M24) months.
- Treatment failure was defined by confirmed Expanded Disability Status Scale (EDSS) progression and/or Symbol Digit Modalities Test (SDMT) worsening.
Main Results:
- GCIPL thinning >0.5 μm/year at M24 was a strong predictor of treatment failure (HR: 4.5, p < 0.001).
- GCIPL thinning >0.5 μm at M12 also predicted failure (OR: 3.9, p < 0.001).
- pRNFL thinning ≥2 μm/year at M24 showed predictive value (OR: 3.7, p = 0.023), but pRNFL at M12 did not.
Conclusions:
- GCIPL thinning, and to a lesser extent pRNFL thinning, can predict disability progression following DMT initiation in RMS.
- These retinal layer measurements may serve as accessible biomarkers for predicting DMT failure in RMS.
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