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[Memantine for optic nerve atrophy in Friedreich's Ataxia]
S Peter1, K Manousaridis2, S Boesch3
1Abteilung für Augenheilkunde, Akademisches Lehrkrankenhaus Feldkirch, Carinagasse 47, 6800, Feldkirch, Österreich. Silvia.Peter@Lkhf.at.
Memantine, an N-methyl-D-aspartate (NMDA) antagonist, may help preserve vision in Friedreich's ataxia patients experiencing optic nerve atrophy. A single case study showed stable visual acuity and nerve fiber layer thickness after one year of treatment.
Area of Science:
- Neuro-ophthalmology
- Neurodegenerative Diseases
- Pharmacology
Background:
- Friedreich's ataxia (FA) is a rare inherited disorder.
- Optic nerve atrophy leading to visual loss is a common complication in FA.
- Current treatment options for optic nerve atrophy in FA are limited.
Observation:
- A 24-year-old patient with FA presented with significant visual impairment due to optic nerve atrophy.
- The patient received off-label treatment with memantine, an N-methyl-D-aspartate (NMDA) receptor antagonist.
- Treatment was initiated after interdisciplinary consultation and informed consent.
Findings:
- A 1-year follow-up using optical coherence tomography (OCT) revealed no further loss of the nerve fiber layer.
- The patient's visual acuity remained stable throughout the follow-up period.
- This suggests a potential neuroprotective effect of memantine in this context.
Implications:
- Memantine may be a viable therapeutic option for managing acute optic nerve atrophy in Friedreich's ataxia.
- Further research, including larger studies, is warranted to confirm these preliminary findings.
- This case highlights the importance of considering novel therapeutic strategies for rare neurodegenerative conditions.
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