Leber’s Hereditary Optic Neuropathy

Opinion statement

Leber’s hereditary optic neuropathy (LHON) is a maternally inherited blinding disease with variable penetrance. Three primary mitochondrial DNA mutations, affecting the respiratory complex I, are necessary but not sufficient to cause blindness. Reduced efficiency of ATP synthesis and increased oxidative stress are believed to sensitize the retinal ganglion cells to apoptosis. Different therapeutic strategies are considered to counteract this pathogenic mechanism. However, potential treatments for the visual loss are complicated by the fact that patients are unlikely to benefit after optic atrophy occurs. There is no proven therapy to prevent or reverse the optic neuropathy in LHON. Results from a recent trial with idebenone hold promise to limit neurodegeneration and improve final outcome, promoting recovery of visual acuity. Other therapeutic options are under scrutiny, including gene therapy, agents increasing mitochondrial biogenesis, and anti-apoptotic drugs.

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Correspondence to Chiara La Morgia MD.

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Sadun, A.A., Morgia, C.L. & Carelli, V. Leber’s Hereditary Optic Neuropathy. Curr Treat Options Neurol 13, 109–117 (2011). https://doi.org/10.1007/s11940-010-0100-y

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Keywords

  • Optical Coherence Tomography
  • Retinal Nerve Fiber Layer
  • Optic Neuropathy
  • Mitochondrial Permeability Transition Pore
  • Mitochondrial Permeability Transition Pore