» Articles » PMID: 38428428

Therapeutic Benefit of Idebenone in Patients with Leber Hereditary Optic Neuropathy: The LEROS Nonrandomized Controlled Trial

Abstract

Leber hereditary optic neuropathy (LHON) is a mitochondrial disease leading to rapid and severe bilateral vision loss. Idebenone has been shown to be effective in stabilizing and restoring vision in patients treated within 1 year of onset of vision loss. The open-label, international, multicenter, natural history-controlled LEROS study (ClinicalTrials.gov NCT02774005) assesses the efficacy and safety of idebenone treatment (900 mg/day) in patients with LHON up to 5 years after symptom onset (N = 199) and over a treatment period of 24 months, compared to an external natural history control cohort (N = 372), matched by time since symptom onset. LEROS meets its primary endpoint and confirms the long-term efficacy of idebenone in the subacute/dynamic and chronic phases; the treatment effect varies depending on disease phase and the causative mtDNA mutation. The findings of the LEROS study will help guide the clinical management of patients with LHON.

Citing Articles

Mitochondria-associated non-coding RNAs and their impact on drug resistance.

An X, Sun L, Zheng H, Xiao Y, Sun W, Yu D Front Pharmacol. 2025; 16:1472804.

PMID: 40078288 PMC: 11897306. DOI: 10.3389/fphar.2025.1472804.


Leber's hereditary optic neuropathy - current status of idebenone and gene replacement therapies.

Klopstock T, Zeng L, Priglinger C Med Genet. 2025; 37(1):57-63.

PMID: 39963374 PMC: 11831234. DOI: 10.1515/medgen-2024-2066.


The value of genetic testing in pediatric and adult ophthalmology.

Kellner U, Kellner S, Weinitz S, Farmand G Med Genet. 2025; 37(1):11-18.

PMID: 39963372 PMC: 11831236. DOI: 10.1515/medgen-2024-2059.


Mitochondrial diseases: from molecular mechanisms to therapeutic advances.

Wen H, Deng H, Li B, Chen J, Zhu J, Zhang X Signal Transduct Target Ther. 2025; 10(1):9.

PMID: 39788934 PMC: 11724432. DOI: 10.1038/s41392-024-02044-3.


Insights on the Genetic and Phenotypic Complexities of Optic Neuropathies.

DEsposito F, Zeppieri M, Cordeiro M, Capobianco M, Avitabile A, Gagliano G Genes (Basel). 2025; 15(12.

PMID: 39766826 PMC: 11675667. DOI: 10.3390/genes15121559.


References
1.
Liang M, Jiang P, Li F, Zhang J, Ji Y, He Y . Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy. Invest Ophthalmol Vis Sci. 2014; 55(3):1321-31. DOI: 10.1167/iovs.13-13011. View

2.
Carelli V, Carbonelli M, de Coo I, Kawasaki A, Klopstock T, Lagreze W . International Consensus Statement on the Clinical and Therapeutic Management of Leber Hereditary Optic Neuropathy. J Neuroophthalmol. 2017; 37(4):371-381. DOI: 10.1097/WNO.0000000000000570. View

3.
Kaiser P . Prospective evaluation of visual acuity assessment: a comparison of snellen versus ETDRS charts in clinical practice (An AOS Thesis). Trans Am Ophthalmol Soc. 2010; 107:311-24. PMC: 2814576. View

4.
Jaber S, Ge S, Milstein J, VanRyzin J, Waddell J, Polster B . Idebenone Has Distinct Effects on Mitochondrial Respiration in Cortical Astrocytes Compared to Cortical Neurons Due to Differential NQO1 Activity. J Neurosci. 2020; 40(23):4609-4619. PMC: 7275857. DOI: 10.1523/JNEUROSCI.1632-17.2020. View

5.
Newman N, Yu-Wai-Man P, Biousse V, Carelli V . Understanding the molecular basis and pathogenesis of hereditary optic neuropathies: towards improved diagnosis and management. Lancet Neurol. 2022; 22(2):172-188. DOI: 10.1016/S1474-4422(22)00174-0. View