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Orphanet J Rare Dis. 2018 Feb 17;13(1):33. doi: 10.1186/s13023-018-0773-y.

Cyclosporine A does not prevent second-eye involvement in Leber's hereditary optic neuropathy.

Author information

Service d'Ophtalmologie, CHU Angers, 49000, Angers, France.
Institut MITOVASC, UMR CNRS 6015-INSERM1083, Université d'Angers, 49000, Angers, France.
Centre de référence des maladies neurogénétiques, Service de Neurologie, CHU Angers, 49000, Angers, France.
Unité Fonctionnelle d'Ophtalmologie, Centre de référence des Maladies Rares en Ophtalmologie OPHTARA, Hôpital Européen Georges Pompidou, Assistance Publique Hôpitaux de Paris, 75015, Paris, France.
Centre de compétence maladie rare, Clinique Jules Verne, 44300, Nantes, France.
Service d'Ophtalmologie, CHU de Bordeaux, 33000, Bordeaux, France.
Unité de Neuro-Ophtalmologie, Hospices Civils de Lyon, Hôpital Neurologique, 69677, Bron, France.
Service d'Ophtalmologie, CHU Angers, 49000, Angers, France.
Singapore Eye Research Institute, Singapore National Eye Centre and Duke-NUS, Singapore, Singapore.
Angers University Hospital, Angers, France.



Evaluation of the efficacy of oral cyclosporine A as a prophylactic agent in preventing second-eye involvement in Leber's hereditary optic neuropathy (LHON) in a prospective, open-label, non-randomized, multicenter pilot study. Only LHON patients aged 18 years or more, with confirmed primary mitochondrial DNA mutations and strictly unilateral optic neuropathy occurring within 6 months prior to enrolment, were included in the study. All these patients, receiving treatment with oral cyclosporine (Neoral®, Novartis) at 2.5 mg/kg/day, were examined at three-month intervals for a year. The primary endpoint was the best corrected visual acuity in the unaffected eye; the secondary endpoints were the best corrected visual acuity in the first eye affected, the mean visual field defect on automated perimetry, the thickness of the perifoveal retinal ganglion cell inner plexiform layer, and the thickness of the peripapillary retinal nerve fiber layer in both eyes.


Among the 24 patients referred to our institution with genetically confirmed LHON, between July 2011 and April 2014, only five patients, four males and one female, fulfilled the inclusion criteria. Age at enrolment ranged from 19 to 42 years (mean: 27.2 years; median: 26 years), four patients harbored the m.11778G > A pathogenic variant, and one the m.14484 T > C pathogenic variant. The time-interval between the onset of symptoms and inclusion in the study ranged from 7 to 17 weeks (mean: 11.8 weeks; median: 9 weeks). Despite treatment with oral cyclosporine A, all patients eventually experienced bilateral eye involvement, occurring within 11-65 weeks after the initiation of treatment. Over the study time period, the average best corrected visual acuity worsened in the first eye affected; by the end of the study, both eyes were equally affected.


Oral cyclosporine, at 2.5 mg/kg/day, did not prevent second-eye involvement in patients with strictly unilateral Leber's hereditary optic neuropathy.

TRIAL REGISTRATION: Identifier: NCT02176733 . Registrated June 25, 2014.


Cyclosporine; Leber’s hereditary optic neuropathy; Second-eye involvement

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