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dc.rights.licenseopenen_US
dc.contributor.authorLERUEZ, S.
dc.contributor.authorVERNY, C.
dc.contributor.authorBONNEAU, D.
dc.contributor.authorPROCACCIO, V.
dc.contributor.authorLENAERS, G.
dc.contributor.authorAMATI-BONNEAU, P.
dc.contributor.authorREYNIER, P.
dc.contributor.authorSCHERER, C.
dc.contributor.authorPRUNDEAN, A.
dc.contributor.authorORSSAUD, C.
dc.contributor.authorZANLONGHI, X.
hal.structure.identifierBordeaux population health [BPH]
dc.contributor.authorROUGIER, Marie-Benedicte
dc.contributor.authorTILIKETE, C.
dc.contributor.authorMILEA, D.
dc.date.accessioned2020-11-30T11:00:28Z
dc.date.available2020-11-30T11:00:28Z
dc.date.issued2018-02-17
dc.identifier.issn1750-1172 (Electronic) 1750-1172 (Linking)en_US
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/21257
dc.description.abstractEnBACKRGROUND: 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(R), 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. RESULTS: 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. CONCLUSIONS: 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: ClinicalTrials.gov Identifier: NCT02176733 . Registrated June 25, 2014.
dc.language.isoENen_US
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subject.enLEHA
dc.title.enCyclosporine A does not prevent second-eye involvement in Leber’s hereditary optic neuropathy
dc.title.alternativeOrphanet J Rare Disen_US
dc.typeArticle de revueen_US
dc.identifier.doi10.1186/s13023-018-0773-yen_US
dc.subject.halSciences du Vivant [q-bio]/Santé publique et épidémiologieen_US
dc.identifier.pubmed29454364en_US
bordeaux.page33en_US
bordeaux.volume13en_US
bordeaux.hal.laboratoriesBordeaux Population Health Research Center (BPH) - U1219en_US
bordeaux.issue1en_US
bordeaux.institutionUniversité de Bordeauxen_US
bordeaux.teamLEHA_BPH
bordeaux.peerReviewedouien_US
bordeaux.inpressnonen_US
hal.exportfalse
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.date=2018-02-17&rft.volume=13&rft.issue=1&rft.spage=33&rft.epage=33&rft.eissn=1750-1172%20(Electronic)%201750-1172%20(Linking)&rft.issn=1750-1172%20(Electronic)%201750-1172%20(Linking)&rft.au=LERUEZ,%20S.&VERNY,%20C.&BONNEAU,%20D.&PROCACCIO,%20V.&LENAERS,%20G.&rft.genre=article


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