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1000 Titel
  • Leber’s hereditary optic neuropathy: course of disease in consideration of idebenone treatment and type of mutation
1000 Autor/in
  1. Tonagel, Felix |
  2. Wilhelm, Helmut |
  3. Richter, Paul |
  4. Kelbsch, Carina |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-12-18
1000 Erschienen in
1000 Quellenangabe
  • 259(4):1009-1013
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00417-020-05045-4 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8016777/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Purpose!#!In September 2015, the first and so far only medication for treatment of Leber's hereditary optic neuropathy (LHON) was approved in the EU. The drug in question is idebenone (©Raxone) and has been given to all newly diagnosed patients of the University Eye Hospital Tuebingen since the approval of the drug. The aim of the study was to find out whether regular administration of the drug led to an improvement in vision. We retrospectively examined 2 cohorts of consecutive patients with newly occurred visual impairment and LHON diagnosis: One with the initial diagnosis made from January 2010 until April 2014 and a second from October 2015 until January 2020.!##!Methods!#!Retrospective, observational cohort study. All electronic medical files of newly diagnosed and genetically confirmed LHON patients of the University Eye Hospital Tuebingen from January 2010 until April 2014 (cohort 1) and October 2015 until January 2020 (cohort 2) with at least 12 months of follow-up examinations have been analyzed.!##!Results!#!Five patients were included in the first and 7 patients in the second cohort. Patients of cohort 1 received no medication; patients of cohort 2, a daily dose of 900 mg idebenone. The primary visual acuity (VA) ranged between 0.03 and 0.5 in cohort 1 and did not improve during the observation period (median 60 months, range 23-87 months). The patients of cohort 2 have been observed for a median of 23 months (range 12-35 m). The primary VA ranged from 0.01 to 0.16. A recovery in one or both eyes with a final VA from 0.8 to 1.0 was experienced in 3 out of 7 patients. All patients showing a recovery of VA carried the m.11778G>A mutation.!##!Conclusion!#!The observed improvement in the treated cohort may be considered as a hint on the efficacy of idebenone in LHON. The time course of improvement suggests that idebenone should be given 1.5 years in newly diagnosed LHON cases.
1000 Sacherschließung
lokal 11778
lokal Mutation [MeSH]
lokal Ubiquinone/analogs
lokal DNA, Mitochondrial [MeSH]
lokal Humans [MeSH]
lokal Retrospective Studies [MeSH]
lokal Optic Atrophy, Hereditary, Leber/drug therapy [MeSH]
lokal Leber’s hereditary optic neuropathy
lokal Optic Atrophy, Hereditary, Leber/genetics [MeSH]
lokal LHON
lokal Idebenone
lokal Improvement
lokal Neuro-Ophthalmology
lokal Recovery
lokal Optic Atrophy, Hereditary, Leber/diagnosis [MeSH]
1000 Liste der Beteiligten
  1. https://orcid.org/0000-0002-5192-0347|https://frl.publisso.de/adhoc/uri/V2lsaGVsbSwgSGVsbXV0|https://frl.publisso.de/adhoc/uri/UmljaHRlciwgUGF1bA==|https://frl.publisso.de/adhoc/uri/S2VsYnNjaCwgQ2FyaW5h
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1000 Erstellt am 2023-11-17T10:49:41.952+0100
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