Journal Article DZNE-2026-01127

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Visual acuity changes in idebenone treatment‑naïve patients with Leber hereditary optic neuropathy: insights from the CRS-2 study.

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2026
Steinkopff [Darmstadt]

Journal of neurology 273(11), 690 () [10.1007/s00415-026-14181-6]

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Abstract: Case Record Survey (CRS)-2 was an international, multicenter, retrospective study designed to characterize the natural history of vision loss and spontaneous recovery in patients with Leber hereditary optic neuropathy (LHON).Case records of idebenone treatment-naïve patients aged ≥12 years, with mitochondrial DNA (mtDNA) variants m.3460G>A, m.11778G>A or m.14484 T>C, onset of symptoms (OoS) after 1999, and ≥2 visual acuity (VA) assessments within 5 years of OoS were analyzed. Disease phases were subacute/dynamic (≤1 year) or chronic (>1 year from OoS). Separate analyses were performed for eyes with VA assessments within 12 or 24±3 months from baseline (first VA assessment after OoS in each eye). Outcomes included: spontaneous clinically relevant recovery (sCRR; improvement from off-chart to ≤1.6 logMAR, or ≥0.2 logMAR if on-chart), sCR stabilization (sCRS; maintenance of VA <1.0 logMAR), sCR benefit (sCRB; eyes with a sCRR and/or sCRS), and sCR worsening (sCRW; worsening to off-chart, or loss of ≥0.2 logMAR if on-chart). The primary endpoint was the proportion of subacute/dynamic eyes 12 months from baseline with sCRB.Of 402 eligible eyes, 385 were subacute/dynamic at baseline, with 96 included in the 12-month analysis. Most patients were male (79.9%), with the m.11778G>A variant (71.7%). The primary endpoint was observed in 20.8% (n=20/96) of eyes. Spontaneous visual outcomes varied by disease phase, mtDNA variant, sex, and age at OoS.CRS-2 provides insights into LHON natural history and suggests the disease course may be more dynamic than previously reported, with spontaneous VA changes occurring well into the chronic phase.ClinicalTrials.gov NCT02796274, May 2016.

Keyword(s): Humans (MeSH) ; Optic Atrophy, Hereditary, Leber: physiopathology (MeSH) ; Optic Atrophy, Hereditary, Leber: drug therapy (MeSH) ; Optic Atrophy, Hereditary, Leber: genetics (MeSH) ; Male (MeSH) ; Female (MeSH) ; Ubiquinone: analogs & derivatives (MeSH) ; Ubiquinone: therapeutic use (MeSH) ; Ubiquinone: pharmacology (MeSH) ; Visual Acuity: physiology (MeSH) ; Visual Acuity: drug effects (MeSH) ; Adult (MeSH) ; Retrospective Studies (MeSH) ; Adolescent (MeSH) ; Middle Aged (MeSH) ; Young Adult (MeSH) ; Antioxidants: therapeutic use (MeSH) ; Antioxidants: pharmacology (MeSH) ; Disease Progression (MeSH) ; DNA, Mitochondrial: genetics (MeSH) ; Disease progression ; Leber hereditary optic neuropathy ; Mitochondrial disease ; Natural history ; Optic neuropathy ; idebenone ; Ubiquinone ; Antioxidants ; DNA, Mitochondrial

Classification:

Contributing Institute(s):
  1. Clinical Research (Munich) (Clinical Research (Munich))
Research Program(s):
  1. 353 - Clinical and Health Care Research (POF4-353) (POF4-353)

Database coverage:
Medline ; BIOSIS Previews ; Biological Abstracts ; Clarivate Analytics Master Journal List ; Current Contents - Life Sciences ; DEAL Springer ; DEAL Springer ; Ebsco Academic Search ; Essential Science Indicators ; IF >= 5 ; JCR ; NationallizenzNationallizenz ; SCOPUS ; Science Citation Index Expanded ; Web of Science Core Collection
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 Record created 2026-10-30, last modified 2026-10-30


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