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. 2023 Sep 14;47(5-6):237-247.
doi: 10.1080/01658107.2023.2251575. eCollection 2023.

Idebenone Treatment in Patients with OPA1-Dominant Optic Atrophy: A Prospective Phase 2 Trial

Affiliations

Idebenone Treatment in Patients with OPA1-Dominant Optic Atrophy: A Prospective Phase 2 Trial

Katharina Valentin et al. Neuroophthalmology. .

Abstract

The aim of this study was to evaluate the therapeutic effect of idebenone in patients with OPA1-dominant optic atrophy (DOA). Sixteen patients with genetically confirmed OPA1-DOA were treated with 900 mg idebenone daily for 12 months. The primary endpoint was the best recovery/least deterioration of visual acuity. Secondary endpoints were the changes of visual acuity, colour vision, contrast sensitivity, visual field, peripapillary retinal nerve fibre layer thickness (pRNFLT), and visual-related quality of life. For the primary endpoint, a significant increase was observed for the right eye (p = .0027), for the left eye (p = .0111) and for the better-seeing eye (p = .0152). For visual fields, a significant improvement was observed for the left eye between baseline and 9 months (p = .0038). Regarding pRNFLT, a significant decrease was found for the left eye between baseline and 3 months (p = .0413) and between baseline and 6 months (p = .0448). In the visual function questionnaire, a significant improvement was observed in the subscale general vision (p = .0156) and in the composite score (p = .0256). In conclusion, best recovery of visual acuity improved, even though the amount of improvement was small. Furthermore, a maintenance of visual function after 12 months of idebenone intake could be observed as well as a significant improvement in vision-related quality of life.Whether this effect is due to idebenone treatment, the placebo effect, or is explainable by the natural progression of DOA, remains unclear. Trial registration: EU Clinical Trials Register, EudraCT Number: 2019-001493-28.

Keywords: Dominant optic atrophy; OPA1; idebenone; optic neuropathy; visual function.

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Conflict of interest statement

K. Valentin received travel reimbursements from Chiesi Pharmaceuticals GmbH, H. Aminfar received travel reimbursements from Santhera Pharmaceuticals and Chiesi Pharmaceuticals GmbH. T. Klopstock received travel reimbursements and speaker honoraria from Santhera Pharmaceuticals and Chiesi Pharmaceuticals GmbH and M. Schneider received speaker honoraria from Santhera Pharmaceuticals. T. Georgi, R. Riedl, C. Singer, and A. Wedrich report no competing interests.

Figures

Figure 1.
Figure 1.
Box plots showing change of visual function within a 12-month period of idebenone treatment. (a) Best recovery or least deterioration of visual acuity. (b) Change of visual acuity. (c) Change of visual field. (d) Change of colour vision. (e) Change of contrast sensitivity. (f) Change of peripapillary retinal nerve fibre layer thickness. Solid lines represent median values and the symbols ‘o’, ‘+’ and ’ ×’ within the boxes represent mean values for OD (right eye), OS (left eye) and the better-seeing eye and ‘o’, ‘+’ and ’ ×’ outside depict outliers. logMAR = logarithm of the minimum angle of resolution; pRNFLT = peripapillary retinal nerve fibre layer thickness.

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