Abstract
Abstract
Background
Voretigene neparvovec (Luxturna®) is the first approved gene therapy for RPE65-linked Leber congenital amaurosis (LCA). Though individual effects are highly variable, most recipients report improved vision in everyday life. To describe such effects, visual navigation tests are now frequently used in clinical trials. However, it is still unclear how their results should be interpreted compared to conventional parameters of visual function.
Methods
Seven LCA patients underwent a multi-luminance visual navigation test (Ora-VNCTM) before and 3 months after receiving Luxturna gene therapy. Their performance was rated based on the luminance level at which they passed the course. Differences between the first and second test were correlated to changes in visual acuity, full-field stimulus thresholds, chromatic pupil campimetry, and dark-adapted perimetry.
Results
A few patients displayed notable improvements in conventional measures of visual function whereas patients with advanced retinal degeneration showed no relevant changes. Independent of these results, almost all participants improved in the visual navigation task by one or more levels. The improvement in the mobility test was best correlated to the change in full-field stimulus thresholds. Other measures of visual functions showed no clear correlation with visual navigation.
Discussion
In patients who passed the test’s more difficult levels, improved visual navigation can be attributed to the reactivation of rods. However, the performance of patients with low vision seemed to depend much more on confounding factors in the easier levels. In sum, such tests might only be meaningful for patients with better preserved visual functions.
Funder
Universitätsklinikum Tübingen
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference14 articles.
1. Chao DL, Burr A, Pennesi M (1993) GeneReviews®. RPE65-related Leber congenital amaurosis/early-onset severe retinal dystrophy. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Mirzaa G, Amemiya A (eds) Seattle (WA)
2. Chung DC, McCague S, Yu Z-F, Thill S, DiStefano-Pappas J, Bennett J et al (2018) Novel mobility test to assess functional vision in patients with inherited retinal dystrophies. Clin Exp Ophthalmol 46(3):247–259. https://doi.org/10.1111/ceo.13022
3. Cideciyan AV, Jacobson SG, Drack AV, Ho AC, Charng J, Garafalo AV et al (2019) Effect of an intravitreal antisense oligonucleotide on vision in Leber congenital amaurosis due to a photoreceptor cilium defect. Nat Med 25(2):225–228. https://doi.org/10.1038/s41591-018-0295-0
4. den Hollander AI, Roepman R, Koenekoop RK, Cremers FPM (2008) Leber congenital amaurosis. Genes, proteins and disease mechanisms. Prog Retin Eye Res 27(4):391–419. https://doi.org/10.1016/j.preteyeres.2008.05.003
5. Jacobson SG, Aleman TS, Cideciyan AV, Sumaroka A, Schwartz SB, Windsor EAM et al (2005) Identifying photoreceptors in blind eyes caused by RPE65 mutations. Prerequisite for human gene therapy success. Proc Natl Acad Sci USA 102(17):6177–6182. https://doi.org/10.1073/pnas.0500646102
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