Visual Outcomes and Optical Coherence Tomography Biomarkers of Vision Improvement in Patients With Leber Hereditary Optic Neuropathy Treated With Idebenone.
Borrelli Enrico, Berni Alessandro, Cascavilla Maria Lucia, Barresi Costanza, Battista Marco, Lari Giorgio, Reibaldi Michele, Bandello Francesco, Barboni Piero
AI Summary
This study found that in LHON patients treated with idebenone, thinner baseline macular GC-IPL on OCT predicted worse long-term visual outcomes, offering prognostic insights.
Abstract
Purpose
To assess the relationship of demographics, clinical characteristics and structural optical coherence tomography (OCT) findings to long-term visual outcomes in patients with Leber hereditary optic neuropathy (LHON) treated with idebenone.
Design
Retrospective, interventional, noncomparative clinical cohort study.
Methods
In this study, a total of 17 participants (34 eyes) with LHON treated with idebenone therapy within 1 year after disease onset and 2 years (24 months) of regular follow-ups were retrospectively enrolled. At baseline, structural OCT volume scans of the macula and optic nerve were reviewed to measure metrics reflecting neuronal loss (ie, macular ganglion cell and inner plexiform layer [GC-IPL] and peripapillary retinal nerve fiber layer [RNFL] thicknesses). Stepwise multiple regression analyses were computed to assess associations between final best-corrected visual acuity (BCVA) at 2 years and change in BCVA from baseline at 2 years as dependent variables with demographics, clinical characteristics, and OCT metrics at baseline (visit before the initiation of treatment).
Results
The BCVA was 1.6±0.8 logMAR (Snellen VA of ∼20/800) at baseline (visit before the initiation of treatment) and 1.0±0.7 logMAR (Snellen VA of 20/200) at the 2-year follow-up visit (P < .0001). Mean±SD change in BCVA from baseline at 2 years was -51.9%±35.9%. In multivariable analysis, the strongest associations with final BCVA were with baseline BCVA (P = .012), superior macular GC-IPL thickness (P = .044), superotemporal macular GC-IPL thickness (P = .010), and inferotemporal macular GC-IPL thickness (P = .015). Similarly, the strongest associations with delta BCVA were with superior macular GC-IPL thickness (P = .045), superotemporal macular GC-IPL thickness (P = .047), and inferotemporal macular GC-IPL thickness (P = .030).
Conclusion
We identified OCT biomarkers associated with long-term (ie, 2-year) visual outcomes in patients with LHON treated with idebenone therapy in the first year after disease onset. Thinning of the GC-IPL in the superior and temporal parafoveal regions was associated with worse long-term visual outcomes in these patients.
MeSH Terms
Shields Classification
Key Concepts4
In patients with Leber hereditary optic neuropathy (LHON) treated with idebenone within 1 year after disease onset, the best-corrected visual acuity (BCVA) improved from 1.6±0.8 logMAR (Snellen VA of ~20/800) at baseline to 1.0±0.7 logMAR (Snellen VA of 20/200) at the 2-year follow-up visit (P < .0001).
In patients with Leber hereditary optic neuropathy (LHON) treated with idebenone, the mean±SD change in best-corrected visual acuity (BCVA) from baseline at 2 years was -51.9%±35.9%.
In patients with Leber hereditary optic neuropathy (LHON) treated with idebenone, baseline best-corrected visual acuity (BCVA) (P = .012), superior macular ganglion cell and inner plexiform layer (GC-IPL) thickness (P = .044), superotemporal macular GC-IPL thickness (P = .010), and inferotemporal macular GC-IPL thickness (P = .015) were significantly associated with final BCVA at 2 years.
In patients with Leber hereditary optic neuropathy (LHON) treated with idebenone, superior macular ganglion cell and inner plexiform layer (GC-IPL) thickness (P = .045), superotemporal macular GC-IPL thickness (P = .047), and inferotemporal macular GC-IPL thickness (P = .030) were significantly associated with the change in best-corrected visual acuity (delta BCVA) at 2 years.
Related Articles5
Maraviroc Prevents Optic Nerve Injury-Induced Retinal Ganglion Cell Apoptosis by Modulating the CCL5/CCR5/CTSS Axis.
Basic ScienceThe Mechanisms of Neuroprotection by Topical Rho Kinase Inhibition in Experimental Mouse Glaucoma and Optic Neuropathy.
Basic ScienceTopical Application of Bunazosin Hydrochloride Suppresses Myopia Progression With an Increase in Choroidal Blood Perfusion.
Basic ScienceOral Intake of Hydrogen Water Improves Retinal Blood Flow Dysregulation in Response to Flicker Stimulation and Systemic Hyperoxia in Diabetic Mice.
Basic ScienceDose-Related Side Effects of Intravitreal Injections of Humanized Anti-Vascular Endothelial Growth Factor in Rats: Glial Cell Reactivity and Retinal Ganglion Cell Loss.
Basic ScienceIs this article assigned to the wrong chapter(s)? Let us know.