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Am J OphthalmolNovember 202213 citations

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

HumansOptic Atrophy, Hereditary, LeberRetrospective StudiesTomography, Optical CoherenceRetinal Ganglion CellsCohort StudiesBiomarkersUbiquinone

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).

TreatmentCohortRetrospective, interventional, noncomparative clinical cohort studyn=34 eyes from 17 participantsCh7

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%.

TreatmentCohortRetrospective, interventional, noncomparative clinical cohort studyn=34 eyes from 17 participantsCh7

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.

PrognosisCohortRetrospective, interventional, noncomparative clinical cohort studyn=34 eyes from 17 participantsCh5Ch7

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.

PrognosisCohortRetrospective, interventional, noncomparative clinical cohort studyn=34 eyes from 17 participantsCh5Ch7

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