Choriocapillaris and choroidal thickness in all Leber hereditary optic neuropathy stages using swept source technology

Author:

Castillo Lorena1ORCID,Berrozpe‐Villabona Clara234,Miserachs‐García Sergio5ORCID,Haulani Hanan1,Gómez‐Gutiérrez Cecilia1,González‐Martínez Alba1,Morilla‐Grasa Antonio1,Arias Luis67,Caminal José M.67,Casaroli‐Marano Ricardo8

Affiliation:

1. Institut Català de Retina (ICR) Barcelona Spain

2. Department of Ophthalmology Clínica Universidad de Navarra Madrid Spain

3. Department of Ophthalmology Clínica Universidad de Navarra Pamplona Spain

4. Thematic Network of Cooperative Health Research in Eye Diseases (Oftared) Health Institute Carlos III Madrid Spain

5. Institut Clínic d'Oftalmologia (ICOF) – Seu Plató Hospital Clínic de Barcelona Barcelona Spain

6. Department of Ophthalmology Bellvitge University Hospital, L'Hospitalet de Llobregat Barcelona Spain

7. Bellvitge Biomedical Research Institute (IDIBELL) L'Hospitalet de Llobregat Barcelona Spain

8. Department of Surgery, School of Medicine and Health Sciences Hospital Clínic de Barcelona, Universitat de Barcelona Barcelona Spain

Abstract

AbstractPurposeThe role of the choroid in Leber hereditary optic neuropathy (LHON) remains unclear. The literature is scarce, with conflicting results and lacks axial length measurements. Therefore, we aimed to analyse the choriocapillaris (CC) vessel density (VD) and choroidal thickness (ChT) in all stages of LHON using swept source (SS) technology and considering the possible influence of axial length on choroidal parameters.MethodsThis was a prospective cross‐sectional observational study. A total of 119 eyes of 60 patients with molecularly confirmed LHON across all stages and 120 eyes of 60 control participants were included. We obtained the CC VD using optical coherence tomography angiography maps centred on the fovea. ChT was measured from the Bruch's membrane to the choroid‐sclera interface in the macular and peripapillary regions.ResultsThe CC VD was not significantly affected in any sector or average, except for a slight change in the superior region of chronic eyes (52.08 ± 1.62% vs. 53.50 ± 2.29%, p = 0.002). ChT demonstrated a trend towards decreased values in asymptomatic eyes and increased values in the symptomatic stages that failed to reach statistical significance in sectors corresponding to the papillomacular bundle except for the macular nasal inner sector of chronic eyes (281.10 ± 67.12 μm vs. 252.08 ± 70.55 μm, p = 0.045). No significant correlations were observed between visual acuity and CC VD or ChT.ConclusionThe CC VD remained stable across the LHON stages. Choroidal vasculature does not appear to play a role in LHON pathophysiology. Further research is needed on ChT as a potential biomarker of LHON.

Publisher

Wiley

Subject

Ophthalmology,General Medicine

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