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Updated: Apr 29, 2026

Application of Optical Coherence Tomography to a Mouse Model of Retinopathy
Published on: January 12, 2022
Characterization of punctate inner choroidopathy using enhanced depth imaging optical coherence tomography
Javier Zarranz-Ventura1, Dawn A Sim2, Pearse A Keane3
1Medical Retina Service, Moorfields Eye Hospital NHS Foundation Trust, London, United Kingdom; NIHR Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, United Kingdom; Department of Ophthalmology, Clínica Universidad de Navarra, Pamplona, Navarra, Spain.
Enhanced depth imaging optical coherence tomography (EDI-OCT) revealed subclinical inflammation in punctate inner choroidopathy (PIC). Retinal thickness in PIC patients is linked to disease type and duration, suggesting EDI-OCT can assess inflammatory status.
Area of Science:
- Ophthalmology
- Medical Imaging
- Retinal Diseases
Background:
- Punctate inner choroidopathy (PIC) is an inflammatory condition affecting the retina and choroid.
- Enhanced depth imaging optical coherence tomography (EDI-OCT) provides high-resolution cross-sectional images of the posterior eye.
- Understanding the morphological changes in PIC is crucial for diagnosis and management.
Purpose of the Study:
- To qualitatively and quantitatively analyze retinal and choroidal morphology in patients with punctate inner choroidopathy (PIC) using enhanced depth imaging optical coherence tomography (EDI-OCT).
- To identify potential indicators of subclinical inflammation and disease activity.
Main Methods:
- A cross-sectional study of 35 eyes from 35 patients with clinically inactive PIC.
- Qualitative assessment of PIC lesions for retinal and choroidal features using EDI-OCT.
- Quantitative analysis of retinal and choroidal layer thickness.
- Examination of associations between morphology, clinical data, and demographic factors.
Main Results:
- Ninety PIC lesions showed focal atrophy (46.6%), sub-RPE hyperreflective deposits (34.4%), or RPE elevation with hyporeflective space (18.8%).
- Inner choroidal hyperreflective dots were present in 68.5% of patients; focal choroidal thinning was observed in 17.1%.
- In non-highly myopic eyes, atypical PIC had reduced retinal thickness compared to typical PIC (P=0.04), and longer disease duration correlated with decreased retinal thickness (P=0.01).
Conclusions:
- One-fifth of PIC lesions showed RPE elevation with a hyporeflective space, suggesting subclinical inflammation.
- Retinal thickness is associated with PIC disease type and duration in non-highly myopic eyes.
- EDI-OCT facilitates noninvasive assessment of inflammatory status in PIC.
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