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Author Spotlight: Overcoming Anti-VEGF Resistance Through Advanced Vascular Morphology Assessment in Choroidal Neovascularization
Published on: August 11, 2023
Choroidal neovascularization in eyes with choroidal vascular hyperpermeability
Masahiro Miyake1, Akitaka Tsujikawa2, Kenji Yamashiro2
1Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan Center for Genomic Medicine/Inserm U.852, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Choroidal vascular hyperpermeability (CVH) frequently involves type 1 choroidal neovascularization (CNV), sometimes with polypoidal lesions. Genetic factors in these patients differ from age-related macular degeneration (AMD) but resemble the general population.
Area of Science:
- Ophthalmology
- Medical Genetics
Background:
- Choroidal vascular hyperpermeability (CVH) is a condition affecting the choroid.
- Choroidal neovascularization (CNV) can occur in association with CVH.
Purpose of the Study:
- To investigate the clinical and genetic characteristics of choroidal neovascularization (CNV) in eyes with choroidal vascular hyperpermeability (CVH).
Main Methods:
- Cross-sectional study of 438 patients undergoing angiography for macular disease.
- Analysis of genotypes for ARMS2 and CFH in patients with CVH and CNV, compared to age-related macular degeneration (AMD) cases and general population controls.
Main Results:
- CVH was present in 26.1% of eyes, with 22.6% of those eyes showing CNV.
- Type 1 CNV was predominant (98%), with polypoidal lesions in 33.3% of type 1 CNV cases.
- Genetic analysis revealed significant differences in ARMS2 and CFH genotype distributions between patients with CVH and type 1 CNV and AMD cases, but similarity to the general population.
Conclusions:
- Type 1 CNV is common in patients with CVH and can be associated with polypoidal lesions.
- The genetic background of patients with CVH and type 1 CNV differs from AMD patients, aligning more closely with the general population.
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