Abstract
Purpose
We sought to investigate the clinical features of eyes with unilateral type 3 macular neovascularization (MNV) according to the degenerative features of fellow eyes.
Methods
We retrospectively reviewed 55 patients with unilateral type 3 MNV and identified degenerative features including geographic atrophy (GA) in fellow eyes using multimodal imaging. Then, the clinical features of eyes with type 3 MNV at baseline and during follow-up with anti-vascular endothelial growth factor treatment and an as-needed regimen were compared according to the degenerative features of fellow eyes.
Results
Eighteen patients (32.7%) had GA in fellow eyes; initial disease manifestations of type 3 MNV eyes including stage, best-corrected visual acuity, and choroidal thickness (CT) did not vary between groups (all P > 0.05). During follow-up, a rate of complete fluid resolution after three monthly loading injections was not associated with GA in fellow eyes (P = 0.703), while a lower rate of early recurrence within 3 months after loading treatment was associated with thinner CT in type 3 MNV eyes and GA over one disc area in fellow eyes (P = 0.025 and P = 0.021).
Conclusion
Degenerative features of fellow eyes in patients with unilateral type 3 MNV may be associated with the clinical characteristics of affected eyes.
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Availability of data and materials
Data are available with the corresponding author on request.
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Funding
This work was supported by a grant from Korea University (K2212011).
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C.Y. conceived and designed this study. M.C., E.G.Y and K.T.N. contributed to the acquisition and interpretation of data. C.Y. and M.C analyzed the data and drafted the article. C.Y. prepared Fig. 1. All authors contributed to interpretation of results and were involved in critical revision and approval of the final version.
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Choi, M., Yoon, E.G., Nam, K.T. et al. Clinical features associated with the atrophy of fellow eyes in patients with unilateral type 3 macular neovascularization. Int Ophthalmol 43, 973–980 (2023). https://doi.org/10.1007/s10792-022-02499-9
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DOI: https://doi.org/10.1007/s10792-022-02499-9