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Peer-reviewedCC BY-NC 4.0European Journal of Ophthalmology

Distinct interactions between macular neovascularization and geographic atrophy: Growth dynamics and fellow-eye risk

  1. 1Department of Ophthalmology, University of Pittsburgh, School of Medicine, Pittsburgh, PA, US
  2. 2Eye Clinic, Department of Experimental and Clinical Medicine, Polytechnic University of Marche, 60126 Ancona, Italy
  3. 3Shiraz University of Medical Science, School of Medicine, Shiraz, Fars, Iran

Abstract

Purpose: To compare geographic atrophy (GA) growth in eyes with and without macular neovascularization (MNV) and evaluate anti-VEGF therapy effects on GA progression.

Methods: One eye per patient with GA with one-year of follow-up was included. Patients who developed MNV in previously diagnosed GA were assigned to the MNV-GA group, while those who did not were assigned to the non-MNV group. OCT determined MNV location and type. GA was quantified from RPE en-face images using ImageJ over one year. Fellow eyes were followed to last visit. Analyses used SPSS with Mann–Whitney U; P < 0.05 denoted significance, and prespecified thresholds applied throughout analyses.

Results: A total of 60 eyes from 60 patients were included (mean age: 82.75 ± 7.31; 56.7% female). A significant difference in GA area growth over one year was observed between two groups, with slower GA enlargement in MNV-GA group (1.15 mm2 vs. 2.36 mm2; P = 0.001; and square root: 0.38 ± 0.28 vs. 0.46 ± 0.36; P = 0.040). In MNV-GA eyes, GA growth showed no correlation with the number of anti-VEGF injections (P = 0.692). Most MNVs were type 1 (46.7%) and type 2 (43.3%) and were predominantly located at the GA border (70.0%), particularly in the central (30.0%) and superior (30.0%) sectors. Among the 60 fellow-eyes, 27 (45.0%) developed MNV during follow-up. Of these, 25 eyes (83.3%) were from patients from MNV-GA group, whereas only 2 eyes (6.7%) were from non-MNV group (P < 0.001).

Conclusion: Eyes with MNV-GA showed slower GA enlargement over one-year, regardless of anti-VEGF frequency, and higher fellow-eye MNV risk, indicating shared risk factors but distinct mechanisms influencing disease progression.

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BibTeX
@article{sadeghi2026distinct,
  title = {{Distinct interactions between macular neovascularization and geographic atrophy: Growth dynamics and fellow-eye risk}},
  author = {Elham Sadeghi and Giulia Gregori and Joseph DeCicco and Zahra Sadeghi and Priyanka Gandhi and Sandeep Chandra Bollepalli and Kiran Kumar Vupparaboina and Jose Alain Sahel and Andrew W Eller and Jay Chhablani},
  journal = {European Journal of Ophthalmology},
  year = {2026},
  month = jul,
  doi = {10.1177/11206721261461910},
  url = {https://doi.org/10.1177/11206721261461910},
  note = {CC BY-NC 4.0},
}
RIS
TY  - JOUR
TI  - Distinct interactions between macular neovascularization and geographic atrophy: Growth dynamics and fellow-eye risk
AU  - Elham Sadeghi
AU  - Giulia Gregori
AU  - Joseph DeCicco
AU  - Zahra Sadeghi
AU  - Priyanka Gandhi
AU  - Sandeep Chandra Bollepalli
AU  - Kiran Kumar Vupparaboina
AU  - Jose Alain Sahel
AU  - Andrew W Eller
AU  - Jay Chhablani
PY  - 2026
DA  - 2026/07/06
JO  - European Journal of Ophthalmology
DO  - 10.1177/11206721261461910
UR  - https://doi.org/10.1177/11206721261461910
AB  - Purpose: To compare geographic atrophy (GA) growth in eyes with and without macular neovascularization (MNV) and evaluate anti-VEGF therapy effects on GA progression.  Methods: One eye per patient with GA with one-year of follow-up was included. Patients who developed MNV in previously diagnosed GA were assigned to the MNV-GA group, while those who did not were assigned to the non-MNV group. OCT determined MNV location and type. GA was quantified from RPE en-face images using ImageJ over one year. Fellow eyes were followed to last visit. Analyses used SPSS with Mann–Whitney U; P < 0.05 denoted significance, and prespecified thresholds applied throughout analyses.  Results: A total of 60 eyes from 60 patients were included (mean age: 82.75 ± 7.31; 56.7% female). A significant difference in GA area growth over one year was observed between two groups, with slower GA enlargement in MNV-GA group (1.15 mm2 vs. 2.36 mm2; P = 0.001; and square root: 0.38 ± 0.28 vs. 0.46 ± 0.36; P = 0.040). In MNV-GA eyes, GA growth showed no correlation with the number of anti-VEGF injections (P = 0.692). Most MNVs were type 1 (46.7%) and type 2 (43.3%) and were predominantly located at the GA border (70.0%), particularly in the central (30.0%) and superior (30.0%) sectors. Among the 60 fellow-eyes, 27 (45.0%) developed MNV during follow-up. Of these, 25 eyes (83.3%) were from patients from MNV-GA group, whereas only 2 eyes (6.7%) were from non-MNV group (P < 0.001).  Conclusion: Eyes with MNV-GA showed slower GA enlargement over one-year, regardless of anti-VEGF frequency, and higher fellow-eye MNV risk, indicating shared risk factors but distinct mechanisms influencing disease progression.
SN  - 1120-6721
SN  - 1724-6016
ER  -