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Foveal Microvascular Integrity Association With Anti-VEGF Treatment Response for Diabetic Macular Edema
Wei-Hsuan Huang1, Chi-Chun Lai1,2,3, Lan-Hsin Chuang1,2
1Department of Ophthalmology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Purpose:
To investigate the association between foveal microvascular integrity and anti-vascular endothelial growth factor (VEGF) treatment response for diabetic macular edema (DME).
Methods:
This retrospective study enrolled 58 eyes (from 45 patients) with DME. Treatment strategy was three to five monthly anti-VEGF injections followed by a PRN protocol. Treatment with an intravitreal corticosteroid would be considered for persistent DME after five consecutive anti-VEGF injections. Eyes achieving a treatment-free interval ≥ four months within two years were classified into the good clinical course group (group 1). Eyes with frequent recurrent edema (treatment-free interval < four months) or requiring an intravitreal corticosteroid within two years were classified into the suboptimal clinical course group (group 2). Foveal microvascular integrity was evaluated by two continuous variables, that is, vessel density (%) within a width of 300 µm around the foveal avascular zone (FD-300) on optical coherence tomography angiography (OCTA) and perifoveal leakage (area %) on fluorescein angiography (FA).
Results:
There were 37 eyes in group 1 and 21 eyes in group 2. FD-300 (odds ratio 0.733, 95% CI 0.620-0.867, P < 0.001) and perifoveal leakage (odds ratio 1.064, 95% CI 1.007-1.124, P = 0.027) were significantly associated with suboptimal clinical course. Area under curve (AUC) was 0.820 for FD-300 and 0.723 for perifoveal leakage in predicting clinical course. FD-300 was negatively correlated with perifoveal leakage (coefficient = -0.325, P = 0.014).
Conclusions:
Compromised foveal microvascular integrity, represented by lower FD-300 and more severe perifoveal fluorescein leakage, was associated with suboptimal clinical course in anti-VEGF treatment for DME. A negative correlation between FD-300 and perifoveal leakage existed.
Insights
Diabetic macular edema (DME) patients with poor foveal microvascular integrity, indicated by lower vessel density and increased leakage, show a worse response to anti-vascular endothelial growth factor (VEGF) therapy. This highlights microvascular health as a key factor in DME treatment outcomes.
Area of Science:
- Ophthalmology
- Medical Imaging
- Vascular Biology
Background:
- Diabetic macular edema (DME) is a leading cause of vision loss in diabetic patients.
- Anti-vascular endothelial growth factor (anti-VEGF) therapy is a primary treatment for DME, but treatment response varies.
- Foveal microvascular integrity may influence treatment outcomes in DME.
Purpose of the Study:
- To assess the association between foveal microvascular integrity and the clinical course of diabetic macular edema following anti-VEGF treatment.
- To determine if measures of microvascular integrity can predict treatment response in DME patients.
Main Methods:
- Retrospective analysis of 58 eyes with DME treated with anti-VEGF injections.
- Classification of eyes into good (treatment-free interval ≥ 4 months) or suboptimal (recurrent edema or corticosteroid use) clinical course groups.
- Evaluation of foveal microvascular integrity using optical coherence tomography angiography (OCTA) for vessel density (FD-300) and fluorescein angiography (FA) for perifoveal leakage.
Main Results:
- Lower foveal vessel density (FD-300) and increased perifoveal leakage were significantly associated with a suboptimal clinical course.
- FD-300 (AUC 0.820) and perifoveal leakage (AUC 0.723) demonstrated predictive value for clinical course.
- A negative correlation was observed between FD-300 and perifoveal leakage (P = 0.014).
Conclusions:
- Compromised foveal microvascular integrity is linked to poorer outcomes in anti-VEGF treated DME.
- OCTA-derived vessel density and FA-derived leakage are potential biomarkers for predicting DME treatment response.
- Microvascular health is a critical factor in the management of diabetic macular edema.
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