# Ultrasound-Enhanced Assessment of Vitreous Status in Exudative AMD: Associations with Neovascular Phenotypes, Treatment Burden, and Functional Outcomes

**Authors:** Cristina Rodriguez-Vidal, Lucía Galletero Pandelo, Nerea Martínez-Alday, Manuel Bande, María José Blanco Teijeiro

PMC · DOI: 10.3390/jcm15010167 · Journal of Clinical Medicine · 2025-12-25

## TL;DR

This study shows that ultrasound can reveal how vitreous detachment affects neovascular AMD, influencing treatment outcomes and visual improvement.

## Contribution

The study introduces ultrasound as a novel tool to assess vitreous status in nAMD, linking it to neovascular phenotypes and treatment response.

## Key findings

- Absence of posterior vitreous detachment (PVD) is more common in nAMD eyes and correlates with MNV type 2 lesions.
- Eyes without PVD showed greater visual improvement after anti-VEGF therapy compared to those with complete PVD.
- Complete PVD was associated with a higher treatment burden and similar intraretinal fluid changes across groups.

## Abstract

Background/Objectives: The influence of the vitreoretinal interface on neovascular age-related macular degeneration (nAMD) remains poorly characterized. Most previous studies relied solely on macular optical coherence tomography (OCT), which provides limited information about global posterior vitreous detachment (PVD). This study evaluated (1) whether ultrasonography-defined PVD status differs between nAMD eyes and healthy controls, and (2) whether baseline PVD influences macular neovascularization (MNV) phenotype and functional outcomes following anti-vascular endothelial growth factor (anti-VEGF) therapy. Methods: In this prospective longitudinal study, treatment-naïve nAMD eyes and population-based healthy controls underwent dynamic B-scan ultrasonography and spectral-domain OCT. PVD was categorized as absent, partial, or complete. nAMD eyes received intravitreal aflibercept according to a treat-and-extend protocol and were followed for 12 months. Structural parameters—including subretinal fluid (SRF), intraretinal fluid (IRF), and central foveal thickness—along with best-corrected visual acuity (BCVA) were recorded. A multivariable linear regression model was performed to assess whether PVD independently predicted BCVA gain after adjusting for age, baseline BCVA, MNV subtype, SRF, atrophy, and number of injections. Results: Absence of PVD was significantly more frequent in nAMD eyes than in controls (p < 0.001), whereas complete PVD prevalence was comparable. In nAMD, absence of PVD was associated with a higher prevalence of MNV type 2 (p = 0.032), while partial/complete PVD correlated with type 1 lesions. After 12 months, eyes without PVD achieved the greatest visual improvement (mean BCVA gain +0.34 ± 0.26), outperforming eyes with complete PVD (p = 0.026). A multivariable model confirmed that absence of PVD was an independent predictor of greater BCVA gain (β = −0.27; 95% CI −0.42 to −0.12; p = 0.0008). Eyes with complete PVD required more injections (p = 0.046). SRF and foveal-thickness reductions occurred across groups, whereas IRF changes were similar. Conclusions: Ultrasonography-defined PVD status differs markedly between nAMD and healthy eyes and independently influences neovascular phenotype and functional response to anti-VEGF therapy. These findings underscore the physiological importance of the vitreoretinal interface and support the use of ocular ultrasonography as an adjunct tool for assessing global vitreous status in selected nAMD settings.

## Linked entities

- **Diseases:** age-related macular degeneration (MONDO:0005150), AMD (MONDO:0005150)

## Full-text entities

- **Genes:** VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}
- **Diseases:** MNV type 2 (MESH:D057826), AMD (MESH:D006009), PVD (MESH:D020255), Neovascular (MESH:D016510), atrophy (MESH:D001284), age-related macular degeneration (MESH:D008268)

## Full text

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## Figures

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## References

58 references — full list in the complete paper: https://tomesphere.com/paper/PMC12787266/full.md

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Source: https://tomesphere.com/paper/PMC12787266