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OCTA Biomarker Search in Patients with nAMD: Influence of Retinal Fluid on Time-Dependent Biomarker Response

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CURRENT EYE RESEARCH
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TAYLOR & FRANCIS INC
DOI: 10.1080/02713683.2023.2184318

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Retina; nAMD; biomarker; SSOCTA; MNV

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This study aimed to evaluate the individual influence of retinal thickness, intra- and sub-retinal fluid on the treatment response in patients with neovascular AMD. The results showed that retinal thickness and the presence of intra- and sub-retinal fluid had an impact on the treatment response, while junction density and vessel density did not.
PurposePrevious studies have identified a link between optical coherence tomography (OCT)-derived and OCT angiography (OCTA)-based parameters in patients with neovascular AMD (nAMD); the latter may serve as direct biomarkers for macular neovascularization (MNV) activity. The aim of this study was to assess the individual influence of retinal thickness (RT) as well as intra- and sub-retinal fluid (IRF, SRF) presence on the treatment response over time as assessed by previously identified OCTA-derived MNV vascular parameters.MethodsDuring the first 3 months of anti-VEGF therapy patients were prospectively followed. RT, SRF and IRF were determined from SSOCT/A (PlexElite, Zeiss) images and using the semi-automated AngioTool software, vessel area (VA), total vessel length (TVL), total number of junctions (TNJ), junction density (JD), vessel density (VD) as well as MNV area were exported. IRF and SRF were identified manually on OCT volume scans .The associations between RT, IRF, and SRF and SSOCTA vascular parameters were analyzed using linear mixed models.Results31 eyes of 31 patients with treatment-naive and OCTA-positive nAMD MNV were included in this analysis. VA, TVL, TNJ, and MNV area show a statistically significant change over time in response to anti-VEGF treatment, even after correcting for the presence of SRF, IRF, or RT (all p < 0.05). This is not the case for JD and VD (both p > 0.05).ConclusionsOCTA-based parameters VA, TVL, TNJ, and MNVarea show a strong response to anti-VEGF therapy over time, independent of the presence of IRF, SRF or RT. We conclude that the above listed OCTA parameters could contribute to our understanding of MNV biology and to guide individualized treatment in the future.Trial registryThe authors confirm that all ongoing and related trials are registered. ClinicalTrials.gov Number: NCT02521142

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