Investigative Ophthalmology & Visual Science Cover Image for Volume 65, Issue 7
June 2024
Volume 65, Issue 7
Open Access
ARVO Annual Meeting Abstract  |   June 2024
Widefield OCT Angiography Biomarkers for Predicting Clinically Significant Outcomes in Eyes with Nonproliferative Diabetic Retinopathy
Author Affiliations & Notes
  • Xinyi Ding
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Francesco Romano
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Itika Garg
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Jenny Gan
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Katherine Overbey Millner
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Mauricio De Jesus Garcia
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Filippos Vingopoulos
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Cade Frederick Bennett
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Jocelyn Rodriguez
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Matthew Finn
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Peyman Razavi
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Demetrios G. Vavvas
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Deeba Husain
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Nimesh Arvind Patel
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Joan W Miller
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • John B Miller
    Retina, Massachusetts Eye and Ear Department of Ophthalmology, Boston, Massachusetts, United States
  • Footnotes
    Commercial Relationships   Xinyi Ding None; Francesco Romano None; Itika Garg None; Jenny Gan None; Katherine Millner None; Mauricio Garcia None; Filippos Vingopoulos None; Cade Bennett None; Jocelyn Rodriguez None; Matthew Finn None; Peyman Razavi None; Demetrios Vavvas Olix Pharma, Valitor, TwentyTwenty, Sumitomo/Sunovion, Cambridge Polymer Group, , Code C (Consultant/Contractor), National Eye Institute, NIH, Research to Prevent Blindness, Loefflers Family Foundation, Yeatts Family Foundation, and Alcon Research Institute, Code F (Financial Support), Drusolv Therapeutics, Code O (Owner); Deeba Husain Allergan, Novartis, Genetech, Omeicos Therapeutics, Code C (Consultant/Contractor), NIH, National Eye Institute, Lions Vision Gift, Commonwealth Grant, Lions International, Syneos LLC, and the Macular Society, Code F (Financial Support); Nimesh Patel Alimera Sciences, Alcon, Allergan, Genentech, Eyepoint, Lifesciences Guidepoint, and GLG, Code C (Consultant/Contractor); Joan Miller Genentech/ Roche, Sunovion, KalVista Pharmaceuticals, ONL Therapeutics, Heidelberg Engineering, Code C (Consultant/Contractor), Lowy Medical Research Institute, National Eye Institute, Heidelberg Engineering, Code F (Financial Support), Ciendias Bio, Code I (Personal Financial Interest), Drusolv Therapeutics, ONL Therapeutics, Code P (Patent), Aptinyx, Inc., Sunovion, KalVista Pharmaceuticals, ONL Therapeutics,Valeant Pharmaceuticals/Mass. Eye and Ear, Code R (Recipient), Aptinyx, Inc., ONL Therapeutics, Code S (non-remunerative); John Miller Alcon, Allergan, Carl Zeiss, Sunovion, Genentech and Topcon, Code C (Consultant/Contractor)
  • Footnotes
    Support  None
Investigative Ophthalmology & Visual Science June 2024, Vol.65, 4873. doi:
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      Xinyi Ding, Francesco Romano, Itika Garg, Jenny Gan, Katherine Overbey Millner, Mauricio De Jesus Garcia, Filippos Vingopoulos, Cade Frederick Bennett, Jocelyn Rodriguez, Matthew Finn, Peyman Razavi, Demetrios G. Vavvas, Deeba Husain, Nimesh Arvind Patel, Joan W Miller, John B Miller; Widefield OCT Angiography Biomarkers for Predicting Clinically Significant Outcomes in Eyes with Nonproliferative Diabetic Retinopathy. Invest. Ophthalmol. Vis. Sci. 2024;65(7):4873.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose : To assess the utility of widefield swept-source optical coherence tomography angiography (WF SS-OCTA) imaging biomarkers in predicting the occurrence of clinically significant outcomes in eyes with nonproliferative diabetic retinopathy (NPDR).

Methods : Prospective longitudinal study. Participants with mild to severe NPDR with at least two WF SS-OCTA scans in consecutive visits over a follow-up period of at least 6 months were included. The presence of intraretinal microvascular abnormalities (IRMAs) at baseline and the stability of IRMAs during follow-up period on 12x12-mm angiography were evaluated. Stable IRMAs were defined as all IRMA lesions within the field of view that maintained their original structure, along with the surrounding non-perfused tissue. Baseline nonperfusion ischemia index (ISI) and other OCTA metrics were calculated on FIJI and ARI Network. Significant clinical outcomes were defined as one or more of the following: 1) 2-step or more DR progression (according to international clinical DR severity scale); 2) new development of center-involving diabetic macular edema; and 3) initiation of treatment with pan-retinal photocoagulation (PRP) or anti-VEGF injections during follow-up period. Cox mixed-effects regression models was used to explore the predictors for significant clinical outcomes.

Results : We included 88 eyes from 57 participants (age: 59.3±12.4). Over 28.6±10.5 months, 19.1% (17/88) eyes developed significant clinical outcomes. Univariate Cox mixed-effects regression analysis revealed that a higher baseline ISI and non-stable IRMAs during follow-up period were associated with the occurrence of significant clinical outcomes. In multivariable Cox mixed-effects regression models, a higher baseline ISI (hazard ratio: 1.10, p<0.001) and the lack of stability in IRMAs (hazard ratio: 0.19, p=0.002) remained significantly associated after adjusting for age, diabetes duration, and prior anti-VEGF injections at baseline.

Conclusions : In conclusion, NPDR eyes with worse retinal perfusion at baseline and non-stable IRMAs over time are in higher risk of developing significant clinical outcomes in the short term. Our findings suggest that WF-OCTA may offer additional prognostic benefits for clinical DR staging and predicting high-risk patients.

This abstract was presented at the 2024 ARVO Annual Meeting, held in Seattle, WA, May 5-9, 2024.

 

Figure 1. 12x12-mm OCTA angiography demonstrating stable IRMAs from baseline to follow-up.

Figure 1. 12x12-mm OCTA angiography demonstrating stable IRMAs from baseline to follow-up.

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