Microaneurysm Turnover in Mild Non-Proliferative Diabetic Retinopathy is Associated with Progression and Development

Ana Rita Santos1,2,3,4, Luis Mendes1, Maria Helena Madeira1,3,4

  • 1AIBILI-Association for Innovation and Biomedical Research on Light and Image, 3000-548 Coimbra, Portugal.

Abstract

Insights

Microaneurysm turnover (MAT) predicts diabetic retinopathy (DR) progression and vision-threatening complications like diabetic macular edema (DME) and proliferative retinopathy (PDR) in type 2 diabetes (T2D) patients.

Area of Science:

  • Ophthalmology
  • Diabetology
  • Medical Imaging Analysis

Background:

  • Retinal microaneurysm turnover (MAT) aids in identifying eyes at risk for diabetic retinopathy (DR) complications.
  • Characterizing MAT further can enhance its role as a predictive biomarker for DR progression and vision-threatening outcomes.

Purpose of the Study:

  • To characterize microaneurysm turnover (MAT) as a predictive biomarker for diabetic retinopathy (DR) progression.
  • To assess MAT's ability to predict the development of vision-threatening complications in individuals with type 2 diabetes (T2D).

Main Methods:

  • A 5-year prospective longitudinal study involving 212 individuals with type 2 diabetes (T2D), ETDRS grades 20 and 35.
  • Annual evaluations using color fundus photography and optical coherence tomography.
  • Microaneurysm turnover (MAT) analysis (MA formation/disappearance rates) via RetMarkerDR®, with endpoints of diabetic macular edema (DME) or proliferative retinopathy (PDR).

Main Results:

  • MAT analysis at 1 year showed significant differences between groups developing endpoints (p=0.018), notably the MA disappearance rate (p=0.007).
  • MAT also demonstrated significant differences correlating with ETDRS severity progression over the 5-year study period (p=0.035).

Conclusions:

  • Microaneurysm turnover (MAT) serves as an indicator for the development of diabetic macular edema (DME) and/or proliferative retinopathy (PDR).
  • MAT also predicts the progression of diabetic retinopathy (DR) severity in individuals with type 2 diabetes (T2D) and mild retinopathy.

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