Evidence map›Paper›PMID 42494389›Full record

ArticleFrontiers in ophthalmology2026

Longitudinal changes in anatomic biomarkers on optical coherence tomography angiography in diabetic retinopathy.

Rachel Liu, Isaac Bakis, Megan Steinkerchner, Kevin Sun, Sapna Gangaputra, Stephen J Kim, Lok Hin Lee

Abstract read
In one paragraph

Article in Frontiers in ophthalmology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Rachel LiuVanderbilt University School of Medicine, Nashville, TN, United States.
Isaac BakisVanderbilt University School of Medicine, Nashville, TN, United States.
Megan SteinkerchnerVanderbilt Eye Institute, Nashville, TN, United States.
Kevin SunVanderbilt University School of Medicine, Nashville, TN, United States.
Sapna GangaputraVanderbilt Eye Institute, Nashville, TN, United States.
Stephen J KimVanderbilt Eye Institute, Nashville, TN, United States.
Lok Hin LeeVanderbilt University School of Medicine, Nashville, TN, United States.

Funding

Ocular Inflammatory Mediators in the Pathophysiology of Diabetic RetinopathyR01EY031315 · NEI · VANDERBILT UNIVERSITY MEDICAL CENTER · PI KIM, STEPHEN JAE · 2020 to 2024
$2.1M
NEI NIH HHS R01 EY031315
6 · The paper itself

Abstract

Purpose: To identify optical coherence tomography angiography (OCTA)-derived biomarkers correlating with diabetic retinopathy (DR) severity and characterize longitudinal retinal microvascular changes across DR stages. Methods: In this 3-year prospective study, we analyzed OCTA images from 328 eyes of 164 adults with type II diabetes and 33 eyes from 17 healthy controls. Patients were categorized as no DR, mild, moderate, or severe nonproliferative DR (NPDR), or proliferative DR (PDR) at baseline. Bilateral OCTA scans were obtained at each visit and processed with a validated pipeline to extract seven microvascular indices from the superficial and deep capillary plexuses: vessel density, skeleton density, acircularity index, average vessel caliber, foveal avascular zone (FAZ) area, FAZ perimeter, and fractal dimensions. Linear regression quantified changes over time, and intergroup comparisons were made using ANOVA and Results: A total of 361 eyes (328 diabetic eyes and 33 control eyes) were followed for a mean of 3 years. Longitudinal analysis demonstrated stage-dependent microvascular changes across DR severity groups. In the deep capillary plexus, eyes with severe NPDR exhibited greater annual declines in vessel density (-0.563 ± 0.39% per year) and skeleton density (-0.296 ± 0.23% per year) compared with controls. Acircularity index increased over time, with greater annual increases observed in severe NPDR relative to mild NPDR (0.16 ± 0.12% per year), consistent with progressive macular ischemia. In the superficial plexus, eyes with severe NPDR showed greater annual reductions in average vessel caliber (-4.5e-4 ± 0.0005% per year) compared with earlier disease stages. Across the cohort, most OCTA metrics demonstrated small but statistically significant longitudinal trends, reflecting gradual microvascular remodeling detectable over repeated measurements. Conclusions: Longitudinal OCTA analysis reveals stage-specific microvascular changes in DR. These dynamic biomarkers may provide early indicators of DR progression and offer a quantitative foundation for individualized monitoring and timely intervention strategies. Translational Relevance: OCTA-derived biomarkers offer a noninvasive tool for detecting early DR changes and guiding personalized care strategies.

Indexed as

biomarkerdiabetic retinopathynonproliferative diabetic retinopathyOCTAproliferative diabetic retinopathy

Identifiers

PMID42494389
PMCPMC13391325

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.