AI-inspired texture analysis detects “silent” retinal damage in early diabetes
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AI-inspired texture analysis detects “silent” retinal damage in early diabetes

27/11/2025 TranSpread

Diabetic retinopathy (DR) is a leading cause of blindness among working-age adults, affecting more than 130 million people worldwide. Although advances in ophthalmic imaging have improved disease monitoring, most patients are diagnosed only after years of unrecognized retinal damage. Early molecular and cellular changes—including neurodegeneration, inflammation, and vascular dysfunction—often remain undetectable with standard methods such as fundus photography or angiography. As a result, patients may experience irreversible vision impairment before diagnosis. Due to these limitations, new noninvasive imaging biomarkers are urgently needed to detect subclinical retinal alterations at the earliest stages of diabetes.

A research team from the University of Coimbra, Portugal, has developed a texture-based analysis of optical coherence tomography (OCT) images capable of detecting early retinal changes in type 2 diabetes. The study, published (DOI: 10.1186/s40662-025-00451-3) in Eye and Vision on September 3, 2025, used a high-fat-diet and low-dose streptozotocin rat model to monitor retinal alterations over 12 weeks. By quantifying microscopic texture variations, the method revealed early neurovascular abnormalities that occurred well before traditional biomarkers or vascular leakage.

Using advanced image analysis, the researchers evaluated over 80 retinal scans from diabetic and control rats, applying a gray-level co-occurrence matrix (GLCM) approach to quantify texture parameters across retinal layers. Among the 20 features examined, eight—including autocorrelation, cluster prominence, correlation, homogeneity, information measure of correlation II (IMCII), inverse difference moment normalised (IDN), inverse difference normalised (INN), and sum average—showed significant changes in diabetic retinas, particularly in the inner plexiform layer (IPL) and photoreceptor segments (IS/OS). Interestingly, seven of these metrics had also been altered in a previous study using a type 1 diabetes model, reinforcing their diagnostic consistency. Despite minimal thinning and delayed oscillatory potentials, the retinas displayed no major inflammation or vascular leakage, confirming that texture changes precede overt pathology. The findings highlight texture analysis as a sensitive, quantitative method for detecting early structural disorganization in the retina—potentially bridging the gap between biological alterations and clinical diagnosis.

“Our results demonstrate that texture analysis can uncover minute retinal changes long before DR becomes clinically visible,” said Professor António Francisco Ambrósio, co-senior author of the study. “By capturing subtle structural signals within OCT images, this approach opens a new diagnostic window into the earliest disease processes. It offers a way to identify high-risk patients before permanent vision damage occurs, supporting earlier treatment and better outcomes. The coherence of these texture metrics across diabetes models strengthens their potential as universal early biomarkers.”

This research paves the way for developing AI-assisted diagnostic tools that automatically screen for preclinical DR based on retinal texture signatures. Integrating this analysis into routine OCT imaging could allow ophthalmologists to identify patients who show microscopic structural disruption—even when their vision appears normal. Such early detection may help tailor personalized care, prevent irreversible retinal damage, and reduce the global burden of diabetic blindness. Further clinical trials are now needed to validate these findings in human subjects and refine algorithms for large-scale screening and teleophthalmology applications.

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References

DOI

10.1186/s40662-025-00451-3

Original Source URL

https://doi.org/10.1186/s40662-025-00451-3

Funding Information

This study was supported by the Foundation for Science and Technology, Portugal: 2020.07432.BD, PEst UIDB/04539/Base/2020 and UIDP/04539/Programatico/2020, PEst UIDB/04950/Base/2020 and UIDP/04950/Programatico/2020 and PEst UIDB/04539/Base/2025 and UIDP/04539/Programático/2025. This study was also supported by the Sociedade Portuguesa de Diabetologia (SPD), Portugal: Bolsa Charneco da Costa—Investigação Fundamental em Diabetologia, Bolsas e Prémios SPD 2024.

About Eye and Vision

Eye and Vision is an open access, peer-reviewed journal for ophthalmologists and visual science specialists. It welcomes research articles, reviews, commentaries, case reports, perspectives and short reports encompassing all aspects of eye and vision. Topics of interest include but are not limited to: current developments of theoretical, experimental and clinical investigations in ophthalmology, optometry and vision science which focus on novel and high-impact findings on central issues pertaining to biology, pathophysiology and etiology of eye diseases as well as advances in diagnostic techniques, surgical treatment, instrument updates, the latest drug findings, results of clinical trials and research findings. It aims to provide ophthalmologists and visual science specialists with the latest developments in theoretical, experimental and clinical investigations in eye and vision.

Paper title: Early retinal changes in type 2 diabetes detected by texture-based OCT analysis: potential approach for subclinical diabetic retinopathy diagnosis
Fichiers joints
  • Diabetes triggers slight immunoreactive changes in tight junction proteins, without changes in retinal vascular permeability. Diabetic Wistar Han rats (induced by a 12-week HFD with STZ injection at week 4; 35 mg/kg, IP; T2D group) presented a slight decrease in claudin-5 immunoreactivity after 8 weeks on HFD, as well as in occludin and claudin-5 immunostaining at week 12, as assessed in retinal wholemounts. However, no differences were found in its protein levels in retinal extracts, assessed by Western blot, compared to age-matched controls (Control group). No vascular leakage was detected in diabetic animals, as assessed by the Evans blue assay. Representative images of retinal wholemounts immunostained for (a) claudin-5, (b) occludin, and (c) ZO-1. (d) Representative images showing Evans blue fluorescence in the retina. (e) Claudin-5, (f) occludin, and (g) ZO-1 protein levels assessed by Western blot, normalised to the loading control (calnexin), and expressed as percentage of the respective control. Representative images of protein immunoreactive bands are presented above the graphs, with the respective loading control (calnexin). Data are presented as mean ± SEM. Statistical analysis was performed using the Student’s t-test, or the Mann–Whitney test, if data were not normally distributed. HFD, high-fat diet; STZ, streptozotocin; IP, intraperitoneal; T2D, type 2 diabetes; ZO-1, zonula occludens-1.
27/11/2025 TranSpread
Regions: North America, United States, Europe, Portugal
Keywords: Health, Medical

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