Predicting the Risk of Diabetic Neurodegenerative Disorders by Artificial Intelligence Tools Based on Retinal Imaging

NCT06541834 | Recruiting

• 1 other identifier: DINEURET
• Study Type: observational
• Target: 250
• Locations: 1 country
• Sites: 1

Brief Summary

Diabetic Retinopathy (DR) is the most frequent complication of diabetes, and its presence and severity are related to the appearance of both micro and macrovascular events. Risk profiles have been suggested as a major direction for research in diabetes, based on non- invasive retinal imaging evaluations. There has been promising evidence that artificial intelligence (AI) based on fundus photographs can detect clinical metrics and systemic conditions invisible to expert human observers. Notably, deep-learning (DL) convolutional neural networks (CNNs) developed for retinal photographs have been shown superior performance in the detection of DR compared with human assessment. The relationship between retinal vascular abnormalities and neurovascular complications of diabetes has been reported. The retina is a window to the body that allows a non-invasive observation of microvascular and neural tissues. However, in clinical practice there are no reported phenotypic indicators or reliable examinations to identify type 2 diabetic (T2D) patients with neurodegenerative/cognitive impairment. The presence of cognitive Impairment is a very frequent complication in diabetic patients, reported up to 60% of the diabetics when compared to only 11 % in the non-diabetics (OR of 8.78). Furthermore, AI based on retinal imaging has never been applied before to predict the onset and worsening of neurodegenerative/cognitive impairment of T2D in a real-world setting. The aim of this project is to develop trustworthy AI tools for predicting the risk of developing and progressing of neurodegenerative/cognitive diabetic impairment based on retinal images, in T2D population. For the development and validation of these tools, T2D patients will be enrolled from 4 well-established Italian centers. The proposal of this study is addressed to health care systems, in order to improve their consciousness about diabetic neurodegenerative/cognitive complications and reduce the related economic burden. Since the huge majority of these disorders remain undiagnosed, DINEURET will provide new cost-effective screening strategies to identify these patients. 4 centers will be involved:

• 75 patients will be included in the IRCCS Ospedale San Raffaele, Milan;
• 75 patients will be included in the IRCCS MultiMedica, Milan;
• 50 patients will be included in the Ospedale Della Murgia "Fabio Perinei", Altamura;
• 50 patients will be included in the Azienda Ospedaliero-Universitaria (AOUI) of Cagliari, Cagliari.

Conditions

Diabete Mellitus; Cognitive Impairment

Outcome Measures

Primary Outcomes (1)

• Accuracy of AI based model

  To evaluate the accuracy (sensibility and specificity) of the AI based model in the prediction of a worsening of neurodegenerative/cognitive impairment (defined as \> 2 point decrease at Montreal Cognitive Assessment scale) based on the retinal imaging acquired at the baseline.

  30 August 2026

Secondary Outcomes (2)

• Reliability and reproducibility of the AI based model To characterize clinical phenotypes within T2D based on the risk of developing and worsening of cognitive decline.

  30 August 2026

• Clinical phenotypes of T2D patients

  30 August 2026

Interventions

Retinal imaging DEVICE

Data of retinal imaging were acquired using Spectralis (Heidelberg, Germany) and California (Optos, UK).

Eligibility Criteria

• Age: 45 Years+
• Sex: all
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Male or female \>45 years old affected by type 2 diabetes.

You may qualify if:

• Male or female \> 45 years-old;
• Diagnosis of type 2 DM;
• No previous treatment for diabetic retinopathy;
• Clear ocular media;
• Ability to communicate well with the Investigator and to understand and comply with the requirements of the study;
• Ability to provide written informed consent in accordance with institutional, local and national regulatory guidelines and to attend all study visits

You may not qualify if:

• Patients affected by other retinal disease than diabetic retinopathy;
• Presence of diabetic macular edema;
• Presence of proliferative diabetic retinopathy;
• Any media opacities, including corneal opacity, cataract formation and hemorrhage in the vitreous body, which may interfere with viewing by the laser surgeon of the target structures in the study eye(s). Subject requiring cataract surgery in the next 12 months must be excluded;
• Aphakic eye(s) with vitreous in the anterior chamber;
• Neovascular glaucoma;
• Glaucoma caused by congenital angle anomalies;
• Open angle of less than 90º or extensive peripheral anterior and low synechia, present circumferentially around the corner;
• Glaucoma secondary to active uveitis;
• Any other ocular condition that would progress in the study period and confound visual acuity assessment a part from diabetic retinopathy;
• Presence of idiopathic or autoimmune-associated uveitis;
• Any ocular or systemic medication known to be toxic to the lens, retina or optic nerve;
• Any intra-ocular surgery on a qualifying eye within three months prior to entry in the study;
• Any prior thermal laser in the macula or intravitreal injections or panphotocoagulation;
• History of vitrectomy, filtering surgery, corneal transplant or retinal detachment surgery;

Sponsors & Collaborators

• Ospedale San Raffaele: lead
• Riccardo Sacconi: collaborator
• Ilaria Zucchiatti: collaborator

Study Sites (1)

Ospedale San Raffaele

Milan, 20138, Italy

RECRUITING

MeSH Terms

Conditions

Diabetes Mellitus; Cognitive Dysfunction

Condition Hierarchy (Ancestors)

Glucose Metabolism Disorders; Metabolic Diseases; Nutritional and Metabolic Diseases; Endocrine System Diseases; Cognition Disorders; Neurocognitive Disorders; Mental Disorders

Central Study Contacts

Giuseppe Querques, MD, PhD

CONTACT

00390226432648; giuseppe.querques@hotmail.com

Riccardo Sacconi, MD, PhD

CONTACT

ric.sacconi@gmail.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: MD, PhD

Study Record Dates

• First Submitted: July 26, 2024
• First Posted: August 7, 2024
• Study Start: August 30, 2024
• Primary Completion: April 1, 2026
• Study Completion (Estimated): August 30, 2026
• Last Updated: March 14, 2025

Record last verified: 2025-03

Locations

IT (1)