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Background: Artificial intelligence (AI)-driven analysis of retinal images holds promise for noninvasive, early detection of neurodegenerative disorders. We conducted a prospectively registered systematic review and meta‑analysis to quantify diagnostic accuracy of AI‑assisted retinal imaging across Alzheimer's disease (AD), Parkinson's disease (PD), and related conditions.
Methods: We searched six databases for studies (2010-2024) employing AI/ML models for binary classification of neurodegenerative disease versus healthy controls. Risk of bias was assessed using QUADAS-2. We extracted pooled area under the receiver operating characteristic curve (AUC) with 95% confidence intervals (CIs), heterogeneity statistics, and participant numbers. Certainty of evidence was graded using GRADE criteria.
Results: Our analysis included ten studies (seven on AD, four on PD; 496 patients, 441 patients, and 36,990 healthy controls). The overall pooled AUC was 0.73 (95% CI, 0.69-0.77; I²=78%). Subgroup analyses showed an AUC of 0.72 for AD and 0.70 for PD. QUADAS-2 assessments indicated low-to-moderate risk of bias, with patient selection variability being a key concern. GRADE evaluations showed moderate to high certainty in the evidence.
Conclusions: AI‑assisted retinal imaging demonstrates consistent, moderate accuracy for early detection of AD and PD. Future research should standardize imaging protocols and patient selection criteria, and pursue large-scale, prospective validation.
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http://dx.doi.org/10.1016/j.pdpdt.2025.104788 | DOI Listing |
Eye (Lond)
September 2025
Department of Ophthalmology, All India Institute of Medical sciences, Bhubaneswar, Odisha, India.
Eur J Cancer
August 2025
Emory University, Atlanta, USA; Wallace H. Coulter Department of Biomedical Engineering, Georgia Institute of Technology and Emory University, Atlanta, GA, USA; Atlanta Veterans Administration Medical Center, Atlanta, USA. Electronic address:
Background: Early detection of hematological malignancies improves long-term survival but remains a critical challenge due to heterogeneity in clinical presentation. Chronic inflammation is a key driver in hematologic cancers and is known to induce compensatory microvascular changes. High-resolution, non-invasive retinal imaging can allow the quantification of microvascular changes for the early detection of hematological malignancies.
View Article and Find Full Text PDFNeurol Neuroimmunol Neuroinflamm
November 2025
Departments of Neurology and Ophthalmology, NYU Grossman School of Medicine, NY; and.
Background And Objectives: While reductions in optical coherence tomography (OCT) pRNFL and ganglion cell-inner plexiform layer thicknesses have been shown to be associated with brain atrophy in adult-onset MS (AOMS) cohorts, the relationship between OCT and brain MRI measures is less established in pediatric-onset MS (POMS). Our aim was to examine the associations of OCT measures with volumetric MRI in a cohort of patients with POMS to determine whether OCT measures reflect CNS neurodegeneration in this patient population, as is seen in AOMS cohorts.
Methods: This was a cross-sectional study with retrospective ascertainment of patients with POMS evaluated at a single center with expertise in POMS and neuro-ophthalmology.
Retina
September 2025
Department of Ophthalmology, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse 15, CH-3010.
Purpose: To evaluate inter-grader variability in posterior vitreous detachment (PVD) classification in patients with epiretinal membrane (ERM) and macular hole (MH) on spectral-domain optical coherence tomography (SD-OCT) and identify challenges in defining a reliable ground truth for artificial intelligence (AI)-based tools.
Methods: A total of 437 horizontal SD-OCT B-scans were retrospectively selected and independently annotated by six experienced ophthalmologists adopting four categories: 'full PVD', 'partial PVD', 'no PVD', and 'ungradable'. Inter-grader agreement was assessed using pairwise Cohen's kappa scores.
Retina
September 2025
Retina Division, Stein Eye Institute, University of California of Los Angeles, Los Angeles, California.
Purpose: To describe the clinical and multimodal imaging features of a novel form of macular neovascularization (MNV), designated Type 4 MNV, defined by mixed Type 1 and Type 2 neovascularization (NV), extensive intraretinal anastomotic NV, and central posterior hyaloid fibrosis (CPHF).
Methods: This multicenter retrospective observational case series included patients with neovascular age-related macular degeneration (AMD) exhibiting both Type 1 and 2 MNV and an overlying anastomotic intraretinal NV network. This was confirmed with OCT and OCT angiography (OCTA).