Evidence map›Paper›PMID 42157271›Full record

ReviewInternational journal of retina and vitreous2026

Artificial intelligence and neurodegeneration: state of the art and explainability.

Emanuele Crincoli, Maria Cristina Savastano, Alfonso Savastano, Matteo Mario Carlà, Federico Giannuzzi, Fiammetta Catania, Raphael Kilian, Clara Rizzo, Stanislao Rizzo

Abstract readReview
In one paragraph

Review in International journal of retina and vitreous, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Emanuele CrincoliOphthalmology Unit, "Fondazione Policlinico Universitario A. Gemelli IRCCS", Catholic University "Sacro Cuore", Largo A. Gemelli 8 - 00198, Rome, Italy. emanuelecrincoli1@gmail.com.ORCID http://orcid.org/0000-0001-9996-9871
Maria Cristina SavastanoOphthalmology Unit, "Fondazione Policlinico Universitario A. Gemelli IRCCS", Catholic University "Sacro Cuore", Largo A. Gemelli 8 - 00198, Rome, Italy.
Alfonso SavastanoOphthalmology Unit, "Fondazione Policlinico Universitario A. Gemelli IRCCS", Catholic University "Sacro Cuore", Largo A. Gemelli 8 - 00198, Rome, Italy.
Matteo Mario CarlàOphthalmology Unit, "Fondazione Policlinico Universitario A. Gemelli IRCCS", Catholic University "Sacro Cuore", Largo A. Gemelli 8 - 00198, Rome, Italy.
Federico GiannuzziOphthalmology Unit, "Fondazione Policlinico Universitario A. Gemelli IRCCS", Catholic University "Sacro Cuore", Largo A. Gemelli 8 - 00198, Rome, Italy.
Fiammetta CataniaDepartement d'Ophtalmologie, Hopital Fondation Adolphe De Rothschild, 29 Rue Manin, Paris, 75019, France.
Raphael KilianDepartement of Translational Medicine, University of Ferrara, Ferrara, Italy.
Clara RizzoOphthalmic Unit, Department of Neurosciences, Biomedicine and Movement Sciences, University of Verona, 37219, Verona, Italy.
Stanislao RizzoOphthalmology Unit, "Fondazione Policlinico Universitario A. Gemelli IRCCS", Catholic University "Sacro Cuore", Largo A. Gemelli 8 - 00198, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlzheimer disease (AD) and Parkinson disease (PD) are an increasing healthcare concern and growing cause of disability in our century. The advent of the artificial intelligence (AI) era and the early changes in retina and optic nerve morphology detected in neurodegenerative diseases by recent literature opened the way to the perspective of a AI-based diagnosis for both conditions. MAIN BODY: In AD a generalized decrease in macular Ganglion Cells-Inner Plexiform Layer (GC-IPL) and retinal nerve fiber layer (RNFL) and peripapillary RNFL thickness has been documented. Moreover, clinical AD is characterized by a lower choroidal thickness and higher choroidal vascularity index. AI can be predicted with around 80% accuracy based on small fundus vessels characteristics. Similarly, AI based on Optical Coherence Tomography (OCT) images showed very good performance in detecting AD, especially based on total macular volume (TVM) and GCL thickness. A combination of OCT and color fundus photographs (CFP) imaging reached 85% accuracy in detecting MCI. In PD typical retinal anomalies include a generalized thinning of the peripapillary RNFL with a degeneration pattern similar to the one of mitochondrial optic neuropathies, foveal pit widening, generalized retinal and retinal pigmented epithelium thinning and outer plexiform layer thickening. AI CFP-based detection of PD showed only 65% accuracy due to a low specificity, while multimodal imaging-based AI was the best approach, reaching a 100% sensitivity and 85% specificity.

conclusionIn consideration of the overall very good performance, AD and PD are likely to benefit from the support of retinal-imaging based AI for early diagnosis. To optimize the performance, especially in terms of specificity, the use of multimodal imaging and possible integration with meta-data has been demonstrated to be the best technique, especially for PD diagnosis. However, training and testing on a larger sample size and longitudinal evaluation of the chosen models will be needed before application on general population. So far, explainability of the proposed models seems robust and coherent with the corresponding central nervous system damage.

Indexed as

AlzheimerArtificial intelligenceColor fundus photographDeep learningExplainabilityNeurodegenerationOculomicsOptical coherence tomographyParkinsonRetina

Identifiers

PMID42157271
PMCPMC13366837

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Registered trials

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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.