ArticleResearch square2025
Deep Learning Detection of Retinitis Pigmentosa Inheritance Forms through Synthetic Data Expansion of a Rare Disease Dataset.
Article in Research square, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
- Updated by
Authors and funding
10 authors.
Funding
Abstract
Accurate classification of inheritance patterns is an integral part of diagnosis and genetic counseling for inherited retinal diseases (IRDs). Traditionally reliant on pedigree analysis, clinical phenotyping, and genetic testing, this process is often constrained by incomplete family history, ambiguous presentations, limited access to genetic testing, and inconclusive genetic test results. Deep learning (DL) applied to fundus imaging presents a promising approach for automated inference of inheritance modes; however, development has been hindered by the low prevalence of IRDs and the scarcity of annotated datasets. In this study, we focus on retinitis pigmentosa (RP), a highly heterogeneous disorder in both clinical presentation and genetic etiology. We present a first-in-class deep learning approach that leverages Vision Transformer (ViT) models to distinguish autosomal from X-linked RP using color fundus photography. To overcome challenges posed by limited data, we introduce an innovative variational autoencoder-based data expansion strategy, which improves inheritance pattern classification based on color fundus photos from 0.67 AUC to 0.79 AUC. Our findings demonstrate the potential of deep learning to uncover subtle phenotypic differences linked to genetic inheritance and introduce a novel training data augmentation method to render deep learning accessible to rare diseases.
Identifiers
What OpenQuestion holds
Registered trials
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.