ArticleEULAR rheumatology open2026
Artificial intelligence for automated classification of antinuclear-antibody indirect immunofluorescence patterns.
Article in EULAR rheumatology open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
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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
1 citing paper in PubMed.
- Deep learning for automated classification of antinuclear antibody patterns on HEp-2 indirect immunofluorescence images.Immunologic research · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Objectives: This study aims to interpret antinuclear-antibody indirect immunofluorescence (ANA-IIF) patterns using a multistage deep learning (DL) classification framework. Methods: A prospective, observational investigation was conducted over 18 months, aiming to develop and validate algorithms for classifying ANA-IIF patterns (N = 803), focusing on positive samples with International Consensus on Antinuclear Antibody Patterns standard patterns AC-1 to AC-5 and negative samples, while excluding mixed or nonconsensual patterns. Eight convolutional neural network (CNN) architectures were benchmarked against a multistage DL classification framework, where it first classifies an image into positive vs negative patterns, then metaphase stained vs not stained, and finally subclassifications within the stained and not-stained groups. All models were trained and evaluated using a 90:10 train-test split with 5-fold cross validation. Results: The multistage YOLOv8 pretrained models showed strong performance at each stage, achieving accuracies of 98.02% ± 0.49%, 96.57% ± 0.57%, 87.22% ± 1.11% (stained group), and 92.35% ± 1.5% (not-stained group), with an overall accuracy of 92.27 ± 1.01. In comparison, the multiclass YOLOv8 pretrained model achieved an overall accuracy of 87.16% ± 1.0%. The multistage YOLOv8 model consistently outperformed the other CNN architectures, reaching an average accuracy difference of 45.86 ± 1.25. Conclusions: This study demonstrates the advantage of multistage physician-centric design and implementation of a DL model for antinuclear antibody (ANA) pattern classification, particularly using advanced models like YOLO-v8. The hierarchical multistage approach offers a robust solution to the complexity inherent in ANA diagnostics, showing superior performance compared to other CNN architectures and a multiclass single model/classifier.
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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.