Evidence map›Paper›PMID 42078464›Full record

ArticleFrontiers in medicine2026

How well do frozen foundation models transfer? A calibration-focused benchmark for diabetic retinopathy grading.

Mehmet Poyrazer, Hüseyin Yağcı, Rıdvan Erten

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Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Mehmet PoyrazerDivision of Endocrinology and Metabolism, University of Health Sciences Ankara Training and Research Hospital, Ankara, Türkiye.
Hüseyin YağcıDivision of Endocrinology and Metabolism, University of Health Sciences Ankara Training and Research Hospital, Ankara, Türkiye.
Rıdvan ErtenDivision of Geriatrics, Department of Internal Medicine, Faculty of Medicine, Kocaeli University, Kocaeli, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Pretrained foundation models are increasingly adopted for diabetic retinopathy (DR) screening, yet it remains unclear how much of their performance derives from the learned representations versus the adaptation procedure. Most benchmarks report discrimination metrics alone, neglecting probability calibration. Methods: We compared the frozen representations of three pretrained encoders: MedSigLIP (medical vision-language; ViT-B/16, 448 × 448), RETFound (retinal self-supervised; ViT-L/16, 224 × 224), and EfficientNet-B0 (ImageNet-supervised; 224 × 224). All encoder weights were frozen; only an identical lightweight multilayer perceptron head was trained. Models were developed on APTOS 2019 (3,662 fundus images; five-fold cross-validation) and externally validated on MESSIDOR-2 (1,744 images). Binary referable DR detection and five-class severity grading were evaluated. AUC, expected calibration error (ECE), and Brier score served as co-primary endpoints. External-set tests used patient-level cluster-robust bootstrap to account for bilateral correlation. Results: On the development set, all three encoders achieved near-identical binary AUC (0.980-0.985). MedSigLIP showed superior calibration, with a lower Brier score than RETFound (0.044 vs. 0.049; Conclusion: Under frozen transfer, the MedSigLIP encoder package produced more generalisable and better calibrated representations than both retinal self-supervised (RETFound) and ImageNet-supervised (EfficientNet-B0) encoders. Domain-specific pretraining did not guarantee domain-general frozen representations. These findings demonstrate that development-set discrimination alone is insufficient for encoder evaluation and that calibration metrics-particularly the Brier score-should be reported as standard practice.

Indexed as

calibrationdiabetic retinopathydomain shiftexternal validationfoundation modelsfrozen encoderrepresentation transfertemperature scaling

Identifiers

PMID42078464
PMCPMC13128382

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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.