Sam Hashemi

2papers

2 Papers

29.5CVApr 13
Towards Brain MRI Foundation Models for the Clinic: Findings from the FOMO25 Challenge

Asbjørn Munk, Stefano Cerri, Vardan Nersesjan et al.

Clinical deployment of automated brain MRI analysis faces a fundamental challenge: clinical data is heterogeneous and noisy, and high-quality labels are prohibitively costly to obtain. Self-supervised learning (SSL) can address this by leveraging the vast amounts of unlabeled data produced in clinical workflows to train robust \textit{foundation models} that adapt out-of-domain with minimal supervision. However, the development of foundation models for brain MRI has been limited by small pretraining datasets and in-domain benchmarking focused on high-quality, research-grade data. To address this gap, we organized the FOMO25 challenge as a satellite event at MICCAI 2025. FOMO25 provided participants with a large pretraining dataset, FOMO60K, and evaluated models on data sourced directly from clinical workflows in few-shot and out-of-domain settings. Tasks covered infarct classification, meningioma segmentation, and brain age regression, and considered both models trained on FOMO60K (method track) and any data (open track). Nineteen foundation models from sixteen teams were evaluated using a standardized containerized pipeline. Results show that (a) self-supervised pretraining improves generalization on clinical data under domain shift, with the strongest models trained \textit{out-of-domain} surpassing supervised baselines trained \textit{in-domain}. (b) No single pretraining objective benefits all tasks: MAE favors segmentation, hybrid reconstruction-contrastive objectives favor classification, and (c) strong performance was achieved by small pretrained models, and improvements from scaling model size and training duration did not yield reliable benefits.

CVNov 21, 2025
An Artificial Intelligence Framework for Measuring Human Spine Aging Using MRI

Roozbeh Bazargani, Saqib Abdullah Basar, Daniel Daly-Grafstein et al.

The human spine is a complex structure composed of 33 vertebrae. It holds the body and is important for leading a healthy life. The spine is vulnerable to age-related degenerations that can be identified through magnetic resonance imaging (MRI). In this paper we propose a novel computer-vison-based deep learning method to estimate spine age using images from over 18,000 MRI series. Data are restricted to subjects with only age-related spine degeneration. Eligibility criteria are created by identifying common age-based clusters of degenerative spine conditions using uniform manifold approximation and projection (UMAP) and hierarchical density-based spatial clustering of applications with noise (HDBSCAN). Model selection is determined using a detailed ablation study on data size, loss, and the effect of different spine regions. We evaluate the clinical utility of our model by calculating the difference between actual spine age and model-predicted age, the spine age gap (SAG), and examining the association between these differences and spine degenerative conditions and lifestyle factors. We find that SAG is associated with conditions including disc bulges, disc osteophytes, spinal stenosis, and fractures, as well as lifestyle factors like smoking and physically demanding work, and thus may be a useful biomarker for measuring overall spine health.