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Brain foundation models with hypergraph dynamic adapter for brain disease analysis

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Peer-reviewed

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Abstract

Brain diseases, such as Alzheimer’s disease and brain tumors, present profound challenges due to their complexity and societal impact. Recent advancements in brain foundation models have shown significant promise in addressing a range of brain-related tasks. However, current brain foundation models are limited by task and data homogeneity, restricted generalization beyond segmentation or classification, and inefficient adaptation to diverse clinical tasks. In this work, we propose SAM-Brain3D, a brain-specific foundation model trained on over 66,000 brain image-label pairs across 14 MRI sub-modalities, and Hypergraph Dynamic Adapter (HyDA), a lightweight adapter for efficient and effective downstream adaptation. SAM-Brain3D captures detailed brain-specific anatomical and modality priors for segmenting diverse brain targets and broader downstream tasks. HyDA leverages hypergraphs to fuse complementary multi-modal data and dynamically generate patient-specific convolutional kernels for multi-scale feature fusion and personalized patient-wise adaptation. Together, our framework excels across a broad spectrum of brain disease segmentation and classification tasks. Extensive experiments demonstrate that our method consistently outperforms existing state-of-the-art approaches, offering a new paradigm for brain disease analysis through multi-modal, multi-scale, and dynamic foundation modeling.

Description

Journal Title

Pattern Recognition

Conference Name

Journal ISSN

0031-3203
1873-5142

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Publisher

Elsevier

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Except where otherwised noted, this item's license is described as Attribution 4.0 International
Sponsorship
Wellcome Trust (221633/Z/20/Z)
Biotechnology and Biological Sciences Research Council (BB/P021255/1)
Wellcome Trust (205067/Z/16/Z)
EPSRC (EP/V029428/1)
EPSRC (EP/S026045/1)
EPSRC (EP/T003553/1)
Engineering and Physical Sciences Research Council (EP/N014588/1)
EPSRC (EP/T017961/1)
Wellcome Trust (215733/Z/19/Z)
European Commission Horizon 2020 (H2020) Marie Sk?odowska-Curie actions (777826)
This project was supported with funding from the Cambridge Centre for Data-Driven Discovery and Accelerate Programme for Scientific Discovery, made possible by a donation from Schmidt Sciences. Zhongying Deng acknowledges the support from Wellcome Trust 221633/Z/20/Z. Zoe Kourtzi acknowledges support from the Biotechnology and Biological Sciences Research Council H012508 and BB/P021255/1, Alan Turing Institute TU/B/000095, Wellcome Trust 205067/Z/16/Z, 221633/Z/20/Z, Royal Society INF/R2/202107. Carola-Bibiane Schönlieb acknowledges support from the Philip Leverhulme Prize, the Royal Society Wolfson Fellowship, the EPSRC advanced career fellowship EP/V029428/1, EPSRC grants EP/S026045/1 and EP/T003553/1, EP/N014588/1, EP/T017961/1, the Wellcome Innovator Awards 215733/Z/19/Z and 221633/Z/20/Z, the European Union Horizon 2020 research and innovation programme under the Marie Skodowska-Curie grant agreement No. 777826 NoMADS, the Cantab Capital Institute for the Mathematics of Information and the Alan Turing Institute. Angelica I. Aviles-Rivero gratefully acknowledges the support from Yau Mathematical Sciences Center, Tsinghua University. Chaoyu Liu acknowledges the support from the Maths4DL program under grant EP/V026259/1.

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