Searcharxiv⌕ Search

arXiv · 2610.00553

Hetero-modal learning and corruption-resistant hetero-modal inference for joint segmentation of white matter hyperintensities and ischaemic stroke lesions in MRI

Abstract

White matter hyperintensities (WMH) and ischaemic stroke lesions (ISL) are visually confounding, co-occurring pathologies that require large, diverse datasets for robust deep learning segmentation. However, assembling such datasets is hindered by cohort samples that lack reference segmentations from both features and complete sets of MRI structural sequences (i.e., "modalities"). To maximise data utility, we investigate hetero-modal learning using a dataset of 206 vascular disease patients across four MRI sequences (T1-weighted, T2-weighted, fluid-attenuated inversion recovery, and diffusion-weighted imaging) with expert annotations of both WMH and ISL. We demonstrate that hetero-modal learning outperforms models trained using a single imaging modality in scenarios with substantial missing data, including a split where only 10% of the training data contains all four modalities while the remainder is uni-modal, and a split relying on a single shared "anchor" modality with zero overlap between the remaining modalities. Furthermore, models trained under this second split successfully perform inference on unseen combinations of modalities. Yet, while standard hetero-modal networks handle missing sequences, clinical deployment introduces the additional challenge of silent data degradation - where modalities are present but severely corrupted. To bridge this gap, we introduce the Multimodal Attention Router (MMAR) block. Our experiments demonstrate that, when trained with a "corruption augmentation" strategy, the MMAR effectively dynamically weights the encoded features of each modality, maintaining strong performance during hetero-modal inference even in the presence of unflagged catastrophically corrupted modalities.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Jesse Phitidis, William N. Whiteley, Joanna M. Wardlaw, Miguel O. Bernabeu, Francesco Dalla Serra, Maria del C. Valdés Hernández. 2026-09-30. Hetero-modal learning and corruption-resistant hetero-modal inference for joint segmentation of white matter hyperintensities and ischaemic stroke lesions in MRI. https://arxiv.org/abs/2610.00553

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Trajectory Stitching for Solving Inverse Problems with Flow-Based Models

Flow-based generative models have emerged as powerful priors for solving inverse problems. One option is to directly optimize the initial latent code (noise), such that the flow output solves the inverse problem. However, this requires backpropagating through the entire generative trajectory, incurring high memory costs and numerical instability. We propose MS-Flow, which represents the trajectory as a sequence of intermediate latent states rather than a single initial code. By enforcing the flow dynamics locally and coupling segments through trajectory-matching penalties, MS-Flow alternates between updating intermediate latent states and enforcing consistency with observed data. This reduces memory consumption while improving reconstruction quality. We demonstrate the effectiveness of MS-Flow over existing methods on image recovery and inverse problems, including inpainting, super-resolution, and computed tomography.

eess.IV↗

Rapid quantitative chemical composition mapping using model-based MRI reconstruction with field inhomogeneity correction

Magnetic resonance spectroscopic imaging methods are particularly attractive for chemical engineering applications, including the monitoring of chemical reactions, where a rapid assessment of spatial variations in chemical composition is required. Conventional approaches, such as chemical shift imaging, introduce an additional spectral-encoding dimension, which substantially increases acquisition time. Consequently, fast spatially resolved spectroscopy remains an active research topic. This work uses a model-based reconstruction framework that embeds a priori spectral knowledge of the involved chemical components into the forward model to accelerate composition mapping. It allows for the reconstruction of molar ratio maps for individual chemical components without acquiring high-resolution spectra. Extending from previous studies, the proposed model accounts for inhomogeneities of the main field, which become more pronounced in systems with larger bores relevant for process engineering. Phantom experiments employing a 2D multi-gradient echo sequence demonstrate the ability to determine molar ratios for chemical components with single peaks as well as multiple peaks in their spectra. The bias and precision of the method remain around 0.01 mol/mol and 0.09 mol/mol, respectively, for a 20 s scan, indicating suitability for dynamic processes. Finally, acquisition time can be reduced further by applying sparse k-space sampling, potentially shortening the scan to 5 s with only minor degradation in quantitative performance.

eess.IV↗

MorphoBranch: A Fine-Structure-Preserving Workbench for Morphometric Analysis of Branched Cellular Structures

Background and Objectives: Fluorescence-labeled cellular arbors provide readouts of neuronal and microglial morphology, but fine and weakly labeled processes are prone to fragmentation and false connections that bias skeleton-based measurements. We present MorphoBranch, a fine-structure-preserving, human-reviewable workbench for morphometry of branched cellular structures. Methods: MorphoBranch combines a deterministic Morphometry Engine with an LLM-assisted Refinement Engine. The Mor- phometry Engine implements an image-to-graph workflow integrating multiscale structural evidence extraction, hysteresis segmen- tation, evidence-constrained skeleton refinement, and graph-based morphometry. The Refinement Engine maps natural-language requests to registered actions for parameter adjustment, preview execution, metric reporting, and unsupported-request handling, while image processing and quantitative computation remain deterministic and reviewable. Results: MorphoBranch was evaluated on two public neuronal axon datasets, AxonMIP and AxonStack, and the in-house Cell- Morph dataset of microglial fluorescence images. It achieved the highest Skeleton F1 and clDice and the lowest length-estimation error among the evaluated methods on all three datasets, while also achieving the highest Dice and IoU on AxonMIP and Axon- Stack. Across 150 natural-language tasks, the Refinement Engine achieved a 94.0% end-to-end success rate. Conclusions: These results demonstrate that MorphoBranch provides a reproducible, human-reviewable workflow for mor- phometric analysis of branched cellular structures. It supports fine-structure-preserving quantification across neuronal axon and microglial fluorescence images while maintaining inspectable and reproducible analysis workflows.

eess.IV↗