mlsanityData to 7 Oct 2026

PEPSI: Pathology-Enhanced Pulse-Sequence-Invariant Representations for Brain MRI

arXiv 2403.06227 ↗First posted 10 Mar 2024eess.IV cs.CVcited by 8

Not on the map. Why?

Abstract (arXiv)

Remarkable progress has been made by data-driven machine-learning methods in the analysis of MRI scans. However, most existing MRI analysis approaches are crafted for specific MR pulse sequences (MR contrasts) and usually require nearly isotropic acquisitions. This limits their applicability to diverse real-world clinical data, where scans commonly exhibit variations in appearances due to being obtained with varying sequence parameters, resolutions, and orientations -- especially in the presence of pathology. In this paper, we propose PEPSI, the first pathology-enhanced, and pulse-sequence-invariant feature representation learning model for brain MRI. PEPSI is trained entirely on synthetic images with a novel pathology encoding strategy, and enables co-training across datasets with diverse pathologies and missing modalities. Despite variations in pathology appearances across different MR pulse sequences or the quality of acquired images (e.g., resolution, orientation, artifacts, etc), PEPSI produces a high-resolution image of reference contrast (MP-RAGE) that captures anatomy, along with an image specifically highlighting the pathology. Our experiments demonstrate PEPSI's remarkable capability for image synthesis compared with the state-of-the-art, contrast-agnostic synthesis models, as it accurately reconstructs anatomical structures while differentiating between pathology and normal tissue. We further illustrate the efficiency and effectiveness of PEPSI features for downstream pathology segmentations on five public datasets covering white matter hyperintensities and stroke lesions. Code is available at https://github.com/peirong26/PEPSI.

Key facts. Cited by 8 papers in the map (data through 7 Oct 2026). Builds on 19 of its 31 references that are in the map. First posted on arXiv 10 Mar 2024.

Builds on

19 of 31 references.

References · 19

  1. 2020Language Models are Few-Shot Learnerscited by 32,199
  2. 2015U-Net: Convolutional Networks for Biomedical Image Segmentationcited by 19,604
  3. 2023Segment Anythingcited by 8,158
  4. 2022PaLM: Scaling Language Modeling with Pathwayscited by 5,304
  5. 2021On the Opportunities and Risks of Foundation Modelscited by 3,961
  6. 2022Large Language Models Encode Clinical Knowledgecited by 1,807
  7. 2018Deep Visual Domain Adaptation: A Surveycited by 634
  8. 2022MONAI: An open-source framework for deep learning in healthcarecited by 438
  9. 2023Towards Generalist Biomedical AIcited by 286
  10. 2021SynthSeg: Segmentation of brain MRI scans of any contrast and resolution without retrainingcited by 235
  11. 2020SynthMorph: learning contrast-invariant registration without acquired imagescited by 137
  12. 2022SynthStrip: Skull-Stripping for Any Brain Imagecited by 126
7 more
  1. 2023Foundational Models Defining a New Era in Vision: A Survey and Outlookcited by 109
  2. 2022ISLES 2022: A multi-center magnetic resonance imaging stroke lesion segmentation datasetcited by 104
  3. 2020Joint super-resolution and synthesis of 1 mm isotropic MP-RAGE volumes from clinical MRI exams with scans of different orientation, resolution and contrastcited by 45
  4. 2023Quantifying white matter hyperintensity and brain volumes in heterogeneous clinical and low-field portable MRIcited by 15
  5. 2020Discovering Hidden Physics Behind Transport Dynamicscited by 8
  6. 2021Deep Decomposition for Stochastic Normal-Abnormal Transportcited by 4
  7. 2021Differential Motion Evolution for Fine-Grained Motion Deformation in Unsupervised Image Animationcited by 3

Built on by

Cited by year

Citing papers per year: 2024: 3; 2025: 5.

8 papers.