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In-vivo iron mapping in patients with Parkinson's disease using deep learning-based susceptibility source separation MRI.

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The authors' code

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  1. # chi-separation toolbox (*χ*-separation, x-separation)
  2. * ⭐ Toolbox version 1.2.2 is released!
  3. * ⭐ A download link for Toolbox version 1.2.2 will be sent to your email once you submit the Google Form: https://forms.gle/nhJahF86zpMgEKvM9
  4. * ⭐ This toolbox is developed for in-vivo human 3T and 7T datasets. Other field stengths, high resolution ex-vivo or nonhuman datasets (< 0.6 mm) are not fully tested and may require additional processing.
  5. * ⭐ E-mail us if you need data processing other than in-vivo human 3T datasets. We may be able to help you with scan protocol and processing.
  6. * ⭐ If you have both GRE and SE data, you have data processing options of conventional optimization (MEDI, iLSQR) and neural network (chi-sepnet-R2', better quality).
  7. * ⭐ If you only have GRE data, neural network (chi-sepnet-R2*) will deliver high quality *&chi;*-separation maps.
  8. * ⭐ Neural networks can process resolution > 0.6 mm. This makes high resolution ex-vivo or rodent data processing difficult if you only have GRE data.
  9. * The *&chi;*-separation toolbox includes the following features:
  10. - DICOM/NIFTI data compatibility
  11. - **QSMnet**: Quantitative susceptibility mapping (QSM) reconstruction algorithm based on deep neural network (QSMnet; J. Yoon et al., Neuroimage, 2018)
  12. - **_&chi;_-separation using _R_<sub>2</sub>' (or _R_<sub>2</sub>\* )**: Magnetic susceptibility source separation algorithms based on convex optimization (*&chi;*-separation; H. Shin et al., Neuroimage, 2021) that share similar contrasts and optimization parameters with either MEDI+0 (Liu et al., MRM, 2018) or iLSQR (Li et al., Neuroimage, 2015) algorithms. The toolbox also provides the option to use pseudo *R*<sub>2</sub> map if *R*<sub>2</sub> measurement is not availabe (using *R*<sub>2</sub>' is reconmmanded for accurate estimation).
  13. - **_&chi;_-sepnet using _R_<sub>2</sub>' (or _R_<sub>2</sub>\* )**: A U-Net-based neural network that reconstructs COSMOS-quality *&chi;*-separation using *R*<sub>2</sub>' and phase. In case *R*<sub>2</sub> is not measured, another neural network is trained to estimate *&chi;*-separation maps from *R*<sub>2</sub>\* and phase.
  14. - The toolbox also supports phase preprocessing (e.g. phase unwrapping and background removal) powered by MEDI, STI Suite, SEGUE, and mritools toolboxs (see the Chisep_script.m file for details).
  15. * Last update: June-03-2026 (Taechang Kim, Hyeong-Geol Shin)
  16. ## Requirements
  17. * MATLAB version (tested in R2021a-R2026a. Toolbox will fail any version before R2021a.)
  18. * MATLAB Add-Ons:
  19. - Image Processing Toolbox, Signal Processing Toolbox, Parallel Computing Toolbox, Statistics and Machine Learning Toolbox, Deep Learning Toolbox
  20. - For QSMnet and *&chi;*-sepnet, Deep Learning MATLAB Toolbox Converter for ONNX Model Format (https://www.mathworks.com/matlabcentral/fileexchange/67296-deep-learning-toolbox-converter-for-onnx-model-format)
  21. ## Recommendation for acquisition
  22. * Multiecho GRE data for in-vivo
  23. - TR = 33 ms; TE1 = 5 ms; Echo spacing = 6 ms; Number of echoes = 5; flip angle = 15° Matrix size (AP LR HF) = 256 x 176 x 144 Resolution = isotropic 1 mm Parallel imaging factor = 2; elliptical k-space shutter Acquisition time = 6 mins.
  24. - Follow QSM consensus paper (https://doi.org/10.1002/mrm.30006)
  25. * Multiecho SE data for in-vivo
  26. - TBA
  27. * Multiecho GRE data for high resolution ex-vivo
  28. - Highly recommend to acquire multi-orientation data (relative to B0).
  29. ## Recommendation for data analysis
  30. * *&chi;*-separation template and regions of interest are available here [[link](https://github.com/SNU-LIST/chi-separation-atlas)]
  31. * K Min et al. A human brain atlas of *&chi;*-separation for normative iron and myelin distributions. NMR Biomed, 2024 online [[link](https://doi.org/10.1002/nbm.5226)]
  32. ## Reference
  33. * H. Shin, J. Lee, Y. H. Yun, S. H. Yoo, J. Jang, S.-H. Oh, Y. Nam, S. Jung, S. Kim, F. Masaki, W. Kim, H. J. Choi, J. Lee. *&chi;*-separation: Magnetic susceptibility source separation toward iron and myelin mapping in the brain. Neuroimage, 2021 Oct; 240:118371.
  34. ## Contacts
  35. * [email hidden]
  36. * [email hidden] (Hyeong-Geol Shin, PhD)
  37. * [email hidden] (Taechang Kim, PhD student @ SNU-LIST)

README.md at commit 29f901c, no license · at the source

Overview

Authors: Hyeong-Geol Shin1,2, Kelly A Mills2, Ted M Dawson2,3,4,5, Taechang Kim6, Jongho Lee6, Xu Li1,7, Peter van Zijl1,7, Jannik Prasuhn1,2,8,9,10
  1. F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD USA
  2. Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, MD USA
  3. Neuroregeneration and Stem Cell Programs, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD USA
  4. Department of Physiology, Pharmacology and Therapeutics, Johns Hopkins University School of Medicine, Baltimore, MD USA
  5. Solomon H. Snyder Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD USA
  6. Department of Electrical and Computer Engineering, Seoul National University, Seoul, Republic of Korea
  7. Division of MR Research, Department of Radiology, Johns Hopkins University School of Medicine, Baltimore, MD USA
  8. Section of Movement Disorders, Department of Neurology, University Medical Center Schleswig-Holstein, Campus Lübeck, Lübeck, Germany
  9. Institute of Neurogenetics, University of Lübeck, Lübeck, Germany
  10. Center for Brain, Behavior and Metabolism, University of Lübeck, Lübeck, Germany
Institutions: Kennedy Krieger Institute (United States); Johns Hopkins University (United States); Johns Hopkins Medicine (United States); Seoul National University (South Korea); University of Lübeck (Germany)
Journal: NPJ Parkinson's disease, volume 12, issue 1, article 200
Dates: received 2 November 2025; accepted 29 April 2026; published online 27 May 2026
Type: Research article · Language: English
License: CC BY
Identifiers: DOI 10.1038/s41531-026-01384-x · PMID 42204172 · PMCID PMC13493794 · OpenAlex W7162552902
Open access: gold, a free copy (OpenAlex)
Status: empty repository
Categories: structural MRI / diffusion (modality), human (organism), Parkinson's (population), clinical / translational (subfield)
Methods: Statistics, Smoothing, state filtering, decompositions, Connectivity, Machine learning, fMRI & imaging
Keywords: Computational biology and bioinformatics, Diseases, Neurology, Neuroscience
Topic: Parkinson's Disease Mechanisms and Treatments (Neurology, Medicine), according to OpenAlex
Funding: National Institutes of Health (P41EB031771); NIH HHS (P41EB031771); NIBIB NIH HHS (P41 EB031771); Thiemann Stiftung
Citations: not cited yet (Europe PMC); 52 references in the paper

Abstract

Parkinson’s disease (PD) involves pathological iron accumulation, yet MRI metrics, such as R2* or magnetic susceptibility (χ), lack mechanistic specificity because they convolve paramagnetic and diamagnetic sources. We applied an AI-assisted χ-separation framework that combines deep learning (DL)-based preprocessing with biophysical modeling to assess paramagnetic iron with enhanced specificity. Twenty-five PD patients and twenty-six matched controls underwent 3 T multi-parametric MRI. DL-based χ-separation (χ-separationDL) separated the paramagnetic susceptibility component (χpara; indicative of iron) from χ, revealing alterations undetected by established susceptibility-based methods: χpara increased in dorsal premotor cortex ( +6.3%, P = 0.032) and substantia nigra pars compacta ( +10.2%, P = 0.024), χpara in premotor cortex correlated with disease duration (r = 0.41; P = 0.045). DL-based preprocessing was not inferior for the differentiation between PD patients vs. controls compared to established optimization-based χ-separation, indicating the potential for AI-enhanced χ-separation to be applied within the scope of susceptibility imaging in PD.

Reproduced under the paper's license (CC BY), from the paper cited above.

Repository

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SNU-LIST/chi-separation

License: none: the authors keep all their rights
State: the link answers, verified on 26 September 2026
Evidence: files inventoried
Commit: 29f901c39c70cf71eca4ba46cd8da2a67d16d874, 3 June 2026
Size: 1 file, 0 scripts
Software Heritage: not archived
Found in: the text, “MRI postprocessing and analyses”
Holds: README
Not found: license file, CITATION.cff, environment file, tests, continuous integration, documentation
Availability: 1 check, the latest on 26 September 2026: the link answers
  • 26 September 2026: the link answers
1 file

Code availability

The code used for the analyses in this study is available from the corresponding author upon reasonable request.

Reproduced under the paper's license (CC BY), from the paper cited above.

Tracing map

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Data

No dataset and no data link were found in the paper.

Data Availability

The datasets generated and/or analyzed during the current study are not publicly available due to data protection regulations and institutional ethics restrictions, as the data contain potentially identifiable clinical and imaging information. However, the datasets are available from the corresponding author on reasonable request and subject to approval by the responsible ethics committee and data transfer agreements in accordance with applicable data protection laws (including GDPR).

Reproduced under the paper's license (CC BY), from the paper cited above.

Versions

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Version 1, 28 September 2026: the first record

Recorded: type, language, journal, volume, issue, pages, dates, 8 authors, 4 keywords, 4 funders, 52 references.

Cite

This paper

Shin, H.-G., Mills, K. A., Dawson, T. M., Kim, T., Lee, J., Li, X., van Zijl, P., & Prasuhn, J. (2026). In-vivo iron mapping in patients with Parkinson's disease using deep learning-based susceptibility source separation MRI. NPJ Parkinson's disease, 12(1), 200. https://doi.org/10.1038/s41531-026-01384-x

BibTeX

@article{shin2026vivo,
author = {Shin, Hyeong-Geol and Mills, Kelly A and Dawson, Ted M and Kim, Taechang and Lee, Jongho and Li, Xu and van Zijl, Peter and Prasuhn, Jannik},
title = {{In-vivo iron mapping in patients with Parkinson's disease using deep learning-based susceptibility source separation MRI}},
journal = {NPJ Parkinson's disease},
year = {2026},
month = may,
volume = {12},
number = {1},
pages = {200},
publisher = {Nature Publishing Group},
issn = {2373-8057},
doi = {10.1038/s41531-026-01384-x},
url = {https://doi.org/10.1038/s41531-026-01384-x},
pmid = {42204172},
pmcid = {PMC13493794}
}

RIS

TY - JOUR
AU - Shin, Hyeong-Geol
AU - Mills, Kelly A
AU - Dawson, Ted M
AU - Kim, Taechang
AU - Lee, Jongho
AU - Li, Xu
AU - van Zijl, Peter
AU - Prasuhn, Jannik
TI - In-vivo iron mapping in patients with Parkinson's disease using deep learning-based susceptibility source separation MRI
T2 - NPJ Parkinson's disease
J2 - NPJ Parkinsons Dis
PY - 2026
DA - 2026/05/27
VL - 12
IS - 1
SP - 200
SN - 2373-8057
PB - Nature Publishing Group
DO - 10.1038/s41531-026-01384-x
UR - https://doi.org/10.1038/s41531-026-01384-x
LA - en
ER -

CSL-JSON

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