Releases: data-others/disease
3T Diffusion MRI Inter-Site Reproducibility Dataset for Cerebral Small Vessel Disease
CADASIL patients scanned on Siemens Prisma and Skyra within 24 hours
data-others/intersite-svd
This dataset provides inter-site / inter-scanner diffusion MRI from 10 patients with CADASIL, a genetically defined cerebral small vessel disease (SVD). Each participant was scanned on two different 3 Tesla Siemens MRI scanners — Magnetom Prisma and Magnetom Skyra — within less than 24 hours.
The dataset was created to evaluate the reproducibility of diffusion-derived metrics across scanners and is intended to support methodological development, clinical translation, and multi-center trial preparation in cerebral small vessel disease.
Dataset Overview
- Title: 3T diffusion MRI inter-site reproducibility dataset for cerebral small vessel disease
- Alternative titles:
- Intersite-SVD
- Interscanner-SVD
- Subjects: 10 CADASIL patients
- Condition: Cerebral small vessel disease (CADASIL)
- Design: Same subjects scanned on 2 scanners within <24 hours
- Data type: Diffusion MRI only
- Format: NIfTI, organized in BIDS format
- Archive:
intersite-svd.zip - Size: 11.1 GB
Terms of Use
This dataset is provided under the:
Creative Commons Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)
It may be freely downloaded and used for non-commercial purposes. Use of the dataset should acknowledge the associated Neurology paper.
Scientific Motivation
Diffusion MRI metrics are widely used as sensitive markers of microstructural tissue damage in cerebral small vessel disease. For these measures to be useful in clinical routine and multi-center trials, they need to be reproducible across scanners and sites.
This dataset addresses that need by providing a controlled within-subject comparison across two 3T scanners located in separate buildings with independent infrastructure at the same hospital.
The dataset has already been used in:
Konieczny & Dewenter et al., Neurology (2020)
https://doi.org/10.1212/WNL.0000000000011213
Participants
Participants were recruited at the Institute for Stroke and Dementia Research, Munich, Germany.
Cohort summary
- n = 10
- Diagnosis: CADASIL, confirmed by molecular genetic testing or skin biopsy
Clinical characteristics
| Characteristic | Value |
|---|---|
| Age, median (IQR) | 55.5 (13.3) years |
| Female | 5 (50%) |
| Hypertension | 3 (30%) |
| Hypercholesterolaemia | 5 (50%) |
| Diabetes | 0 (0%) |
| Current or past smoking | 3 (30%) |
| WMH volume [% ICV], median (IQR) | 7.67 (2.62) |
| Lacune count, median (IQR) | 3 (7.75) |
| Lacune volume [% ICV], median (IQR) | 0.01 (0.02) |
| Microbleed count, median (IQR) | 0.5 (1.75) |
| Brain volume [% ICV], median (IQR) | 75.7 (7.03) |
Abbreviations:
ICV = intracranial volume
IQR = interquartile range
WMH = white matter hyperintensities
MRI Acquisition
Participants were scanned on two Siemens 3T systems at LMU University Hospital:
- Siemens Magnetom Skyra
- Siemens Magnetom Prisma
The scanners were in separate buildings, which is why the dataset is treated as inter-site despite being from the same hospital.
Key protocol parameters were harmonized across scanners, including:
- b-values
- number of diffusion directions
- spatial resolution
Because the Skyra has a weaker gradient system, it required longer TE and TR.
MRI protocol comparison
| Parameter | Magnetom Skyra | Magnetom Prisma |
|---|---|---|
| Coil channels | 64 (head-neck) | 64 (head-neck) |
| TR [ms] | 3800 | 3200 |
| TE [ms] | 104.8 | 74 |
| Flip angle [°] | 90 | 90 |
| In-plane resolution [mm] | 2 × 2 | 2 × 2 |
| Slice thickness [mm] | 2 | 2 |
| Base resolution | 120 | 120 |
| Number of slices | 75 | 75 |
| b-values [s/mm²] | 1000 / 2000 | 1000 / 2000 |
| Directions per b-value | 30 / 60 | 30 / 60 |
| b=0 images | 10 | 10 |
| Receiver bandwidth [Hz/px] | 1894 | 1954 |
| Parallel imaging factor | 2 | 2 |
| Multi-band factor | 3 | 3 |
Data Organization
The dataset is stored in NIfTI format and follows the BIDS standard.
bval and bvec files follow FSL convention.
Included data
- Raw diffusion MRI
- converted from DICOM using
dcm2niix
- converted from DICOM using
- Preprocessed diffusion MRI
- processed as described in the manuscript
Directory structure
/sub-01
/ses-prisma
/dwi_raw
/dwi_preprocessed
/ses-skyra
/dwi_raw
/dwi_preprocessed
Diffusion Kurtosis MRI (DKI) Dataset – MCI and Cognitively Normal Controls
Fast Kurtosis Imaging (Sequence 139) with T1-weighted MRI
This dataset provides diffusion kurtosis MRI (DKI) acquired using a fast kurtosis sequence (the 139 sequence) together with T1-weighted structural MRI from 44 patients with mild cognitive impairment (MCI) and 23 cognitively normal controls. The T1-weighted images have been skull-stripped for anonymity.
The dataset is suitable for studies of microstructural alterations in early cognitive decline and for development or benchmarking of diffusion kurtosis processing pipelines.
Dataset Overview
- Title: Diffusion kurtosis MRI dataset
- DOI: https://doi.org/10.6084/m9.figshare.30850301
- Release date: 2025-12-10
- Author: Simon Eskildsen
- Total size: ~385.84 MB
Participants
- MCI patients: 44
- Cognitively normal controls: 23
- Total subjects: 67
Modalities
- Diffusion kurtosis MRI (DKI)
- T1-weighted MRI (skull-stripped)
Data Organization
-
DKI images:
Provided as separate NIfTI files, one file per diffusion direction. -
b-values and b-vectors:
Stored as text files in the same folders as the diffusion images. -
Structural MRI:
T1-weighted images are included and have been skull-stripped to protect subject anonymity. -
Demographics:
Subject-level demographic information, including group identifiers, is available indemographics.csv.
This organization makes the dataset straightforward to use in custom diffusion pipelines or for conversion into other diffusion MRI formats.
Scientific Context
Please refer to the following paper for a detailed description of the study population and scientific background:
Nielsen RB, Parbo P, Ismail R, Dalby RB,
Tietze A, Brændgaard H, Gottrup H,
Brooks DJ, Østergaard L and Eskildsen SF (2025)
Diffusion kurtosis imaging detects cortical microstructural alterations in amyloid-positive MCI patients.
Front. Dement. 4:1725754.
doi: 10.3389/frdem.2025.1725754
Article link:
https://www.frontiersin.org/journals/dementia/articles/10.3389/frdem.2025.1725754/abstract
Suggested Uses
This dataset can be used for:
- Diffusion kurtosis model fitting
- Comparison of DKI and conventional DTI metrics
- Studies of cortical microstructural alterations in MCI
- Biomarker development for early cognitive impairment
- Method development and validation for compact clinical diffusion datasets
- Multimodal analyses combining DKI and structural MRI
License
This dataset is distributed under the:
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International Public License (CC BY-NC-SA 4.0)
- Attribution required
- Non-commercial use only
- Share alike: derivative works must use the same license
Funding
- DFF-4004-00305
Citation
Please cite both the dataset and the associated publication:
Dataset:
Eskildsen, S.
Diffusion kurtosis MRI dataset
https://doi.org/10.6084/m9.figshare.30850301
Associated paper:
Nielsen RB, Parbo P, Ismail R, Dalby RB, Tietze A, Brændgaard H, Gottrup H, Brooks DJ, Østergaard L and Eskildsen SF (2025)
Diffusion kurtosis imaging detects cortical microstructural alterations in amyloid-positive MCI patients.
Front. Dement. 4:1725754.
https://doi.org/10.3389/frdem.2025.1725754
Notes for This Repository
The data-others/dki-mci release may include:
- Harmonized file naming
- Preorganized diffusion inputs for downstream processing
- Optional DSI Studio derivatives (
*.sz,*.fz) - QC summaries where available
Users should consult the original dataset and publication for full methodological details and cohort description.
Alzheimer's Disease vs Bipolar Disorder vs Healthy Control MRI Data and Processed Results
This dataset contains structural and diffusion MRI data together with derived FA, TBSS, and VBM results for patients diagnosed with Alzheimer’s Disease (AD), Bipolar Disorder (BD), and healthy controls (HC).
It includes corresponding clinical and biomarker information organized in structured .csv files, supporting both neuroimaging and clinical correlation studies.
The dataset has been used in multiple peer-reviewed publications investigating white matter integrity, biomarker correlation, and multivariate diagnostic modeling of neurodegenerative and psychiatric disorders.
License
Creative Commons Attribution 4.0 International (CC BY 4.0)
Citation
Besga, A., Graña, M., & Chyzhyk, D. (2020).
Alzheimer’s Disease versus Bipolar Disorder versus Healthy Control MRI Data and Processed Results [Data set]. Zenodo.
https://doi.org/10.5281/zenodo.3935636
Source
https://doi.org/10.5281/zenodo.3935636
Contact: ariadna.besga@ehu.eus
Institutions: University of the Basque Country (UPV/EHU), University of Navarra, University of the Basque Country
Funding: European Commission — CybSPEED: Cyber-Physical Systems for PEdagogical Rehabilitation in Special Education (Grant No. 777720)
Dataset Information
| Category | Details |
|---|---|
| Subjects | Patients diagnosed with Alzheimer’s Disease (EA), Bipolar Disorder (TB), and healthy controls (CRL) |
| Study Type | Structural and diffusion MRI with derived FA, TBSS, and VBM analyses |
| File Format | NIfTI (.nii/.nii.gz) for imaging, CSV for clinical data |
| Tools Used | FSL (DTI, TBSS), SPM (VBM), MATLAB, Python, R |
| Diagnostic Codes | crl = control, tb = bipolar disorder, ea = Alzheimer’s disease |
| Anonymization | All subjects identified by numerical random keys |
| Registration | Nonlinear alignment to MNI space using FSL |
| Publication Use | Multiple neuroscience and diagnostic modeling studies |
Clinical Data
The Clinical_data folder contains .csv files readable in Python, R, MATLAB, or any spreadsheet software.
Each file corresponds to a specific biomarker.
Key files include:
clinical_data_id_age_gender.csv: anonymized ID, diagnostic key, age, and gender.clinical_data_corrected.csv: deprecated, can be ignored.
Diagnostic key:
crl= Healthy controltb= Bipolar disorderea= Alzheimer’s disease
Publications Using This Dataset
- Graña et al. (2011) — Computer Aided Diagnosis system for Alzheimer’s Disease using DTI features, Neuroscience Letters, 502(3):225–229.
- Besga et al. (2012) — Discovering Alzheimer’s disease and bipolar disorder white matter effects using DTI, Neuroscience Letters, 520(1):71–76.
- Termenon et al. (2013) — Lattice ICA feature selection on DWI for Alzheimer’s classification, Neurocomputing, 114:132–141.
- Besga et al. (2015) — Discrimination between AD and late-onset BD using multivariate analysis, Frontiers in Aging Neuroscience, 7:231.
- Besga-Basterra et al. (2016) — Eigenanatomy on FA imaging differentiates AD and BD, Current Alzheimer Research, 13(5):557–565.
- Besga et al. (2017) — White matter tract integrity and inflammation in AD vs BD, Frontiers in Aging Neuroscience, 9:179.
Purpose
This dataset supports research in neurodegenerative and affective disorder differentiation, enabling:
- Quantitative analysis of white matter microstructure (FA, TBSS).
- Morphometric evaluation via SPM-based VBM.
- Correlation between MRI-derived features and clinical biomarkers.
- Machine learning model training for computer-aided diagnosis (CAD) of AD vs BD.
Keywords
MRI • Diffusion MRI • FA • TBSS • VBM • Alzheimer’s Disease • Bipolar Disorder • Healthy Control • FSL • SPM • Neurodegeneration • White Matter Integrity • Biomarkers
High‑Quality Diffusion‑Weighted Imaging of Parkinson’s Disease
A curated dataset and analysis pipelines for a cross‑sectional Parkinson’s disease (PD) study, designed to support reproducible research in diffusion MRI.
📄 License
This work is licensed under Creative Commons Attribution‑ShareAlike (CC BY‑SA).
- NITRC Image Repository: parktdi
📋 Overview
This project contains data and analysis pipelines for a set of 53 subjects in a cross‑sectional PD study:
- 27 PD patients
- 26 age, sex, and education‑matched controls
The diffusion‑weighted images (DWI) were acquired with:
- 120 unique gradient directions
- b = 1000 and b = 2500 s/mm²
- Isotropic 2.4 mm³ voxels
- Twice‑refocused spin‑echo sequence to minimize eddy‑current distortions
3T Diffusion MRI Inter-Site Reproducibility Dataset for Cerebral Small Vessel Disease
This dataset provides multi-site diffusion MRI data from 10 patients diagnosed with the genetically defined small vessel disease CADASIL, scanned on two different 3 T Siemens MRI scanners (Magnetom Prisma and Magnetom Skyra) within 24 hours.
It enables evaluation of inter-scanner reproducibility of diffusion metrics in cerebral small vessel disease (SVD) and supports harmonization studies for multi-center neuroimaging trials.
The dataset was used in the publication:
Konieczny & Dewenter et al., Neurology, 2020 — https://doi.org/10.1212/WNL.0000000000011213
License
Creative Commons Attribution – NonCommercial 4.0 International (CC BY-NC 4.0)
Citation
Dewenter, A., Gesierich, B., & Duering, M. (2020).
3T diffusion MRI inter-site reproducibility dataset for cerebral small vessel disease [Data set]. Zenodo.
https://doi.org/10.5281/zenodo.16925507
Source
https://doi.org/10.5281/zenodo.16925507
Contact: marco.duering@med.uni-muenchen.de
Institution: Institute for Stroke and Dementia Research (ISD), LMU Munich, Germany
Associated publication: Neurology, 96(5), e698–e708 (2020)
Dataset Information
| Category | Details |
|---|---|
| Subjects | 10 patients with CADASIL (genetically confirmed or via skin biopsy) |
| Age (median [IQR]) | 55.5 years (13.3) |
| Sex | 5 female (50 %) |
| Hypertension / Hypercholesterolemia | 3 / 5 patients |
| WMH volume [% ICV] median (IQR) | 7.67 (2.62) |
| Lacune count median (IQR) | 3 (7.75) |
| Brain volume [% ICV] median (IQR) | 75.7 (7.03) |
| Scanner Types | Siemens 3 T Magnetom Prisma and Skyra |
| Scan Interval | < 24 hours |
| Protocol | Matched b-values, gradient directions, and resolution between scanners |
| BIDS-Compliance | Data organized per subject and session (/sub-XX/ses-prisma, /ses-skyra) |
| Preprocessing Tools | dcm2niix, MRtrix (dwidenoise & mrdegibbs), FSL (TOPUP & EDDY) |
| Anonymization | Fully de-identified and restricted to diffusion MRI only |
MRI Acquisition Protocol
| Parameter | Magnetom Skyra | Magnetom Prisma |
|---|---|---|
| Coil | 64-channel head/neck | 64-channel head/neck |
| TR (ms) | 3800 | 3200 |
| TE (ms) | 104.8 | 74 |
| Resolution (mm³) | 2×2×2 | 2×2×2 |
| b-values (s/mm²) | 1000 / 2000 | 1000 / 2000 |
| Directions (per b) | 30 / 60 | 30 / 60 |
| b = 0 images | 10 | 10 |
| Multi-band factor | 3 | 3 |
| Acceleration factor | 2 | 2 |
Both scanners were located in separate hospital buildings with independent infrastructure, establishing a true inter-site condition despite institutional proximity.
Data Structure and Preprocessing
The dataset follows the BIDS organization scheme:
/sub-01
/ses-prisma
/dwi_raw
/dwi_preprocessed
/ses-skyra
/dwi_raw
/dwi_preprocessed
- Raw data converted from DICOM via dcm2niix
- Preprocessed data includes denoising (MRtrix
dwidenoise), Gibbs correction (mrdegibbs), and motion/eddy distortion correction (FSLTOPUP,EDDY).
Purpose
This dataset serves as a benchmark for assessing inter-scanner reproducibility and harmonization of diffusion MRI measures across 3 T sites.
It is particularly relevant for researchers working on:
- Cross-site calibration of diffusion metrics in small vessel disease
- Methodological validation of preprocessing and harmonization pipelines
- Clinical reproducibility of DTI/DKI biomarkers in multicenter trials
Keywords
Diffusion MRI • DTI • CADASIL • Small Vessel Disease • Inter-site Reproducibility • Siemens Prisma • Siemens Skyra • BIDS • FSL • MRtrix • Neurology 2020