Gadoxetate kinetics measured with MRI
Creators
Description
Database
This database collects signal-time curves measured through the various experiments of the liver workpackage of the TRISTAN consortium. The database is maintained by the open medical imaging biomarkers laboratory (miblab.org).
Subjects
Human healthy volunteers, patients and rats.
Background
The data are taken from a series of preclinical and clinical studies performed by the TRISTAN project, in the period 2018-2024. The aim of these studies was to test if the effect of drugs on uptake and excretory function of the liver can be measured reliably with dynamic gadoxetate-enhanced MRI. Combined these studies provide proof of concept for a new MRI-based biomarker to predict the risk of liver-mediated drug-drug interactions, and of drug-induced liver injury.
The data have been used to support a submission to the FDA's biomarker qualification program (details).
Format
All data are in dmr format - a folder with three csv files:
- data.csv: Data dictionary
- rois.csv: ROI curves
- pars.csv: Subject parameters
The data can be read and manipulated interactively with common applications such as excel, or programmatically with the python package pydmr.
Example usage
- Rats multiple dosing: https://dcmri.org/examples/liver/plot_tristan_mdosing.html
- Rat six test drugs: https://dcmri.org/examples/liver/plot_tristan6drugs.html
- Rat reproducibility: https://dcmri.org/examples/liver/plot_tristan_repro.html
- Healthy volunteers: https://dcmri.org/examples/liver/plot_tristan_volunteers_2scan.html
- Patients: https://dcmri.org/examples/liver/plot_tristan_patients.html
Version history
- v0.0.6
- Rat data separated out per study in line with the human data
- v0.0.5
- Removed non-kinetic data due to a miblab database restructure.
- v0.0.4
- Added covariates for LDS subjects
- v0.0.3
- Added results for all human data
- v0.0.2
- Removed duplicate human results and combined all controls without treatment in a single file
- Unique naming of subject ID's by adding a study acronym to the subject number: LDS for Leeds subjects, SHF for Sheffield subjects and GOT for Gothenburg subjects
- v0.0.1
- Combined various formats of previous studies in a coherent dmr format
Datasets
tristan_humans_healthy_rifampicin
The research question was to what extent rifampicin inhibits gadoxetate uptake rate from the extracellular space into the liver hepatocytes (khe, mL/min/100mL) and excretion rate from hepatocytes to bile (kbh, mL/100mL/min). 2 of the volunteers only had the baseline assessment, the other 8 volunteers completed the full study. The results showed consistent and strong inhibition of khe (95%) and kbh (40%) by rifampicin. This implies that rifampicin poses a risk of drug-drug interactions (DDI), meaning it can cause another drug to circulate in the body for far longer than expected, potentially causing harm or raising a need for dose adjustment.
- time_1: acquisition times of the first scan
- time_2: acquisition times of the second scan
- aorta_1: aorta signals in the first scan
- aorta_2: aorta signals in the second scan
- liver_1: liver signals in the first scan
- liver_2: liver signals in the second scan
- aorta_1_accept: valid aorta signals in the first scan
- aorta_2_accept: valid aorta signals in the second scan
- liver_1_accept: valid liver signals in the first scan
- liver_2_accept: valid liver signals in the second scan
- weight: subject weight in kg.
- dose_1: contrast agent doses of first scan in mL/kg.
- dose_2: contrast agent doses of second scan in mL/kg.
- rate: contrast agent injection rate in mL/sec.
- FA_1: Flip angle in degrees of the first scan
- FA_2: Flip angle in degrees of the second scan
- TR: repetition time in sec
- t0: baseline length
- T1_aorta_1: precontrast T1 of blood
- T1_aorta_2: T1 of blood after 1st dynamic
- T1_aorta_3: T1 of blood at the start of the 2nd scan
- T1_liver_1: precontrast T1 of the liver
- T1_liver_2: T1 of the liver after 1st dynamic
- T1_liver_3: T1 of the liver at the start of the 2nd scan
- liver_volume: liver volume in mL.
The data confirmed that patients had significantly reduced uptake and excretion function in the absence of rifampicin. Rifampicin administration improved their excretory function but had no effect on their uptake function.
- time: array of time points in sec
- spleen: array of spleen signals in arbitrary units
- liver: array of liver signals in arbitrary units.
- FA: Flip angle in degrees
- TR: repetition time in sec
- n0: number of precontrast acquisitions
- study: an integer identifying the substudy the scan was taken in
- subject: a study-specific identifier of the subject in the range 1-6.
- visit: either 1 (baseline) or 2 (drug or vehicle/saline).
- center: center wehere the study was performed, either E, G or D.
- field_strength: B0-field of scanner on whuch the study was performed
- substance: what was injected, eg. saline, vehicle or drug name.
- BAT: Bolus arrival time
- duration: duration on the injection in sec.
Files
tristan_humans_healthy_ciclosporin.dmr.zip
Files
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Additional details
Funding
Software
- Development Status
- Active