Related Experiment Video
Updated: Sep 16, 2025

Registered Bioimaging of Nanomaterials for Diagnostic and Therapeutic Monitoring
Published on: December 9, 2010
Simultaneous liver T1, T2, and ADC MR fingerprinting using optimized motion-compensated diffusion preparations: An
C Velasco1, C Castillo-Passi1,2,3, N Chaher1
1School of Biomedical Engineering and Imaging Sciences, King's College London, London, UK.
This study introduces a new MR fingerprinting method for fast, simultaneous liver tissue T1, T2, and ADC mapping. The technique enables comprehensive hepatic disease evaluation in a single breath-hold scan.
Area of Science:
- Magnetic Resonance Imaging
- Medical Physics
- Biomedical Engineering
Background:
- Accurate quantification of liver tissue properties is crucial for diagnosing and staging hepatic diseases.
- Conventional multiparametric mapping techniques often require multiple scans, increasing acquisition time and potential for patient motion.
- MR fingerprinting offers a promising approach for rapid tissue characterization.
Purpose of the Study:
- To develop and validate a novel MR fingerprinting (MRF) sequence for simultaneous quantification of T1, T2, and apparent diffusion coefficient (ADC) in liver tissue.
- To achieve this quantification within a single, short, breath-held scan using optimized motion-compensated diffusion preparations.
- To enable comprehensive, co-registered multiparametric imaging for improved liver disease evaluation.
Main Methods:
- A radial spoiled gradient echo acquisition sequence was designed with integrated T1, T2, and ADC encoding modules.
- Motion compensation strategies, including breath-holding, peripheral pulse triggering, and optimized diffusion preparation, were employed to mitigate signal voids and artifacts.
- Phantom experiments validated accuracy, followed by in vivo evaluation in healthy subjects against conventional mapping and repeatability assessments.
Main Results:
- The developed MRF sequence demonstrated high accuracy and good correlation (r² > 0.9) with reference measurements in phantoms.
- In vivo results showed good agreement with conventional mapping techniques, with no significant bias.
- Repeatability assessments confirmed low interscan coefficients of variation and high intraclass correlation coefficients (> 0.9).
Conclusions:
- A novel MR fingerprinting sequence enables simultaneous T1, T2, and ADC quantification of liver tissue in approximately 16 seconds.
- This approach facilitates comprehensive, co-registered multiparametric imaging for hepatic disease evaluation.
- Further investigation in patients with diffuse liver disease is warranted to assess its potential for tissue characterization and tumor staging.
More Related Videos
09:59A Magnetic Resonance Imaging Protocol for Stroke Onset Time Estimation in Permanent Cerebral Ischemia
Published on: September 16, 2017
15:48Tracking the Mammary Architectural Features and Detecting Breast Cancer with Magnetic Resonance Diffusion Tensor Imaging
Published on: December 15, 2014