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Multi-system repeatability and reproducibility of apparent diffusion coefficient measurement using an ice-water
Dariya Malyarenko1, Craig J Galbán, Frank J Londy
1Department of Radiology, University of Michigan, Ann Arbor, Michigan, USA.
Journal of Magnetic Resonance Imaging : JMRI
|October 2, 2012
Summary
Standardizing diffusion weighted imaging (DWI) protocols improved the reproducibility of apparent diffusion coefficient (ADC) measurements across multiple centers. This quality control identified spatial ADC nonuniformity as a key error source in multi-site clinical trials.
Area of Science:
- Medical Imaging
- Biomarker Development
- Quantitative MRI
Background:
- Apparent diffusion coefficient (ADC) is a promising biomarker for multi-center clinical trials.
- Technical variability in ADC measurements can hinder multi-center study reliability.
- Standardized quality control procedures are essential for robust multi-center biomarker applications.
Purpose of the Study:
- To establish quantitative quality control (QC) procedures for multi-center ADC measurements.
- To evaluate and minimize technical variability in diffusion coefficient measurements.
- To ensure the reliable use of ADC as a biomarker in multi-center clinical trials.
Main Methods:
- A uniform diffusion weighted imaging (DWI) protocol was developed and distributed to 18 test sites.
- A temperature-controlled diffusion phantom was used for data acquisition across 35 MRI systems (1.5T and 3T).
- Data from ice water diffusion imaging at five b-values were centrally analyzed.
Main Results:
- Inter-scanner ADC variability was less than 2% at the bore center, with an error range of -2% to +5% from the literature value.
- Day-to-day and intra-exam repeatability were within 4.5% and 1%, respectively.
- Inter-site reproducibility was within 3% at the magnet isocenter, but off-center measurements revealed significant vendor- and system-specific spatial ADC nonuniformity bias (>10%), linked to gradient nonlinearity.
Conclusions:
- Standardization of DWI protocols significantly enhances the reproducibility of ADC measurements.
- Spatial ADC nonuniformity was identified as a critical source of error in multi-site studies.
- Implementing these QC procedures is crucial for reliable multi-center clinical trials using ADC.

