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Published on: May 31, 2024
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Automated Quality Evaluation Index for Arterial Spin Labeling Derived Cerebral Blood Flow Maps
Sudipto Dolui1, Ze Wang2, Ronald L Wolf1,3
1Department of Radiology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
Journal of Magnetic Resonance Imaging : JMRI
|February 24, 2024
Summary
A new automated quality evaluation index (QEI) for arterial spin labeling (ASL) cerebral blood flow (CBF) maps shows performance comparable to manual assessments. This automated QEI offers scalable quality control for ASL imaging.
Area of Science:
- Neuroimaging
- Medical Physics
- Radiology
Background:
- Arterial spin labeling (ASL) derived cerebral blood flow (CBF) maps can suffer from artifacts and noise, impacting image quality.
- Objective assessment of ASL CBF map quality is crucial for reliable clinical interpretation.
Purpose of the Study:
- To develop and validate an automated, objective quality evaluation index (QEI) for ASL CBF maps.
- To establish a scalable method for quality control in ASL neuroimaging.
Main Methods:
- Developed a QEI using 101 2D ASL CBF maps rated by neuroradiologists.
- Validated the QEI through cross-validation, correlation with CBF reproducibility, effect size analysis, and comparison with manual ratings and an existing automated metric.
- Utilized data from 221 adults, including patients with Alzheimer's disease, Parkinson's disease, and traumatic brain injury.
Main Results:
- The automated QEI demonstrated strong correlation with manual quality ratings (R=0.83 for 2D, R=0.86 for 3D ASL).
- QEI showed significant inverse correlation with CBF reproducibility (R=-0.74) and improved effect sizes when low-quality data was excluded.
- The developed QEI outperformed a previously existing automated quality metric.
Conclusions:
- The automated QEI provides a reliable and scalable method for quality control of ASL CBF maps.
- This automated approach achieves performance comparable to expert manual ratings.
- The QEI can enhance the consistency and accuracy of ASL-based neuroimaging analyses.

