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Author Spotlight: Advancing Hepatic Fibrosis Diagnosis Using Magnetic Resonance Elastography and AI
Published on: July 21, 2023
Task-based optimization of flip angle for fibrosis detection in T1-weighted MRI of liver
Jonathan F Brand1, Lars R Furenlid2, Maria I Altbach3
1University of Arizona , College of Optical Sciences, 1630 East University Boulevard, Tucson, Arizona 85719, United States.
Insights
Magnetic resonance imaging (MRI) can detect hepatic fibrosis (HF) by analyzing liver texture. Optimizing MRI pulse sequences improves the accuracy of this non-invasive diagnostic method for chronic liver disease.
Area of Science:
- Medical Imaging
- Hepatology
- Biomedical Engineering
Background:
- Chronic liver disease is a global health concern, with hepatic fibrosis (HF) as a key indicator.
- Current HF diagnosis relies on liver biopsy, which has limitations like sampling errors and procedural risks.
- Pathological HF diagnosis involves identifying textural changes indicative of collagen deposition within liver lobules.
Purpose of the Study:
- To develop and validate a non-invasive method for detecting hepatic fibrosis using MRI.
- To optimize MRI pulse sequences for enhanced detection of HF-related textural changes.
- To train model observers for accurate HF detection based on MRI phantoms.
Main Methods:
- Utilized ex vivo formalin-fixed human liver samples as phantoms to mimic in vivo Gd-MRI textural contrast.
- Developed a local texture analysis algorithm applied to phantom MRI images.
- Trained model observers using phantom image analysis to detect HF, assessing performance with AUROC.
- Optimized MRI pulse sequences by varying flip angles to maximize AUROC for HF detection.
Main Results:
- A local texture analysis method was successfully developed and applied to MRI phantoms.
- Model observers trained on phantom data demonstrated the potential for detecting HF.
- Optimized MRI pulse sequences, determined by maximizing AUROC, enhance HF detection capabilities.
- The study established a correlation between MRI textural features and HF presence.
Conclusions:
- MRI-based texture analysis shows promise as a non-invasive tool for hepatic fibrosis detection.
- Optimized MRI pulse sequences can improve diagnostic accuracy for HF.
- This approach may offer a safer and more reliable alternative to liver biopsy for HF assessment.
Abstract:
Chronic liver disease is a worldwide health problem, and hepatic fibrosis (HF) is one of the hallmarks of the disease. The current reference standard for diagnosing HF is biopsy followed by pathologist examination; however, this is limited by sampling error and carries a risk of complications. Pathology diagnosis of HF is based on textural change in the liver as a lobular collagen network that develops within portal triads. The scale of collagen lobules is characteristically in the order of 1 to 5 mm, which approximates the resolution limit of in vivo gadolinium-enhanced magnetic resonance imaging in the delayed phase. We use MRI of formalin-fixed human ex vivo liver samples as phantoms that mimic the textural contrast of in vivo Gd-MRI. We have developed a local texture analysis that is applied to phantom images, and the results are used to train model observers to detect HF. The performance of the observer is assessed with the area-under-the-receiver-operator-characteristic curve (AUROC) as the figure-of-merit. To optimize the MRI pulse sequence, phantoms were scanned with multiple times at a range of flip angles. The flip angle that was associated with the highest AUROC was chosen as optimal for the task of detecting HF.
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