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Patient respiratory-triggered quantitative T2 mapping in the pancreas
Naïk Vietti Violi1, Tom Hilbert1,2,3, Jessica A M Bastiaansen1
1Department of Radiology, University hospital (CHUV) and University of Lausanne (UNIL), Lausanne, Switzerland.
Accelerated T2 mapping at 3 Tesla is feasible for pancreas imaging, offering stable and reproducible quantitative T2 values. This technique shows promise for assessing diffuse pancreatic disease in patients.
Area of Science:
- Magnetic Resonance Imaging
- Quantitative Imaging
- Medical Physics
Background:
- Abdominal T2 mapping is limited by long acquisition times and motion sensitivity.
- Accelerated T2 mapping at 3 Tesla (3 T) may enable quantitative assessment of diffuse pancreatic disease during free-breathing.
Purpose of the Study:
- To evaluate the feasibility of respiratory-triggered quantitative T2 analysis in the pancreas.
- To correlate T2 values with patient demographics, pancreatic location, duct dilatation, and pathology.
Main Methods:
- A 10-fold accelerated multiecho-spin-echo sequence was used for T2 quantification at 3 T.
- Two radiologists delineated regions of interest in the pancreatic head, body, and tail.
- Interreader reliability and associations between T2 values and clinical/radiological data were assessed.
Main Results:
- The accelerated sequence was successfully performed in 88 adults with a mean acquisition time of 2:48 min.
- Low intersubject T2 value variability was observed across pancreatic regions (head: 60.2 ± 8.3 msec, body: 63.9 ± 11.5 msec, tail: 66.8 ± 16.4 msec).
- Good interreader agreement (ICC, 0.82) was achieved. T2 values significantly correlated with age, pancreatic location, main pancreatic duct dilatation, and diffuse pancreatic disease.
Conclusions:
- Accelerated T2 mapping at 3 T is feasible and reproducible for pancreas imaging, even with organ motion.
- T2 values in the pancreatic parenchyma are significantly influenced by demographic and clinical factors.
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