Quantitative liver ADC measurements using diffusion-weighted MRI at 3 Tesla: evaluation of reproducibility and perfusion dependence using different techniques for respiratory compensation
Object Diffusion weighted imaging (DWI) of the liver suffers from low signal to noise making 3 Tesla (3 T) an attractive option, but 3 T data is scarce. It was the aim to study the influence of different b values and respiratory compensation methods (RCM) on the apparent diffusion coefficient (ADC)...
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Veröffentlicht in: | Magma (New York, N.Y.) N.Y.), 2013-10, Vol.26 (5), p.431-442 |
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Sprache: | eng |
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Zusammenfassung: | Object
Diffusion weighted imaging (DWI) of the liver suffers from low signal to noise making 3 Tesla (3 T) an attractive option, but 3 T data is scarce. It was the aim to study the influence of different
b
values and respiratory compensation methods (RCM) on the apparent diffusion coefficient (ADC) level and on ADC reproducibility at 3 T.
Materials and methods
Ten healthy volunteers and 12 patients with malignant liver lesions underwent repeated (2–22 days) breathhold, free-breathing and respiratory triggered DWI at 3 T using
b
values between 0 and 1,000 s/mm
2
.
Results
The ADCs changed up to 150 % in healthy livers and up to 48 % in malignant lesions depending on
b
value combinations. Best ADC reproducibility in healthy livers were obtained with respiratory triggering (95 % limits of agreement: ±0.12) and free-breathing (±0.14). In malignant lesions equivalent reproducibility was obtained with less RCM dependence. The use of a lower maximum
b
value (
b
= 500) decreased reproducibility (±0.14 to ±0.32) in both normal liver and malignant lesions.
Conclusion
Large differences in absolute ADC values and reproducibility caused by varying combinations of clinically realistic
b
values were demonstrated. Different RCMs caused smaller differences. Lowering maximum
b
value to 500 increased limits of agreement up to a factor of two. Serial ADC changes larger than approximately 15 % can be detected confidently on an individual basis in both malignant lesions and normal liver parenchyma at 3 T using appropriate
b
values and respiratory compensation. |
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ISSN: | 0968-5243 1352-8661 |
DOI: | 10.1007/s10334-013-0375-6 |