Jana Hutter1
1King's College London, United Kingdom
Synopsis
This talk will focus on the recent developments combining diffusion MRI with relaxometry. It will first give details on the parameters and choices available on the acquisition side. Next, possible analysis techniques will be presented and finally recent results detailing possible applications will be discussed.
Target Audience
Basic scientists and clinical scientists interested in microstructural
information, specifically in gaining an understanding how diffusion MRI and
relaxometry can be combined to yield novel insightsObjectives/Outcomes
- Understanding the intrinsic influence of
acquisition parameters on diffusion data
- Learn about ways to achieve combined diffusion-relaxometry
acquisition
- Discuss analysis methods dedicated to joint
diffusion-relaxometry data
- Learn about examples of applications where
diffusion-relaxometry yields novel insights
Purpose
Multi-parametric quantitative MRI techniques combining diffusion MRI and
relaxometry have recently gained significant interest due to their ability to
produce eloquent data allowing novel insights into the composition of
biological tissue in-vivo: While relaxometry accesses chemical properties,
diffusion MRI targets mechanical and geometrical properties of the tissue
microstructure. Their combination has great potential to characterize
biological tissue in ever more detail. The thus achieved window into physiology
offers a multitude of applications both for research and for clinical settings.
Diffusion MRI signal does not ever originate only from the targeted
microstructure, but also contains effects of tissue properties due to the
chosen sequence parameters (e.g. echo time TE, repetition time TR, flip angle
FA). Ignoring relaxometry effects thus risks to misinterpret signal variations
whilst including relaxometry effects in signal equations and models allows
potentially to disentangle the effects of T1/T2 weighting and diffusion
properties.Methods/Results
In this lecture both the intrinsic influence and possible consequences for
quantitative diffusion analysis as well the opportunities offered by joint
diffusion-relaxometry sampling will be discussed.
- Basic diffusion acquisition using single-shot EPI
including the discussion of all relevant acquisition parameters
- Novel combined acquisition techniques including
relevant parameter scheme design
- Analysis
techniques exploiting multi-dimensional diffusion-relaxometry data
Examples of multi-dimensional diffusion-relaxometry applications (brain, prostate,
placenta, kidney) will be given.
Discussion/Conclusion
An outlook will be given on possible further developments and how relevance
for clinical practise can be further increasedAcknowledgements
No acknowledgement found.References
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