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Development of a Double Echo-Shifted QUTE for quantification of T2* relaxation time at Ultra-High Field MRI.
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Motivation: T2* relaxation time is typically assessed using a multi-echo GRE sequence. However, the accurate quantification of slow-relaxing water pools, such as CSF, necessitates an extended scan time in comparison to that required for the quantification of brain tissue. Goal(s): We present a new sequence (DES-QUTE), which is capable of acquiring three bunches of echoes corresponding to short, intermediate, and long TEs without a significant increase in the scan time. Approach: The proposed sequence integrates QUTE with an improved echo-shifting technique. Results: The DES-QUTE demonstrated accurate and precise T2* quantification at ultra-high field MRI, while providing a potential for simultaneous quantification of diffusion coefficients. Impact: The proposed sequence offers an opportunity to sample different ranges of TE images and quantify both T2* and D information without a significant increase in scan time. This method is expected to make significant contributions to the study of neurofluids.
Title: Development of a Double Echo-Shifted QUTE for quantification of T2* relaxation time at Ultra-High Field MRI.
Description:
Motivation: T2* relaxation time is typically assessed using a multi-echo GRE sequence.
However, the accurate quantification of slow-relaxing water pools, such as CSF, necessitates an extended scan time in comparison to that required for the quantification of brain tissue.
Goal(s): We present a new sequence (DES-QUTE), which is capable of acquiring three bunches of echoes corresponding to short, intermediate, and long TEs without a significant increase in the scan time.
Approach: The proposed sequence integrates QUTE with an improved echo-shifting technique.
Results: The DES-QUTE demonstrated accurate and precise T2* quantification at ultra-high field MRI, while providing a potential for simultaneous quantification of diffusion coefficients.
Impact: The proposed sequence offers an opportunity to sample different ranges of TE images and quantify both T2* and D information without a significant increase in scan time.
This method is expected to make significant contributions to the study of neurofluids.
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