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Abstract #4943

Readout Duration-dependent Bias on R2* Mapping and Quantitative Susceptibility Mapping Using 3D Radial and Cones Acquisitions at 3.0T

Shihan Qiu1, Timothy J. Colgan2, Ante Zhu2,3, Kevin M. Johnson2,4, Scott B. Reeder2,3,4,5,6, and Diego Hernando2,4

1Biomedical Engineering, Tsinghua University, Beijing, China, 2Radiology, University of Wisconsin, Madison, WI, United States, 3Biomedical Engineering, University of Wisconsin, Madison, WI, United States, 4Medical Physics, University of Wisconsin, Madison, WI, United States, 5Medicine, University of Wisconsin, Madison, WI, United States, 6Emergency Medicine, University of Wisconsin, Madison, WI, United States

Ultra-short TE (UTE) R2* mapping and Quantitative Susceptibility Mapping (QSM) are emerging techniques for quantifying iron deposition in various organs, including the brain and liver. In tissues with short T2* values (high R2*), the fast signal decay-induced errors during the relatively long readout in typical UTE acquisitions, i.e., 3D radial and cones UTE, may confound R2* and susceptibility measurements. In this study, we characterized the readout duration effects on R2* and susceptibility estimation in 3D radial and cones UTE-acquisitions at 3.0T. Simulation and phantom studies showed bias in the estimated R2* and susceptibility when long readout durations were used.

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