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Abstract #5423

Fetal T1 mapping using multi-inversion EPI at 3T

Borjan Gagoski1,2, Daniel Joseph Park3, Ville Renvall3,4, Esra Abaci-Turk1,5, Elfar Adalsteinsson6,7, Thomas Witzel2,3, Lawrence L. Wald3,8, Patricia Ellen Grant1,5, and Jonathan Polimeni2,3

1Fetal Neonatal Neuroimaging and Developmental Science Center, Boston Children's Hospital, Boston, MA, United States, 2Department of Radiology, Harvard Medical School, Boston, MA, United States, 3Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Charlestown, MA, United States, 4Department of Neuroscience and Biomedical Engineering, Aalto University School of Science, Espoo, Finland, 5Department of Newborn Medicine, Harvard Medical School, Boston, MA, United States, 6Department of Electrical Engineering and Computer Science, Massachusetts Institute of Technology, Cambridge, MA, United States, 7Harvard-MIT Health Sciences and Technology, Institute of Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA, United States, 8Harvard-MIT Division of Health Sciences and Technology, Massachusetts Institute of Technology, Cambridge, MA, United States

T1 mapping of the fetal brain is hindered by substantial, frequent, and random fetal motion, making many current quantitative techniques impractical in the fetus. We have applied to the fetal brain (and adult brain for validation purposes) a recently introduced T1 mapping technique based on EPI readout that is preceded by a non-selective inversion pulse, and where the order of the acquired slices is permuted from one inversion recovery to the next, allowing efficient, high temporal sampling of the T1 relaxation curve. We believe that this method is capable of providing accurate T1 maps of the fetal brain.

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