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TRADITIONAL POSTER - ismrm

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Poster Sessions<br />

2944. Sensitivity of MRI Resonance Frequency to the Orientation of Brain Tissue Microstructure<br />

Jongho Lee 1 , Karin Shmueli 1 , Masaki Fukunaga 1 , Peter van Gelderen 1 , Hellmut Merkle 1 , Afonso C. Silva 2 ,<br />

Jeff H. Duyn 1<br />

1 Advanced MRI/LFMI/NINDS, National Institutes of Health, Bethesda, MD, United States; 2 CMU/LFMI/NINDS, National Institutes<br />

of Health, Bethesda, MD, United States<br />

Here we demonstrate microstructural orientation affects the MRI resonance frequency. The experiment was designed to avoid macroscopic susceptibility<br />

effect to identify true microstructural effect. We suggest an origin related to anisotropic susceptibility.<br />

Relaxometry<br />

Hall B Monday 14:00-16:00<br />

2945. Wide-Range T1 Mapping Using Two Variable Flip Angle Acquisitions<br />

Rahul Sarkar 1 , Alan R. Moody 1,2 , James Q. Zhan 2 , General Leung 1,2<br />

1 Medical Biophysics, University of Toronto, Toronto, Ontario, Canada; 2 Medical Imaging, Sunnybrook Health Sciences Centre,<br />

Toronto, Ontario, Canada<br />

Variable flip angle (VFA) methods using two optimized flip angles have become popular for in-vivo T1 mapping within a limited range of a specific T1 of<br />

interest. The range limitation in this approach is generally due to bias against long T1s in the signal-dynamic range product used for flip angle optimization.<br />

This study presents a new strategy for flip angle pair selection that mitigates this bias to provide highly uniform accuracy and precision across the biological<br />

T1 range. In using only two flip angle acquisitions, this method represents a rapid approach to wide-range VFA T1 mapping.<br />

2946. Fast T 1 Mapping of Mouse Brain at 7 T with Time-Optimized Partial Inversion Recovery Utilizing a<br />

Surface Coil<br />

Naoharu Kobayashi 1 , Hironaka Igarashi 1 , Tsutomu Nakada 1<br />

1 Center for Integrated Human Brain Science, Brain Research Institute, University of Niigata, Niigata, Japan<br />

We present a new method for measuring a longitudinal relaxation time, T 1 , for a surface coil application utilizing adiabatic saturation pulses, referred to here<br />

as time-optimized partial inversion recovery (TOPIR). The recovery delays before and after the inversion pulse were optimized to sample data points such<br />

that the total sequence time was minimized under a specified dynamic range of the recovery curve. Accuracy of the method was validated by comparing the<br />

values obtained utilizing conventional inversion recovery sequence. The method enabled a two dimensional T 1 mapping of a mouse brain using a 6 point<br />

recovery curve in 20–36 s.<br />

2947. The Effect of Heart Rate in Look-Locker Cardiac T 1 Mapping<br />

Glenn S. Slavin 1 , Ting Song 1 , Jeffrey A. Stainsby 2<br />

1 Applied Science Laboratory, GE Healthcare, Bethesda, MD, United States; 2 Applied Science Laboratory, GE Healthcare, Toronto,<br />

ON, Canada<br />

Because inversion times in cardiac Look-Locker acquisitions are a function of heart rate, T1 measurements can be incorrect. Pulse sequence modifications to<br />

account for heart rate variability and its effect on the magnetization recovery curve can significantly improve T1 accuracy.<br />

2948. Demonstrating the Influence of Magnetisation Transfer on Putative T 1 Relaxation Times: A Simulation<br />

Study<br />

Miriam Rabea Kubach 1 , Kaveh Vahedipour 2 , Ana Maria Oros-Peusquens 2 , Tony Stoecker 2 , N. Jon Shah 2,3<br />

1 Institute of Neuroscience and Medicine , Forschungszentrum Juelich, Juelich, Germany; 2 Institute of Neuroscience and Medicine,<br />

Forschungszentrum Juelich, Juelich, Germany; 3 Faculty of Medicine, Department of Neurology, , RWTH Aachen University, JARA,,<br />

Aachen, Germany<br />

T1 is an MRI parameter very sensitive to pathological changes. Proper T1-mapping is therefore vital for many MRI applications, but the variability of T1<br />

values within different methods is larger than within a group of volunteers measured with the same method. The accuracy of the T1 determination is affected<br />

by a number of rectifiable parameters but also influenced by MT in ways, which are strongly method-dependent and usually not quantified. We present<br />

numerical simulations, based on an existing software package JEMRIS, which allow one to simulate MR sequences considering MT effects. We investigate<br />

changes in the T1 relaxation of the observable water component due to the presence of and exchange with a bound proton pool. A simple pulse-acquire<br />

sequence is used for simulations, which can be the elementary building block of more realistic MR imaging sequences.<br />

2949. Fast T1/B1 Mapping Using Multiple Dual TR RF-Spoiled Steady-State Gradient-Echo Sequences<br />

Tobias Voigt 1 , Stefanie Remmele 2 , Ulrich Katscher 2 , Olaf Doessel 1<br />

1 Institute of Biomedical Engineering, University of Karlsruhe, Karlsruhe, Germany; 2 Philips Research Europe, Hamburg, Germany<br />

Efficient and accurate baseline T1 and B1 quantification is a pre-requisite for standardized and clinical Dynamic Contrast-Enhanced MRI (DCE-MRI). This<br />

study investigates a new approach called “Multiple TR B1/T1 Mapping” (MTM), capable of fast, simultaneous B1 and T1 mapping. In this work, MTM is<br />

analysed with respect to its T1 mapping performance in comparison with an inversion recovery reference sequence and in due consideration of the limited<br />

time allowed in a clinical set-up. In calibrated phantom measurements, MTM T1 mapping was found to be more accurate than IR-TSE, inter alia due to its<br />

intrinsic B1 correction mechanism.

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