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Functional MRI at 3T using intermolecular double-quantum coherence (iDQC) with spin-echo (SE) acquisitions
Authors:T. Gu  S. D. Kennedy  Z. Chen  K. A. Schneider  J. Zhong
Affiliation:(1) Department of Imaging Sciences, University of Rochester, Rochester, NY 14642, USA;(2) Rochester Center for Brain Imaging, University of Rochester, Rochester, NY 14642, USA;(3) Department of Biochemistry and Biophysics, University of Rochester, Rochester, NY 14642, USA;(4) Department of Visual Science, University of Rochester, Rochester, NY 14642, USA;(5) Department of Imaging Sciences, School of Medicine and Dentistry, University of Rochester, Box 648, Elmwood Avenue, Rochester, NY 14642-8648, USA
Abstract:
Object To reinvestigate the dependence of the signal and contrast on sequence parameters and tissue relaxation times for intermolecular double-quantum coherence (iDQC) signals, and to explore the possibility to use a spin-echo (SE)-iDQC sequence for detecting activation signals at 3T. Materials and methods Brain activations were detected in five human volunteers in a visual simulation study using a SE-iDQC sequence, in addition to a GE-iDQC and a conventional single-quantum coherence (SQC) blood-oxygenation-level-dependent (BOLD) sequence. A brain phantom was also used for some quantitative measurements. Results By choosing an optimal echo time TE (~T2) and iDQC evolution time τ(~20 ms), robust brain activations were detected using the SE-iDQC sequence, in addition to the GE-iDQC and a conventional single-quantum coherence (SQC) BOLD sequence. A higher percentage signal change due to activation was observed for both the iDQC-based measurements in comparison to the conventional SQC acquisition. Conclusion Even though a phenomenological analysis consistent with the experimental results was provided, a detailed model is still needed for the contrast mechanism at microscopic level to guide potential applications of brain functional imaging based on the SE-iDQC.
Keywords:fMRI  Intermolecular double-quantum coherence (iDQC)  Distant dipolar field (DDF)  Spin echo (SE)
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