4.7 Article

Comparison of spiral-in/out and spiral-out BOLD fMRI at 1.5 and 3T

Journal

NEUROIMAGE
Volume 21, Issue 1, Pages 291-301

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2003.09.017

Keywords

spiral-in/out; BOLD; fMPI

Funding

  1. NCRR NIH HHS [P41 RR009784, RR09784] Funding Source: Medline
  2. NIMH NIH HHS [R01 MH061426, F31 MH063576, MH63576, F32 MH081583, MH61426] Funding Source: Medline
  3. NATIONAL CENTER FOR RESEARCH RESOURCES [P41RR009784] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE OF MENTAL HEALTH [F31MH063576, R01MH061426] Funding Source: NIH RePORTER

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Spiral-in/out functional magnetic resonance imaging (fMRI) methods acquire one image before the echo time (TE) and a second image after TE during each scan. Weighted combination of the two images provides a time series with reduced susceptibility dropout in frontal and medial temporal regions as well as increased signal-to-noise ratio (SNR) in regions of uniform cortex. In this study, task activation with the spiral-in/out method was compared to that with conventional spiral-out acquisitions at two field strengths (1.5 and 3.0 T) using episodic memory encoding, verbal working memory, and affective processing tasks in eight human volunteers. With the conventional spiral-out sequence, greater signal dropout is observed in lateral and medial prefrontal, amygdalar, and medial temporal regions at 3 T relative to 1.5 T, whereas such dropout at 3 T is reduced or mitigated with the spiral-in/out method. Similarly, activation volumes for frontal, amygdalar. and medial temporal regions are reduced for spiral-out acquisitions relative to spiral-in/out, and this difference is more apparent at 3 T than at 1.5 T. In addition, significant regionally specific increases in Z scores are obtained with the spiral-in/out sequence relative to spiral-out acquisitions at both field strengths. It is concluded the spiral-in/out sequence may provide significant advantages over conventional spiral methods, especially at 3 T. (C) 2003 Elsevier Inc. All rights reserved.

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