論文

査読有り
2011年

Acquisition Parameters for Diffusion Tensor Imaging to Emphasize Fractional Anisotropy: Phantom Study

MAGNETIC RESONANCE IN MEDICAL SCIENCES
  • Takenori Oida
  • ,
  • Shizue Nagahara
  • ,
  • Tetsuo Kobayashi

10
2
開始ページ
121
終了ページ
128
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.2463/mrms.10.121
出版者・発行元
JPN SOC MAGNETIC RESONANCE IN MEDICINE

Diffusion tensor imaging (DTI) is a magnetic resonance (MR) imaging technique that has attracted attention in recent years for applications such as nerve fiber tracking, neurography, and tumor detection. In DTI measurements, 2 motion-probing gradient (MPG) pulses are applied to evaluate water diffusion. In DTI for nerve fiber tracking, acquisition parameters, such as strength, duration, and separation of MPGs, influence the MR signal.
In this study, we set acquisition parameters in DTI to emphasize fractional anisotropy to clarify the direction of nerve fibers. We performed Monte Carlo simulations of restricted diffusion in a cylinder model and phantom measurements with capillary plates to examine the relationship between the acquisition parameters in DTI and the size of restricted structures, particularly their diameter and length, which we will refer to as "compartment size."
We confirmed that normalized signal intensities in DTI measurements depend on diffusion time, which, in turn, depends on the separation and duration of the MPG, and they decrease with increase in compartment size. Furthermore, our simulation and phantom results suggest that use of a longer diffusion time effectively emphasizes fractional anisotropy to clarify the direction of nerve fibers.

リンク情報
DOI
https://doi.org/10.2463/mrms.10.121
CiNii Articles
http://ci.nii.ac.jp/naid/10029698341
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/21720114
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000292073100007&DestApp=WOS_CPL
ID情報
  • DOI : 10.2463/mrms.10.121
  • ISSN : 1347-3182
  • CiNii Articles ID : 10029698341
  • PubMed ID : 21720114
  • Web of Science ID : WOS:000292073100007

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