This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.* This project was recently funded under grant R21-EB005690 to Nan-kuei Chen.* Grant relinquished from BWH to Duke University as of November 1, 2007. SummaryThe goal of this project is to improve the quality and spatial accuracy of echo-planar imaging (EPI), so that accurate quantitative information can be derived from EPI based medical research and clinical diagnosis. EPI is one of the fastest MR imaging techniques, and has been popularly applied to various dynamic studies that require high temporal-resolution, such as functional MRI (fMRI), contrast-enhanced imaging, and MR based interventional procedures. However, EPI data quality is usually degraded by various artifacts, such as geometric distortions and susceptibility signal loss. Furthermore, the sensitivity of EPI to susceptibility field nhomogeneities makes it less reliable in EPI based longitudinal studies. Several techniques have been previously reported for EPI quality improvement and artifact reduction. However, most previously reported EPI artifact reduction methods require time-consuming field mapping scans, and therefore may not always be practical (e.g. for clinical scans and EPI based interventional MRI procedures). Here we propose to use a novel k-space energy spectrum analysis to quantify (1) the k-space energy distribution, (2) susceptibility field gradients, (3) the spatially-dependent echo time values, and (4) artifact levels directly from the acquired EPI data, without the need of additional field mapping procedure or pulse sequence modification. Various EPI artifacts (e.g. distortions and Gibb's ripple artifact) can be effectively removed using the proposed approach. Furthermore, the developed k-space energy spectrum analysis will be applied to design an optimal acquisition strategy for phase-encoded 3D parallel EPI, with an improved signal-to-noise ratio and reduced motion related artifact. We also plan to apply the proposed methods to re-analyze the previously acquired fMRI data, and retrospectively improve the longitudinal reproducibility of grouped activation. The methods developed in the proposed project will be made available to MRI community so that other research groups may use the developed methods to improve their future EPI based quantitative studies or to retrospectively improve the EPI data that were previously obtained.[edit]Benefits to NCIGT * The KESA method can be applied to provide robust temperature maps using EPII through reliable phase unwrapping procedure to effectively eliminate the phase wraparounds in dynamic temperature mapping. Based on our k-space energy spectrum analysis algorithm (R21 project), a new phase mapping and unwrapping method is being designed. The MRI based temperature mapping will have a better tolerance to subject movement and susceptibility effect when the new reliable phase unwrapping procedure is included. Thus, this project supports our work in the development of new temperature mapping methods. * Field maps using the KESA method can be used for distortion correction in EPI-base fMRI and DTI. Thus this work supports our efforts in the Neurosurgery Core. Benefits to the ProjectThe IGT resource provides an essential support to the R21 project. The programming environment for development of the sequence is maintained (in part) through support from the imaging core of the resource. In addition, a training fellow attached to the IGT resource, Ming-Long Wu, is participating in the experimental work of the R21 project.[edit]Statement of the Collaboration in the U41 Grant ApplicationThis R21 project was not included in original grant application because it has been funded since then.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Cooperative Agreements (U41)
Project #
5U41RR019703-04
Application #
7719666
Study Section
Special Emphasis Panel (ZRG1-SBIB-L (40))
Project Start
2008-08-01
Project End
2009-07-31
Budget Start
2008-08-01
Budget End
2009-07-31
Support Year
4
Fiscal Year
2008
Total Cost
$28,171
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
030811269
City
Boston
State
MA
Country
United States
Zip Code
02115
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