4.7 Article

A novel technique for modeling susceptibility-based contrast mechanisms for arbitrary microvascular geometries:: The finite perturber method

期刊

NEUROIMAGE
卷 40, 期 3, 页码 1130-1143

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2008.01.022

关键词

dynamic susceptibility; contrast; arbitrary geometry; microvasculature; tumor angiogenesis; BOLD fMRI

资金

  1. NCI NIH HHS [P50 CA103175, R01CA82500-01A1, R01 CA082500-03, R01 CA082500-05, R01 CA082500, P50CA103175, R01 CA082500-04, R01 CA082500-06, R01 CA082500-07, R01 CA082500-02, R01 CA082500-08] Funding Source: Medline
  2. NCRR NIH HHS [M01 RR000058-455105, M01 RR000058-440534, M01 RR000058, M01 RR000058-430534] Funding Source: Medline

向作者/读者索取更多资源

Recently, we demonstrated that vessel geometry is a significant determinant of susceptibility-induced contrast in MRI. This is especially relevant for susceptibility-contrast enhanced MRI of tumors with their characteristically abnormal vessel morphology. In order to better understand the biophysics of this contrast mechanism, it is of interest to model how various factors, including microvessel morphology contribute to the measured MR signal, and was the primary motivation for developing a novel computer modeling approach called the Finite Perturber Method (FPM). The FPM circumvents the limitations of traditional fixed-geometry approaches, and enables us to study susceptibility-induced contrast arising from arbitrary microvascular morphologies in 3D, such as those typically observed with brain tumor angiogenesis. Here we describe this new modeling methodology and some of its applications. The excellent agreement of the FPM with theory and the extant susceptibility modeling data, coupled with its computational efficiency demonstrates its potential to transform our understanding of the factors that engender susceptibility contrast in MRI. (C) 2008 Elsevier Inc. All rights reserved.

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