Two-component diffusion tenser MRI of isolated perfused hearts

被引:55
作者
Hsu, EW [1 ]
Buckley, DL
Bui, JD
Blackband, SJ
Forder, JR
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[2] Duke Univ, Med Ctr, Ctr Vivo Microscopy, Durham, NC USA
[3] Univ Florida, Dept Neurosci, Gainesville, FL 32610 USA
[4] Univ Florida, Dept Physiol, Gainesville, FL 32610 USA
[5] Univ Florida, Florida Brain Inst, Gainesville, FL USA
[6] Natl High Magnet Field Lab, Tallahassee, FL USA
关键词
biexponential decay; fiber orientation mapping; myocardial microstructure; compartmental analysis; anisotropic diffusion;
D O I
10.1002/mrm.1138
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Nonmonoexponential MR diffusion decay behavior has been observed at high diffusion-weighting strengths for cell aggregates and tissues, including the myocardium; however, implications for myocardial MR diffusion tenser imaging are largely unknown. In this study, a slow-exchange-limit, two-component diffusion tenser model was fitted to diffusion-weighted images obtained in isolated, perfused rat hearts. Results indicate that there are at least two distinct components of anisotropic diffusion, characterized by a "fast" component whose principal diffusivity is comparable to that of the perfusate, and a highly anisotropic "slow" component. It is speculated that the two components correspond to tissue compartments and have a general agreement with the orientations of anisotropy, or fiber orientations, in the myocardium. Moreover, consideration of previous studies of myocardial diffusion suggests that the presently observed fast component may likely be dominated by diffusion in the vascular space, whereas the slow component may include the intracellular and interstitial compartments. The implications of the results for myocardial fiber orientation mapping and limitations of the current two-component model used are also discussed. (C) 2001 Wiley-Liss, Inc.
引用
收藏
页码:1039 / 1045
页数:7
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