A multi-compartmental SE-BOLD interpretation for stimulus-related signal changes in diffusion-weighted functional MRI

被引:12
|
作者
Kershaw, Jeff [1 ]
Tomiyasu, Moyoko [1 ]
Kashikura, Kenichi [2 ]
Hirano, Yoshiyuki [1 ]
Nonaka, Hiroi [1 ]
Hirano, Masaya [3 ]
Ikehira, Hiroo [1 ]
Kanno, Iwao [1 ]
Obata, Takayuki [1 ]
机构
[1] Natl Inst Radiol Sci, Mol Imaging Ctr, Dept Biophys, Inage Ku, Chiba 2638555, Japan
[2] Gunma Prefectural Coll Hlth Sci, Sch Radiol Technol, Maebashi, Gunma 3710052, Japan
[3] GE Yokogawa Med Syst Ltd, Imaging Applicat Technol Ctr, Hino, Tokyo 1918503, Japan
关键词
ADC; biexponential signal decay; diffusion-weighting decomposition; functional MRI; spin-echo BOLD; HIGH B-VALUES; WATER DIFFUSION; HUMAN BRAIN; NEURONAL ACTIVATION; COEFFICIENT; CONTRAST; COMPARTMENTATION; BOUNDARIES; PERFUSION; CORTEX;
D O I
10.1002/nbm.1391
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new interpretation is proposed for stimulus-induced signal changes in diffusion-weighted functional MRI. T-2-weighted spin-echo echo-planar images were acquired at different diffusion-weightings while visual stimulation was presented to human volunteers. The amplitudes of the positive stimulus-correlated response and post-stimulus undershoot (PSU) in the functional time-courses were found to follow different trends as a function of b-value. Data were analysed using a three-compartment signal model, with one compartment being purely vascular and the other two dominated by fast- and slow-diffusing molecules in the brain tissue. The diffusion coefficients of the tissue were assumed to be constant throughout the experiments. It is shown that the stimulus-induced signal changes can be decomposed into independent contributions originating from each of the three compartments. After decomposition, the fast-diffusion phase displays a substantial PSU, while the slow-diffusion phase demonstrates a highly reproducible and stimulus-correlated time-course with minimal undershoot. The decomposed responses are interpreted in terms of the spin-echo blood oxygenation level dependent (SE-BOLD) effect, and it is proposed that the signal produced by fast- and slow-diffusing molecules reflect a sensitivity to susceptibility changes in arteriole/venule- and capillary-sized vessels, respectively. This interpretation suggests that diffusion-weighted SE-BOLD imaging may provide subtle information about the haemodynamic and neuronal responses. Copyright (C) 2009 John Wiley & Sons, Ltd.
引用
收藏
页码:770 / 778
页数:9
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