TY - JOUR
T1 - Optimization of phase-contrast MRI for the estimation of global cerebral blood flow of mice at 11.7T
AU - Wei, Zhiliang
AU - Chen, Lin
AU - Lin, Zixuan
AU - Jiang, Dengrong
AU - Xu, Jiadi
AU - Liu, Peiying
AU - van Zijl, Peter C.M.
AU - Lu, Hanzhang
N1 - Funding Information:
Funding Information NIH R01 MH084021, NIH R01 NS106702, NIH R01 NS106711, NIH R01 AG047972, NIH R21 AG058413, NIH R21 NS095342, NIH R21 NS085634, and NIH P41 EB015909
Publisher Copyright:
© 2018 International Society for Magnetic Resonance in Medicine
PY - 2019/4
Y1 - 2019/4
N2 - Purpose: To optimize phase-contrast (PC) MRI for the measurement of global cerebral blood flow (CBF) in the mouse at 11.7T. Methods: We determined proper velocity encoding (VENC) for internal carotid arteries (ICAs) and vertebral arteries (VAs). Next, we optimized spatial resolution of the sequence. To shorten scan time without compromising data quality, we further optimized repetition time and developed a reduced field-of-view (FOV) scheme for ICA and VA PC MRI. Whole-brain volume was determined with T2-weighted image to obtain unit-volume CBF. Results: Peak flow velocities were 13.8 ± 1.7, 14.4 ± 0.6, 6.5 ± 1.7, and 6.7 ± 1.3 cm/s for left ICA, right ICA, left VA, and right VA, respectively. Thus, VENC values of 20 and 10 cm/s were chosen for ICA and VA PC MRI, respectively. An in-plane spatial resolution of 50 × 50 μm2 was found to provide a reasonable trade-off between reducing partial-volume effects and maintaining signal-to-noise ratio. Because of the fact that saturated spins in the imaging slice are rapidly replaced by fresh spins, TR of the sequence can be decreased to as short as 15 ms without reducing signal intensity, thereby substantially lowering scan time. Moreover, reduced FOV along the phase-encoding direction was able to shorten scan time by 33.3% while maintaining measurement accuracy. With these optimizations, it took 96 seconds to evaluate CBF with a test-retest variability of approximately 5% and an inter-rater correlation of >0.95. Global unit-volume CBF was found to be 279.5 ± 11.1 mL of blood/100 ml of tissue/min. Conclusion: We have optimized PC MRI for noninvasive quantification of blood flow in mice at 11.7T.
AB - Purpose: To optimize phase-contrast (PC) MRI for the measurement of global cerebral blood flow (CBF) in the mouse at 11.7T. Methods: We determined proper velocity encoding (VENC) for internal carotid arteries (ICAs) and vertebral arteries (VAs). Next, we optimized spatial resolution of the sequence. To shorten scan time without compromising data quality, we further optimized repetition time and developed a reduced field-of-view (FOV) scheme for ICA and VA PC MRI. Whole-brain volume was determined with T2-weighted image to obtain unit-volume CBF. Results: Peak flow velocities were 13.8 ± 1.7, 14.4 ± 0.6, 6.5 ± 1.7, and 6.7 ± 1.3 cm/s for left ICA, right ICA, left VA, and right VA, respectively. Thus, VENC values of 20 and 10 cm/s were chosen for ICA and VA PC MRI, respectively. An in-plane spatial resolution of 50 × 50 μm2 was found to provide a reasonable trade-off between reducing partial-volume effects and maintaining signal-to-noise ratio. Because of the fact that saturated spins in the imaging slice are rapidly replaced by fresh spins, TR of the sequence can be decreased to as short as 15 ms without reducing signal intensity, thereby substantially lowering scan time. Moreover, reduced FOV along the phase-encoding direction was able to shorten scan time by 33.3% while maintaining measurement accuracy. With these optimizations, it took 96 seconds to evaluate CBF with a test-retest variability of approximately 5% and an inter-rater correlation of >0.95. Global unit-volume CBF was found to be 279.5 ± 11.1 mL of blood/100 ml of tissue/min. Conclusion: We have optimized PC MRI for noninvasive quantification of blood flow in mice at 11.7T.
KW - cerebral blood flow
KW - internal carotid artery
KW - maximum blood velocity
KW - partial volume effect
KW - spatial folding
KW - spatial resolution
KW - vertebral artery
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U2 - 10.1002/mrm.27592
DO - 10.1002/mrm.27592
M3 - Article
C2 - 30393888
AN - SCOPUS:85056144645
SN - 0740-3194
VL - 81
SP - 2566
EP - 2575
JO - Magnetic resonance in medicine
JF - Magnetic resonance in medicine
IS - 4
ER -