Comparison of quantitative perfusion imaging using arterial spin labeling at 1.5 and 4.0 tesla

被引:288
作者
Wang, JJ
Alsop, DC
Li, L
Listerud, J
Gonzalez-At, JB
Schnall, MD
Detre, JA
机构
[1] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Radiol, Ctr Comp, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
[4] Univ Penn, Dept Metab Magnet Resonance Res, Philadelphia, PA 19104 USA
[5] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Dept Radiol, Boston, MA USA
关键词
arterial spin labeling (ASL); cerebral blood flow (CBF); magnetic field strength; multislice perfusion fMRI; susceptibility effect;
D O I
10.1002/mrm.10211
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
High-field arterial spin labeling (ASL) perfusion MRI is appealing because it provides not only increased signal-to-noise ratio (SNR), but also advantages in terms of labeling due to the increased relaxation time T, of labeled blood. In the present study, we provide a theoretical framework for the dependence of the ASL signal on the static field strength, followed by experimental validation in which a multislice pulsed ASL (PASL) technique was carried out at 4T and compared with PASL and continuous ASL (CASL) techniques at 1.5T, both in the resting state and during motor activation. The resting-state data showed an SNR ratio of 2.3:1.4:1 in the gray matter and a contrast-to-noise ratio (CNR) of 2.7:1.1:1 between the gray and white matter for the difference perfusion images acquired using 4T PASL, 1.5T CASL, and 1.5T PASL, respectively. However, the functional data acquired using 4T PASL did not show significantly improved sensitivity to motor cortex activation compared with the 1.5T functional data, with reduced fractional perfusion signal change and increased intersubject variability. Possible reasons for these experimental results, including susceptibility effects and physiological noise, are discussed.
引用
收藏
页码:242 / 254
页数:13
相关论文
共 47 条
[1]   Experimental design and the relative sensitivity of BOLD and perfusion fMRI [J].
Aguirre, GK ;
Detre, JA ;
Zarahn, E ;
Alsop, DC .
NEUROIMAGE, 2002, 15 (03) :488-500
[2]  
ALSOP DA, 2001, P 9 ANN M ISMRM GLAS, P1562
[3]   Multisection cerebral blood flow MR imaging with continuous arterial spin labeling [J].
Alsop, DC ;
Detre, JA .
RADIOLOGY, 1998, 208 (02) :410-416
[4]   Reduced transit-time sensitivity in noninvasive magnetic resonance imaging of human cerebral blood flow [J].
Alsop, DC ;
Detre, JA .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1996, 16 (06) :1236-1249
[5]  
Alsop DC, 2000, ANN NEUROL, V47, P93, DOI 10.1002/1531-8249(200001)47:1<93::AID-ANA15>3.0.CO
[6]  
2-8
[7]   A REVIEW OF H-1 NUCLEAR-MAGNETIC-RESONANCE RELAXATION IN PATHOLOGY - ARE T1 AND T2 DIAGNOSTIC [J].
BOTTOMLEY, PA ;
HARDY, CJ ;
ARGERSINGER, RE ;
ALLENMOORE, G .
MEDICAL PHYSICS, 1987, 14 (01) :1-37
[8]   A general kinetic model for quantitative perfusion imaging with arterial spin labeling [J].
Buxton, RB ;
Frank, LR ;
Wong, EC ;
Siewert, B ;
Warach, S ;
Edelman, RR .
MAGNETIC RESONANCE IN MEDICINE, 1998, 40 (03) :383-396
[9]   Magnetic resonance perfusion imaging in acute ischemic stroke using continuous arterial spin labeling [J].
Chalela, JA ;
Alsop, DC ;
Gonzalez-Atavales, JB ;
Maldjian, JA ;
Kasner, SE ;
Detre, JA .
STROKE, 2000, 31 (03) :680-687
[10]   STAR-HASTE: Perfusion imaging without magnetic susceptibility artifact [J].
Chen, Q ;
Siewert, B ;
Bly, BM ;
Warach, S ;
Edelman, RR .
MAGNETIC RESONANCE IN MEDICINE, 1997, 38 (03) :404-408