Arterial spin-labeled perfusion MRI in basic and clinical neuroscience

被引:175
作者
Detre, John A. [1 ,2 ,4 ]
Wang, Jiongjiong [2 ,4 ]
Wang, Ze [3 ,4 ]
Rao, Hengyi [3 ,4 ]
机构
[1] Univ Penn, Dept Neurol, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Psychiat, Philadelphia, PA 19104 USA
[4] Univ Penn, Ctr Funct Neuroimaging, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
brain function; cerebral blood flow; magnetic resonance imaging; neuroimaging; CEREBRAL-BLOOD-FLOW; ALZHEIMER-DISEASE; NEURAL ACTIVITY; BRAIN ACTIVITY; CBF CHANGES; FMRI; HYPOPERFUSION; INVERSION; QUANTIFICATION; SENSITIVITY;
D O I
10.1097/WCO.0b013e32832d9505
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Purpose of review Arterial spin labeling (ASL) provides an endogenous and completely noninvasive tracer for the quantification of regional cerebral blood flow (CBF) with magnetic resonance imaging (MRI). Although the measurement of CBF has obvious utility in cerebrovascular disorders, because CBF is closely coupled to neural metabolism, ASL perfusion MRI has a broad range of potential applications as a biomarker of regional brain function in basic and clinical neuroscience. Recent findings Over the past few years, ASL technology has improved considerably and the utility of ASL perfusion MRI as a diagnostic and research tool has been demonstrated. This review briefly covers ASL methodologies and clinical applications, while expanding on the use of ASL in human neuroscience research to elucidate patterns of resting brain function that correlate with genotype or phenotype (trait effects), or in response to exogenous manipulations of brain function with pharmacological agents or psychological tasks (slate effects). Summary ASL perfusion MRI provides a versatile biomarker of regional brain function that can be acquired as part of a multimodal MRI examination. Because ASL quantifies a physiological parameter, it should be useful for multisite or longitudinal studies.
引用
收藏
页码:348 / 355
页数:8
相关论文
共 73 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]
Hippocampal hyperperfusion in Alzheimer's disease [J].
Alsop, David C. ;
Casement, Melynda ;
de Bazelaire, Cedric ;
Fong, Tamara ;
Press, Daniel Z. .
NEUROIMAGE, 2008, 42 (04) :1267-1274
[3]
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
[4]
Alsop DC, 2000, ANN NEUROL, V47, P93, DOI 10.1002/1531-8249(200001)47:1<93::AID-ANA15>3.0.CO
[5]
2-8
[6]
Caudate blood flow and volume are reduced in HIV+ neurocognitively impaired patients [J].
Ances, BM ;
Roc, AC ;
Wang, J ;
Korczykowski, M ;
Okawa, J ;
Stern, J ;
Kim, J ;
Wolf, R ;
Lawler, K ;
Kolson, DL ;
Detre, JA .
NEUROLOGY, 2006, 66 (06) :862-866
[7]
Voxel-based morphometry - The methods [J].
Ashburner, J ;
Friston, KJ .
NEUROIMAGE, 2000, 11 (06) :805-821
[8]
Age dependence of cerebral perfusion assessed by magnetic resonance continuous arterial spin labeling [J].
Biagi, Laura ;
Abbruzzese, Arturo ;
Bianchi, Maria Cristina ;
Alsop, David C. ;
Del Guerra, Alberto ;
Tosetti, Michela .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2007, 25 (04) :696-702
[9]
Quantifying CBF with arterial spin labeling [J].
Buxton, RB .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2005, 22 (06) :723-726
[10]
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