TY - JOUR
T1 - Transfer insensitive labeling technique (TILT)
T2 - Application to multislice functional perfusion imaging
AU - Golay, Xavier
AU - Stuber, Matthias
AU - Pruessmann, Klaas P.
AU - Meier, Dieter
AU - Boesiger, Peter
PY - 1999/3
Y1 - 1999/3
N2 - Cerebral blood flow can be studied in a multislice mode with a recently proposed perfusion sequence using inversion of water spins as an endogenous tracer without magnetization transfer artifacts. The magnetization transfer insensitive labeling technique (TILT) has been used for mapping blood flow changes at a microvascular level under motor activation in a multislice mode. In TILT, perfusion mapping is achieved by subtraction of a perfusion- sensitized image from a control image. Perfusion weighting is accomplished by proximal blood labeling using two 90°radiofrequency excitation pulses. For control preparation the labeling pulses are modified such that they have no net effect on blood water magnetization. The percentage of blood flow change, as well as its spatial extent, has been studied in single and multislice modes with varying delays between labeling and imaging. The average perfusion signal change due to activation was 36.9 ± 9.1% in the single-slice experiments and 38.1 ± 7.9% in the multislice experiments. The volume of activated brain areas amounted to 1.51 ± 0.95 cm3 in the contralateral primary motor (M1) area, 0.90 ± 0.72 cc in the ipsilateral M1 area, 1.27 ± 0.39 cm3 in the contralateral and 1.42 ± 0.75 cm3 in the ipsilateral premotor areas, and 0.71 ± 0.19 cm3 in the supplementary motor area.
AB - Cerebral blood flow can be studied in a multislice mode with a recently proposed perfusion sequence using inversion of water spins as an endogenous tracer without magnetization transfer artifacts. The magnetization transfer insensitive labeling technique (TILT) has been used for mapping blood flow changes at a microvascular level under motor activation in a multislice mode. In TILT, perfusion mapping is achieved by subtraction of a perfusion- sensitized image from a control image. Perfusion weighting is accomplished by proximal blood labeling using two 90°radiofrequency excitation pulses. For control preparation the labeling pulses are modified such that they have no net effect on blood water magnetization. The percentage of blood flow change, as well as its spatial extent, has been studied in single and multislice modes with varying delays between labeling and imaging. The average perfusion signal change due to activation was 36.9 ± 9.1% in the single-slice experiments and 38.1 ± 7.9% in the multislice experiments. The volume of activated brain areas amounted to 1.51 ± 0.95 cm3 in the contralateral primary motor (M1) area, 0.90 ± 0.72 cc in the ipsilateral M1 area, 1.27 ± 0.39 cm3 in the contralateral and 1.42 ± 0.75 cm3 in the ipsilateral premotor areas, and 0.71 ± 0.19 cm3 in the supplementary motor area.
KW - Brain mapping
KW - Labeling technique
KW - Perfusion imaging
KW - fMRI
UR - http://www.scopus.com/inward/record.url?scp=0032904710&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0032904710&partnerID=8YFLogxK
U2 - 10.1002/(SICI)1522-2586(199903)9:3<454::AID-JMRI14>3.0.CO;2-B
DO - 10.1002/(SICI)1522-2586(199903)9:3<454::AID-JMRI14>3.0.CO;2-B
M3 - Article
C2 - 10194717
AN - SCOPUS:0032904710
SN - 1053-1807
VL - 9
SP - 454
EP - 461
JO - Journal of Magnetic Resonance Imaging
JF - Journal of Magnetic Resonance Imaging
IS - 3
ER -