The effect of slice order and thickness on fMRI activation data using multislice echo-planar imaging

被引:35
作者
Howseman, AM
Grootoonk, S
Porter, DA
Ramdeen, J
Holmes, AP
Turner, R
机构
[1] Inst Neurol, Wellcome Dept Cognit Neurol, London WC1N 3BG, England
[2] UCL, Inst Child Hlth, London, England
[3] Great Ormond St Hosp Sick Children, NMR Unit, London WC1N 3BG, England
[4] Univ Surrey, Dept Phys, Guildford, Surrey, England
基金
英国惠康基金;
关键词
multislice EPI; slice order and thickness; fMRI;
D O I
10.1006/nimg.1998.0418
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Multislice echo-planar imaging (EPI) is a commonly used technique for fMRI studies. Brain activation images acquired using fMRI are sensitive to T(2)* changes, reflecting the level of blood oxygenation (BOLD contrast), and may also contain an element of T(1) contrast which detects blood how changes in large vessels. If slice inflow (T(1)) effects are significant in multislice EPI, then as the order in which the slices are acquired is changed, differences in the activation maps are predicted. However, in experiments presented here using visual stimulation, the data demonstrate that highly consistent results can be achieved for repetition times (TR) of 6.0, 3.0, and 1.5 s. This suggests that, for whole-brain multislice EPI, fMRI activation is dominated by T(2)*, BOLD contrast. The thickness of the imaging slice is also an important parameter in these studies, having implications for spatial resolution, sensitivity, and acquisition time. In separate visual cortex experiments the effect on the values of the fMRI Z scores and the number of activated voxels is investigated as a function of slice thickness (from 1 to 8 mm). The maximum Z scores in the data are similar for all slice thicknesses and, after resampling to allow a direct comparison to be made, the volume of visual cortex detected as significantly activated increases with slice thickness. (C) 1999 Academic Press.
引用
收藏
页码:363 / 376
页数:14
相关论文
共 29 条
  • [1] SPIN-ECHO AND GRADIENT-ECHO EPI OF HUMAN BRAIN ACTIVATION USING BOLD CONTRAST - A COMPARATIVE-STUDY AT 1.5 T
    BANDETTINI, PA
    WONG, EC
    JESMANOWICZ, A
    HINKS, RS
    HYDE, JS
    [J]. NMR IN BIOMEDICINE, 1994, 7 (1-2) : 12 - 20
  • [2] THE INTRAVASCULAR CONTRIBUTION TO FMRI SIGNAL CHANGE - MONTE-CARLO MODELING AND DIFFUSION-WEIGHTED STUDIES IN-VIVO
    BOXERMAN, JL
    BANDETTINI, PA
    KWONG, KK
    BAKER, JR
    DAVIS, TL
    ROSEN, BR
    WEISSKOFF, RM
    [J]. MAGNETIC RESONANCE IN MEDICINE, 1995, 34 (01) : 4 - 10
  • [3] Functional magnetic resonance neuroimaging data acquisition techniques
    Duyn, JH
    Yang, YH
    Frank, JA
    Mattay, VS
    Hou, L
    [J]. NEUROIMAGE, 1996, 4 (03) : S76 - S83
  • [4] INFLOW VERSUS DEOXYHEMOGLOBIN EFFECTS IN BOLD FUNCTIONAL MRI USING GRADIENT ECHOES AT 1.5 T
    DUYN, JH
    MOONEN, CTW
    VANYPEREN, GH
    DEBOER, RW
    LUYTEN, PR
    [J]. NMR IN BIOMEDICINE, 1994, 7 (1-2) : 83 - 88
  • [5] FOCAL PHYSIOLOGICAL UNCOUPLING OF CEREBRAL BLOOD-FLOW AND OXIDATIVE-METABOLISM DURING SOMATOSENSORY STIMULATION IN HUMAN-SUBJECTS
    FOX, PT
    RAICHLE, ME
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (04) : 1140 - 1144
  • [6] FUNCTIONAL MRI OF HUMAN BRAIN ACTIVATION AT HIGH SPATIAL-RESOLUTION
    FRAHM, J
    MERBOLDT, KD
    HANICKE, W
    [J]. MAGNETIC RESONANCE IN MEDICINE, 1993, 29 (01) : 139 - 144
  • [7] BRAIN OR VEIN-OXYGENATION OR FLOW - ON SIGNAL PHYSIOLOGY IN FUNCTIONAL MRI OF HUMAN BRAIN ACTIVATION
    FRAHM, J
    MERBOLDT, KD
    HANICKE, W
    KLEINSCHMIDT, A
    BOECKER, H
    [J]. NMR IN BIOMEDICINE, 1994, 7 (1-2) : 45 - 53
  • [8] Friston K., 1995, HUM BRAIN MAP, V2, P165, DOI DOI 10.1002/HBM.460030303
  • [9] Friston K., 1994, HUM BRAIN MAPP, V1, P153, DOI DOI 10.1002/HBM.460010207
  • [10] Friston K J, 1994, Hum Brain Mapp, V1, P210, DOI 10.1002/hbm.460010306