Optimizing the experimental design for ankle dorsiflexion fMRI

被引:60
作者
MacIntosh, BJ
Mraz, R
Baker, N
Tam, F
Staines, WR
Graham, SJ
机构
[1] Univ Toronto, Sunnybrook & Womens CHSC, Dept Med Neurol, Toronto, ON M4N 3M5, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M4N 3M5, Canada
[3] York Univ, Dept Kinesiol & Hlth Sci, Toronto, ON M3J 2R7, Canada
基金
加拿大创新基金会; 加拿大健康研究院;
关键词
fMRI; ankle dorsiflexion; event-related design; block design; visual biofeedback; electromyography; simulation;
D O I
10.1016/j.neuroimage.2004.03.035
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Compared to motor studies of the upper limb, few experiments have sought a relationship between blood oxygen level-dependent (BOLD) functional magnetic resonance imaging (fMRI) sensorimotor signals and the resulting lower limb output. In Experiment 1, using an fMRI simulator system, we determined the optimized experimental protocol based on two design types and four behavioral movement types during ankle dorsiflexion. Experiment 2 involved testing the BOLD sensitivity at 1.5 T during ankle movements. Subjects performed large- and small-amplitude dorsiflexion movement types using an event-related design, with the intent of contrasting spatial and temporal features of the BOLD signal. In both experiments, the subject's behavior was guided by visual biofeedback of their ankle flexion angle, using an MR-compatible fiberoptic tape. From Experiment 1, we found electromyography (EMG) difference voltage ratio of approximately 2:1 for large (40degrees) and small (15degrees) dorsiflexion, 0.13 mV and 0.07 mV, respectively. In Experimental 2, we found the peak BOLD % signal changes of 1.04% and 0.89%, for large (40degrees) and small (15degrees) dorsiflexion, respectively. In addition, graded dorsiflexion produced graded BOLD signals in the primary sensorimotor and supplementary motor areas in 10 of 12 healthy young subjects, attesting to the feasibility of lower-limb fMRI at 1.5 T. This study provides insight into the cortical network involved in dorsiflexion using an experimental paradigm that is likely to translate effectively to hemiparetic stroke subjects. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:1619 / 1627
页数:9
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