Resting fMRI-guided TMS results in subcortical and brain network modulation indexed by interleaved TMS/fMRI

被引:0
作者
Desmond J. Oathes
Jared P. Zimmerman
Romain Duprat
Seda S. Japp
Morgan Scully
Benjamin M. Rosenberg
Matthew W. Flounders
Hannah Long
Joseph A. Deluisi
Mark Elliott
Gavriella Shandler
Russell T. Shinohara
Kristin A. Linn
机构
[1] University of Pennsylvania Perelman School of Medicine,Department of Psychiatry, Center for Neuromodulation in Depression and Stress
[2] University of Pennsylvania Perelman School of Medicine,Department of Neuroscience
[3] University of California Los Angeles,Department of Psychology
[4] University of Pennsylvania Perelman School of Medicine,Department of Radiology, Center for Magnetic Resonance and Optical Imaging
[5] University of Pennsylvania Perelman School of Medicine,Department of Biostatistics, Epidemiology, and Informatics, Penn Statistics in Imaging and Visualization Center
[6] University of Pennsylvania Perelman School of Medicine,Center for Biomedical Image Computing and Analytics
来源
Experimental Brain Research | 2021年 / 239卷
关键词
TMS; fMRI; Neuroimaging; Anxiety; Depression;
D O I
暂无
中图分类号
学科分类号
摘要
Traditional non-invasive imaging methods describe statistical associations of functional co-activation over time. They cannot easily establish hierarchies in communication as done in non-human animals using invasive methods. Here, we interleaved functional MRI (fMRI) recordings with non-invasive transcranial magnetic stimulation (TMS) to map causal communication between the frontal cortex and subcortical target structures including the subgenual anterior cingulate cortex (sgACC) and the amygdala. Seed-based correlation maps from each participant’s resting fMRI scan determined individual stimulation sites with high temporal correlation to targets for the subsequent TMS/fMRI session(s). The resulting TMS/fMRI images were transformed to quantile responses, so that regions of high-/low-quantile response corresponded to the areas of the brain with the most positive/negative evoked response relative to the global brain response. We then modeled the average quantile response for a given region (e.g., structure or network) to determine whether TMS was effective in the relative engagement of the downstream targets. Both the sgACC and amygdala were differentially influenced by TMS. Furthermore, we found that the sgACC distributed brain network was modulated in response to fMRI-guided TMS. The amygdala, but not its distributed network, also responded to TMS. Our findings suggest that individual targeting and brain response measurements reflect causal circuit mapping to the sgACC and amygdala in humans. These results set the stage to further map circuits in the brain and link circuit pathway integrity to clinical intervention outcomes, especially when the intervention targets specific pathways and networks as is possible with TMS.
引用
收藏
页码:1165 / 1178
页数:13
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