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Volume 55, Issue 9, Pages 882-890 (1 May 2004)


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Acute left prefrontal transcranial magnetic stimulation in depressed patients is associated with immediately increased activity in prefrontal cortical as well as subcortical regions

Xingbao LiabCorresponding Author Information, Ziad Nahasab, F.Andrew Kozelabd, Berry Andersona, Daryl E Bohningc, Mark S Georgeabcd

Received 9 October 2003; received in revised form 7 January 2004; accepted 13 January 2004.

Abstract 

Background

Focal prefrontal cortex repetitive transcranial magnetic stimulation (rTMS) was originally investigated as a potential antidepressant under the assumption that in depressed patients, prefrontal cortex stimulation would produce changes in connected limbic regions involved in mood regulation.

Methods

Fourteen adult patients with depression were scanned in a 1.5-T scanner using interleaved rTMS (1 Hz) applied on the left prefrontal cortex over 7.35 min. Images were analyzed with Statistical Parametric Mapping 2b and principal component analysis.

Results

Over the left prefrontal cortex, 1-Hz TMS was associated with increased activity at the site of stimulation as well as in connected limbic regions: bilateral middle prefrontal cortex, right orbital frontal cortex, left hippocampus, mediodorsal nucleus of the thalamus, bilateral putamen, pulvinar, and insula (t = 3.85, p < .001). Significant deactivation was found in the right ventromedial frontal cortex.

Conclusions

In depressed patients, 1-Hz TMS at 100% motor threshold over the left prefrontal cortex induces activation underneath the coil, activates frontal–subcortical neuronal circuits, and decreases activity in the right ventromedial cortex. Further work is needed to understand whether these immediate changes vary as a function of TMS use parameters (intensity, frequency, location) and whether they relate to neurobiologic effects and antidepressant mechanisms of TMS.

a Brain Stimulation Laboratory, Department of Psychiatry, Charleston, South Carolina, USA

b Center for Advanced Imaging Research, Charleston, South Carolina, USA

c Department of Radiology, Medical University of South Carolina, Charleston, South Carolina, USA

d Mental Health Service, Ralph H. Johnson Department of Veterans Affairs Medical Center, Charleston, South Carolina, USA

Corresponding Author InformationAddress reprint requests to Dr. Xingbao Li, Brain Stimulation Laboratory, MUSC IOP, Room 502 North, 67 President Street, Charleston, SC 29425, USA

PII: S0006-3223(04)00103-9

doi:10.1016/j.biopsych.2004.01.017


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