Personalized repetitive transcranial magnetic stimulation temporarily alters default mode network in healthy subjects. View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2019-12

AUTHORS

Aditya Singh, Tracy Erwin-Grabner, Grant Sutcliffe, Andrea Antal, Walter Paulus, Roberto Goya-Maldonado

ABSTRACT

High frequency repetitive transcranial magnetic stimulation (HF-rTMS) delivered to the left dorsolateral prefrontal cortex (DLPFC) is an effective treatment option for treatment resistant depression. However, the underlying mechanisms of a full session of HF-rTMS in healthy volunteers have not yet been described. Here we investigated, with a personalized selection of DLPFC stimulation sites, the effects driven by HF-rTMS in healthy volunteers (n = 23) over the default mode network (DMN) in multiple time windows. After a complete 10 Hz rTMS (3000 pulses) session, we observe a decrease of functional connectivity between the DMN and the subgenual Anterior Cingulate Cortex (sgACC), as well as the ventral striatum (vStr). A negative correlation between the magnitude of this decrease in the right sgACC and the harm avoidance domain measure from the Temperament and Character Inventory was observed. Moreover, we identify that coupling strength of right vStr with the DMN post-stimulation was proportional to a decrease in self-reports of negative mood from the Positive and Negative Affect Schedule. This shows HF-rTMS attenuates perception of negative mood in healthy recipients in agreement with the expected effects in patients. Our study, by using a personalized selection of DLPFC stimulation sites, contributes understanding the effects of a full session of rTMS approved for clinical use in depression over related brain regions in healthy volunteers. More... »

PAGES

5631

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/s41598-019-42067-3

DOI

http://dx.doi.org/10.1038/s41598-019-42067-3

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1113185011

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30948765


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