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Exploring the predictive power of iTBS induced prefrontal excitability using concurrent TBS/fNIRS
Rebecca L D Kan1, Linsen Li2, Teng Liu1
1Department of Rehabilitation Sciences, The Hong Kong Polytechnic University, Kowloon, Hong Kong SAR, China.
A single session of intermittent theta-burst stimulation (iTBS) to the dorsolateral prefrontal cortex (DLPFC) changes cortical excitability but does not improve working memory in healthy individuals. iTBS-induced excitability changes did not predict working memory performance.
Area of Science:
- Neuroscience
- Cognitive Science
- Neuromodulation
Background:
- The impact of single-session intermittent theta-burst stimulation (iTBS) on dorsolateral prefrontal cortex (DLPFC) function is not fully understood.
- The clinical utility of predicting DLPFC function based on iTBS-induced excitability remains unexplored.
Purpose of the Study:
- To investigate the immediate effects of a single iTBS session on DLPFC function and cortical excitability.
- To determine if iTBS-induced prefrontal cortical excitability can predict working memory performance.
Main Methods:
- A randomized, sham-controlled, crossover study involving 30 healthy participants.
- Concurrent iTBS and functional near-infrared spectroscopy (fNIRS) were used to measure prefrontal hemoglobin concentrations.
- Working memory was assessed using the 3-back task before and after stimulation.
Main Results:
- No significant difference in 3-back task performance between active and sham iTBS.
- A significant decrease in iTBS-induced oxygen-hemoglobin (HbO) change in the active group compared to sham.
- iTBS-induced HbO changes did not significantly predict working memory performance at any timepoint.
Conclusions:
- A single iTBS session to the left DLPFC induces immediate cortical excitability changes but does not enhance working memory compared to sham.
- iTBS-induced prefrontal excitability does not predict subsequent working memory performance after a single session.
- Further research with larger sample sizes is needed to explore iTBS-induced excitability as a potential imaging marker for clinical treatment response.
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