Work

Theta burst stimulation prior to stress exposure alters amplitude of low-frequency fluctuations

Year: 2026
Type: article
Study design: Clinical Trial
Abstract: BACKGROUND: The Amplitude of Low-Frequency Fluctuations (ALFF) serves as a marker of spontaneous neural activity, with previous research showing increased ALFF during rumination induction. However, it remains unclear whether Theta Burst Stimulation (TBS) might be able to modulate ALFF. METHODS: In two studies, we applied intermittent (iTBS) and continuous (cTBS) TBS protocols to the left Dorsolateral Prefrontal Cortex (DLPFC; study 1) and right Ventrolateral Prefrontal Cortex (VLPFC; study 2) prior to the Trier Social Stress Test (TSST). Neural activity was assessed using functional near-infrared spectroscopy (fNIRS), an optical imaging technique measuring cortical oxygenation, from which ALFF was derived. In both studies (study 1: n = 88; study 2: n = 89) low and high trait ruminators were recruited. Each participant underwent both active (iTBS or cTBS) and sham TBS (sTBS) in a randomized, counterbalanced, double-blind design. We fitted rmANOVAs examining the effects of time, trait rumination, TBS condition and regions of interest (ROIs) for each stimulation target. RESULTS: Results indicated stress-related increases in ALFF across all ROIs, including the DLPFC, VLPFC, and Somatosensory Association Cortex. We found partial evidence for TBS-induced modulation of frontal ALFF; however, blinding was partly unsuccessful: In study 2, targeting the right VLPFC, both cTBS and sTBS were associated with increases in ALFF from the pre-TSST resting state to the TSST, followed by decreases from the TSST to the post-TSST resting state. This effect was absent following iTBS and when reanalyzing effects using Percent ALFF. CONCLUSION: Our findings suggest that TBS might modulate ALFF, highlighting the need for further investigation of factors such as rumination.
Language: English
Subfield: Neurology
Open Access status: hybrid
Estimated APC paid: $3,440
OpenAlex ID: W7160424741
FWCI:
Cites: 74
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