Why the study?
rTMS lacks reliable biomarkers of treatment response, prompting investigation into whether low frequency 1 Hz R-DLPFC rTMS affects cardiac activity in MDD and if ECG parameters can serve as outcome biomarkers.
Does accelerated 1 Hz R-DLPFC rTMS induce changes in heart rate that predict treatment outcome in patients with major depressive disorder?
Does accelerated 1 Hz R-DLPFC rTMS induce changes in heart rate that predict treatment outcome in patients with major depressive disorder?
Resting heart rate and rTMS-induced heart rate reduction may serve as potential biomarkers for treatment response to low-frequency rTMS in major depressive disorder.
Cardiac activity changes may indicate low-frequency DLPFC rTMS response in MDD; leaves open validation as a reliable biomarker.
BACKGROUND AND OBJECTIVE: Repetitive transcranial magnetic stimulation (rTMS) is an effective and safe treatment for major depressive disorder (MDD). rTMS is in need of a reliable biomarker of treatment response. High frequency (HF) dorsolateral prefrontal cortex (DLPFC) rTMS has been reported to induce significant changes in the cardiac activity of MDD patients. Low frequency DLPFC rTMS has many advantages over HF-DLPFC rTMS and thus this study aims to further investigate the effect of low frequency 1 Hz right hemisphere (R)-DLPFC rTMS on the cardiac activity of MDD patients, as well as the potential of using electrocardiogram (ECG) parameters as biomarkers of treatment outcome. METHODS: Baseline ECG sessions were performed for 19 MDD patients. All patients then underwent 40 sessions of accelerated 1 Hz R-DLPFC rTMS one week after the baseline session. RESULTS: Heart rate (HR) significantly decreased from the resting period to the first and third minute of the 1 Hz R-DLPFC rTMS period. Resting HR was found to have a significant negative association with treatment outcome. Prior to Bonferroni correction, HR during stimulation and the degree of rTMS-induced HR reduction were significantly negatively associated with treatment outcome. No significant changes were observed for the heart rate variability (HRV) parameters. LIMITATIONS: Sample size (n = 19); the use of electroencephalography equipment for ECG; lack of respiration monitoring; relatively short recording duration for HRV parameters. CONCLUSION: This novel study provides further preliminary evidence that ECG may be utilized as a biomarker of rTMS treatment response in MDD. TRIAL REGISTRATION: ClinicalTrials.gov Identifier: NCT04376697.
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Sheen et al. (2022) studied this question.
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