The Impact of Accelerated High Frequency rTMS on Brain Neurochemicals in Treatment-Resistant Depression: Insights from 1H MR Spectroscopy

TITLE
The Impact of Accelerated High Frequency rTMS on Brain Neurochemicals in Treatment-Resistant Depression: Insights from 1H MR Spectroscopy

AUTHORS
Baeken C; Lefaucheur JP; Van Schuerbeek P.

SOURCE
Clinical Neurophysiology. 128(9):1664-1672, 2017 Sep

OBJECTIVE
Although accelerated repetitive transcranial magnetic stimulation (rTMS) designs seem to be able to alleviate mood over a relatively short period of time, no studies yet examined the cellular effects on neurochemicals with regard to working mechanisms, safety and neural integrity.

METHODS
Eighteen right-handed antidepressant-free unipolar treatment resistant depressed (TRD) patients participated in this sham-controlled accelerated high frequency (aHF)-rTMS 1H MR spectroscopy study applied to the left dorsolateral prefrontal cortex (DLPFC). Baseline measurements were compared to eighteen age- and gender-matched healthy controls. We explicitly focused on neurochemical concentrations in the bilateral DLPFC and rostral anterior cingulate cortex (rACC).

RESULTS
Compared to healthy individuals, TRD patients displayed significantly lower baseline glutamatergic (sum absolute concentrations glutamate and glutamine) concentrations in the left DLPFC. aHF-rTMS does not significantly alter neurochemical concentrations in the three predefined brain regions. Clinical improvement was related to significant GABA concentration increases in the left DLPFC.

CONCLUSIONS
CONCLUSIONS: Accelerated HF-rTMS treatment did not affect neural integrity in the examined regions. The observed GABA concentration increases suggest that the immediate therapeutic effects of aHF-rTMS could be mediated through a locally increased GABAergic inhibitory neurotransmission.

SIGNIFICANCE
Although more statistical power is needed for reaching firm conclusions, aHF-rTMS does not appear to negatively influence neural integrity.

Copyright © 2017 International Federation of Clinical Neurophysiology. Published by Elsevier B.V. All rights reserved.