» Articles » PMID: 29153927

1Hz RTMS of the Right Orbitofrontal Cortex for Major Depression: Safety, Tolerability and Clinical Outcomes

Overview
Publisher Elsevier
Specialties Pharmacology
Psychiatry
Date 2017 Nov 21
PMID 29153927
Citations 30
Authors
Affiliations
Soon will be listed here.
Abstract

Conventional rTMS in major depressive disorder (MDD) targets the dorsolateral prefrontal cortex (DLPFC). However, many patients do not respond to DLPFC-rTMS. Recent evidence suggests that the right lateral orbitofrontal cortex (OFC) plays a key role in 'non-reward' functions and shows hyperconnectivity in MDD. OFC-rTMS has been used successfully in obsessive-compulsive disorder, and achieved remission in an MDD case nonresponsive to DLPFC- and DMPFC-rTMS. Here, we assess the safety and tolerability of right OFC-rTMS, and examine the effectiveness of inhibitory right OFC-rTMS in MDD, particularly among patients with previous nonresponse to DMPFC-rTMS. We performed a chart review to retrieve data on clinical characteristics, stimulation parameters, adverse events, and clinical symptom outcomes for a series of 42 patients with medication-resistant and/or DMPFC-rTMS-nonresponsive MDD, who underwent 20-30 sessions of 1Hz right OFC-rTMS at a single Canadian clinic from 2015 to 2017. Over 882 sessions of treatment, there were no seizures, visual/ocular complications, or other serious or treatment-limiting adverse events. Pain ratings averaged 6-7/10 (10=maximum tolerable); no patient discontinued treatment prematurely due to pain. 15/42 patients (35.7%) achieved response (≥50% symptom reduction) and 10/42 (23.8%) achieved remission. Among the 30/42 patients who were previous nonresponders to DMPFC-rTMS, 9/30 (30.0%) achieved response and 7/30 (23.8%) achieved remission. Response distribution was sharply bimodal. 1Hz right OFC-rTMS appears safe and tolerable, and may achieve remission in MDD patients even when conventional rTMS has failed. Sham-controlled follow-up studies may be warranted.

Citing Articles

A Narrative Review of the Efficacy of Long COVID Interventions on Brain Fog, Processing Speed, and Other Related Cognitive Outcomes.

Whitaker-Hardin B, McGregor K, Uswatte G, Lokken K Biomedicines. 2025; 13(2).

PMID: 40002834 PMC: 11853337. DOI: 10.3390/biomedicines13020421.


Mechanisms underlying the spontaneous reorganization of depression network after stroke.

Fang Y, Chao X, Lu Z, Huang H, Shi R, Yin D Neuroimage Clin. 2024; 45:103723.

PMID: 39673941 PMC: 11699604. DOI: 10.1016/j.nicl.2024.103723.


A novel dual-site OFC-dlPFC accelerated repetitive transcranial magnetic stimulation for depression: a pilot randomized controlled study.

Cui H, Ding H, Hu L, Zhao Y, Shu Y, Voon V Psychol Med. 2024; :1-14.

PMID: 39440449 PMC: 11578911. DOI: 10.1017/S0033291724002289.


Quantitative MRI at 7-Tesla reveals novel frontocortical myeloarchitecture anomalies in major depressive disorder.

Heij J, van der Zwaag W, Knapen T, Caan M, Forstman B, Veltman D Transl Psychiatry. 2024; 14(1):262.

PMID: 38902245 PMC: 11190139. DOI: 10.1038/s41398-024-02976-y.


Mechanisms of Action of TMS in the Treatment of Depression.

Downar J, Siddiqi S, Mitra A, Williams N, Liston C Curr Top Behav Neurosci. 2024; 66:233-277.

PMID: 38844713 DOI: 10.1007/7854_2024_483.