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Right frontal lobe slow frequency repetitive transcranial magnetic stimulation (SF r-TMS) is an effective treatment for depression: a case-control pilot study of safety and efficacy
  1. Daniel L Menkesa,
  2. Peter Bodnarc,
  3. Roderick A Ballesterosb,
  4. Michael R Swensona
  1. aDepartment of Neurology, University of Louisville, 500 South Presyon Street, HSC 113, Louisville, KY 40202, USA, b60th MDOS/SGOMU, 101 Bodin Circle, Travis AFB, CA 94535, USA, c249 Ballindine Drive, Vacaville, CA 95688, USA
  1. Dr D L Menkes, Department of Neurology, University of Louisville, 500 South Presyon Street, HSC 113, Louisville, KY 40202, USA


Major depression may result from decreased left frontal lobe function with respect to the right. Fast frequency repetitive transcranial magnetic stimulation (FF r-TMS) excites the underlying cortex whereas slow frequency repetitive transcranial magnetic stimulation (SF r-TMS) causes cortical inhibition. Left frontal FF r-TMS attenuates major depression whereas the inhibitory effects of right frontal SF r-TMS are unknown. This study tested the hypothesis that right frontal SF r-TMS would treat depressed patients with minimal effect on controls.

 A psychiatrist administered the Beck depression inventory and Hamilton D depression rating scales to eight depressed patients and six controls before and after the treatment protocol. Eight sessions of 100 right frontal lobe SF r-TMS were given at motor threshold and 0.5 Hz over a 6 week period.  No adverse outcomes were noted in either group. A significant antidepressant effect was noted in depressed patients on the Beck and Hamilton D depression rating scales (p<0.05). No change on either scale was noted in the controls.  In conclusion right frontal lobe SF r-TMS is a safe, non-invasive treatment for major depression that deserves further investigation.

  • transcranial magnetic stimulation
  • depression
  • slow frequency
  • right frontal lobe

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Unipolar depression has an lifetime incidence estimated as between 1.5% and 19%.1 Despite effective medications, treatment failures occur because of the delayed onset of efficacy or intolerable side effects. Biweekly electroconvulsive therapy has a shorter onset latency but it requires anaesthetic agents and seizure induction.2 Moreover, electroconvulsive therapy causes memory impairment in direct proportion to treatment frequency. Transcranial magnetic stimulation given as a single pulse (TMS) or as a train of repetitive stimuli (r-TMS) induces an electric field in the underlying cortex. r-TMS is further subdivided into fast frequency (FF r-TMS) for rates> 1 Hz and slow frequency (SF r-TMS) for rates<1 Hz. Both frequencies induce immediate cortical suppression but only FF r-TMS produces subsequent cortical excitation.3

Mood disorders may result from a relative imbalance of frontal lobe function wherein depression occurs with a hypofunctioning left frontal lobe whereas mania may result from the opposite situation.4 Additional evidence supporting this paradigm is the finding of reduced left frontal lobe glucose metabolism in depressed patients.5 Furthermore, net cortical excitation with left frontal FF r-TMS was effective in treating depression whereas right frontal lobe FF r-TMS treated mania.6 7 However, FF r-TMS has side effects ranging from patient discomfort to seizure induction.8

By contrast, SF r-TMS is neither painful nor epileptogenic. An open, uncontrolled trial conducted subsequent to this one showed therapeutic efficacy of SF r-TMS in depressed and schizophrenic patients.9 This study lent further credence to our hypothesis that frontal lobe imbalance could be addressed either by excitation of the hypofunctioning cortex or suppression of its contralateral homologue. This study was conducted to validate this concept in a pilot study of normal subjects and depressed patients who underwent an identical right frontal lobe SF r-TMS experimental protocol.


Eight otherwise healthy persons who met DSM-IV clinical criteria for dysthymia or unipolar depression without psychotic features and six healthy controls completed the protocol. Both groups were instructed to abstain from any mood altering substances or medications except those prescribed. Depressed patients were given the option of adjunctive medical therapy. Our psychiatrist (PB) administered the Hamilton-D and Beck depression inventory scales before and within 2 weeks after the TMS protocol. Motor threshold was determined as the percentage output of a Cadwell MES-10 stimulator that produced an identical motor evoked potential elicited in the dominant hand in three of six consecutive trials. The right dorsal frontal lobe was located by mirroring the technique of Pascual-Leone.10 Each right frontal lobe stimulation session consisted of five sets of 20 stimuli given at 0.5 Hz separated by a 1 minute rest period at motor threshold. All subjects underwent eight sessions within a 6 week period with no more than 1 week between treatments and never more than two treatments a week.

Statistical analysis was performed by a statistician blinded to the hypothesis. Normally distributed data were analysed with at test. Non-normally distributed data were assessed with the non-parametric Mann-WhitneyU test. A one way analysis of variance (ANOVA) test was used to reject the null hypothesis that the improvement in the depressed patients could be attributed solely to the effects of time.


No significant differences were noted between the control and depressed groups with respect to age, sex, threshold, or handedness (p>0.05). These data are summarised in the table. No depressed patient reported any adverse effects. Two controls reported one episode of a transient tension headache. One female subject in each group was excluded for protocol violation. The control later admitted to a history of depression whereas the experimental subject became pregnant.

Summary of results

The study entry scores were significantly different between the normal and depressed groups on both rating scales (p<0.01). No changes were noted in the normal subjects between study entry and completion scores on either scale (p>0.05). An ANOVA test on the depressed patients’ scores was able to reject the null hypothesis that the improvement was due solely to time (p>0.05). The depressed patients showed a statistically significant improvement on both scales; Beck depression inventory (p<0.05) and Hamilton-D (p<0.02). Four depressed patients requested adjunctive medical therapy with selective serotonin reuptake inhibitors (three used paroxetine, one used sertraline). One person using paroxetine was also given adjunctive treatment with imipramine. When depressed subgroup analysis of patients was undertaken, the TMS alone group had a marginal but insignificant trend of greater improvement (p>0.05). For all depressed patients, there was a significant difference between the Beck depression inventory and Hamilton-D scores before and after the treatment (p<0.05).


This study shows a statistically significant antidepressant effect of right frontal SF r-TMS limited to depressed patients, with no adverse effects in either group. These results support the frontal lobe imbalance paradigm of unipolar depression. Although Hamilton-D scores showed greater statistical significance than the Beck depression inventory, the fact that both scores improved in the same direction suggests a true effect rather than observer bias.

To our knowledge, this is the first controlled antidepressant trial of right frontal SF r-TMS. Unlike the dysphoria reported by controls receiving FF r-TMS, our controls experienced no such adverse effects.11 FF r-TMS may cause greater initial cortical inhibition than SF r-TMS, which may increase the risk of adverse effects. In addition to the lack of adverse effects on controls, SF r-TMS is less expensive, safer, and easier to administer.

Despite these encouraging results, several caveats are in order. All depressed patients were treated on an outpatient basis. As such, the effects of SF r-TMS on severe, psychotic, and bipolar depression are still unknown. This trial did not compare the efficacy of SF r-TMS versus FF r-TMS or ECT. Thus, we concur with previously published recommendations that TMS should neither be employed as a first line treatment for depression nor substituted for electroconvulsive therapy in drug resistant depression.12 An exception might be made for those at high risk for general anaesthesia. Despite these precautions, SF r-TMS may prove to be an alternative treatment for those who are unwilling or unable to undergo medical therapy or electroconvulsive therapy. The results of this study justify further research into this novel and promising technique.


Disclaimer: The views expressed in this article represent those of the authors and should not be construed to represent those of the United States Air Force or the Department of Defense. All subjects who participated in this study gave their voluntary informed consent. All studies were conducted in accordance with local IRB policy and with United States Air Force Instructions concerning research on human subjects.