BRAIN STIMULATION: Basic, Translational, and Clinical Research in Neuromodulation
Volume 4, Issue 4 , Pages 266-274, October 2011

Differential effects of deep TMS of the prefrontal cortex on apathy and depression

  • Yechiel Levkovitz

      Affiliations

    • Cognitive and Emotional Laboratory, Shalvata Mental Health Care Center, Hod-Hasharon, Israel
  • ,
  • Aharon Sheer

      Affiliations

    • Weizmann Institute of Science, Neurobiology Department, Rehovot 76100, Israel
  • ,
  • Eiran V. Harel

      Affiliations

    • Cognitive and Emotional Laboratory, Shalvata Mental Health Care Center, Hod-Hasharon, Israel
  • ,
  • Leor N. Katz

      Affiliations

    • Weizmann Institute of Science, Neurobiology Department, Rehovot 76100, Israel
  • ,
  • Dana Most

      Affiliations

    • Weizmann Institute of Science, Neurobiology Department, Rehovot 76100, Israel
  • ,
  • Abraham Zangen

      Affiliations

    • Weizmann Institute of Science, Neurobiology Department, Rehovot 76100, Israel
  • ,
  • Moshe Isserles

      Affiliations

    • Department of Psychiatry, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
    • Corresponding Author InformationCorrespondence: Dr. Moshe Isserles, Department of Psychiatry, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.

Received 31 May 2010; received in revised form 21 December 2010; accepted 21 December 2010. published online 25 January 2011.

Background

Apathy is one hallmark of major depression (MDD). It is distinguished by lack of emotion, whereas other aspects of depression involve considerable emotional distress. Investigating both apathy and depression may increase the degree of treatment efficacy for both ailments together and apart.

Objective

Evaluate the differential effects of deep transcranial magnetic stimulation (DTMS) over the prefrontal cortex (PFC) on apathy and other aspects of depression in patients suffering from a depressive episode.

Methods

Fifty-four treatment-resistant MDD patients were evaluated with the Hamilton Rating Scale for Depression (HRSD), and then treated with DTMS. Apathy-related items from HRSD (ApHRSD) were compared with the remaining items from HRSD (DepHRSD). Antidepressant medications were withdrawn and active DTMS treatment was administered at 20 Hz, 5 days a week for 4 weeks. Changes in HRSD were recorded. Primary efficacy time point was 1 week after the end of active treatment.

Results

At screening, ApHRSD distribution was unimodal (moderate apathy), with low correlation (r = 0.17) between ApHRSD and DepHRSD. After treatment, a third had remitted apathy, and the correlation between ApHRSD and DepHRSD had dramatically increased (r = 0.83). Severe ApHRSD (≥ 7) at screening correlated with nonremission for both ApHRSD (R2 = 0.1993, P = .0012) and DepHRSD (R2 = 0.0860, P = .0334).

Conclusions

DTMS over the PFC improved both apathy and depression similarly. However, DTMS did not lead to MDD remission if ApHRSD at screening was ≥ 7 of 12. Further investigation using a larger sample will determine whether screening apathy at baseline could be used to predict efficacy of DTMS in MDD patients.

Keywords: MDD, treatment-resistant, DTMS, H-coil, ApHRSD, DSM-V

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 This study was supported by the Rosenzweig-Coopersmith Fund and Brainsway Inc.

 Drs. Levkovitz and Zangen are consultants for and have financial interests in Brainsway Inc., which has commercial interests in the development of deep TMS coils. Dr. Isserles receives financial support from Brainsway Inc.

 Yechiel Levkovitz and Aharon Sheer contributed equally to this work.

PII: S1935-861X(10)00206-8

doi:10.1016/j.brs.2010.12.004

BRAIN STIMULATION: Basic, Translational, and Clinical Research in Neuromodulation
Volume 4, Issue 4 , Pages 266-274, October 2011