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Exploratory meta-analysis on deep brain stimulation in treatment-resistant depression

Smith DF. Exploratory meta-analysis on deep brain stimulation in treatment-resistant depression.

Published online by Cambridge University Press:  18 September 2013

Donald F. Smith*
Affiliation:
Institute for Clinical Medicine, Translational Neuropsychiatry Unit, Psychiatric Hospital of Aarhus University, Risskov, Denmark
*
Donald F. Smith, Institute for Clinical Medicine, Translational Neuropsychiatry Unit, Psychiatric Hospital of Aarhus University, Risskov, Denmark. Tel: +45-78463026; Fax: +45-78461662;E-mail: [email protected]
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Abstract

Objective

Deep brain stimulation is currently an experimental treatment for major depressive disorder. Information is lacking, however, on how sham responding may affect efficacy. This article applies exploratory meta-analysis to address that topic.

Methods

Data on benefits of deep brain electrical stimulation come from a recent review. Stimulated brain regions included subgenual cingulate, capsular interna, nucleus accumbens, and medial forebrain bundle. Expert opinion plus random number software was used to generate hypothetical values for sham responding.

Results

An effect size of 1.71 (95% CI: 1.47–1.96) was obtained for deep brain stimulation versus sham treatment in patients suffering from long-term treatment-resistant depression.

Conclusion

Preliminary findings on deep brain electrical stimulation suggest that the procedure may be 71% more effective than sham treatment. Expressing these findings as patients-needed-to-treat, deep brain electrical stimulation is required by 2.9 patients with long-term treatment-resistant depression in order for one of them to benefit.

Type
Short Communication
Creative Commons
Creative Common License - CCCreative Common License - BY
This is an Open Access article, distributed under the terms of the Creative Commons Attribution licence (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted re-use, distribution, and reproduction in any medium, provided the original work is properly cited.
Copyright
© Scandinavian College of Neuropsychopharmacology 2014

Significant outcomes

  • This exploratory meta-analysis showed a statistically significant effect in favour of deep brain stimulation in treatment-resistant major depressive disorder.

  • In terms of patients-needed-to-treat, the results show that one out of three patients with long-term treatment-resistant depression can be expected to benefit from deep brain electrical stimulation.

Limitation

  • Estimates of sham responding to deep brain stimulation are derived by expert opinion rather than by properly controlled clinical trials.

Introduction

Direct electrical stimulation in the brain continues to attract much attention for relief of treatment-resistant depression (Reference Berlim, Mcgirr, Van Den Eynde, Fleck and Giacobbe1,Reference Schlaepfer, Bewernick, Kayser, Hurlemann and Coenen2). There is, however, still great uncertainty concerning efficacy, due in part to lack of information on sham responding to the intensive selection and surgical procedures (Reference Blumberger, Mulsant and Daskalakis3). In the absence of such information, we cannot establish the likelihood of success of the intervention. There are, however, ways of estimating the likelihood of sham responding in certain situations (Reference Merkl, Schneider and Schonecker4). Here, expert opinion is applied to gain an understanding of the potential role of sham responding in the efficacy of deep brain stimulation in patients suffering from long-term treatment-resistant depression.

Materials and methods

Information on the likelihood of sham responding in patients with long-term treatment-resistant depression was solicited from three eminent colleagues (Helen Mayberg, Donald A. Malone Jr., and Thomas E. Schlaepfer) with extended experience using deep brain stimulation for psychiatric disorders (Reference Mayberg, Lozano and Voon5Reference Schlaepfer, Cohen and Frick7). The information that they supplied along with the present authors’ understanding of treatment-resistant depression (Reference Smith, Stork and Wegener8) placed the likelihood of sham responding in the range 10–25%. Using random number software (http://www.random.org/integers/), nine values were generated and were applied consecutively to the data provided by a recent review on deep brain stimulation in long-term treatment-resistant depression (Table 1) (Reference Schlaepfer, Bewernick, Kayser, Hurlemann and Coenen2).

Table 1 Summary of data used for an exploratory meta-analysis on benefit of deep brain electrical stimulation in patients with long-term treatment-resistant depression

The information in the first three columns is summarised from a very recent review (Reference Schlaepfer, Bewernick, Kayser, Hurlemann and Coenen2). The estimates of sham response were obtained by expert opinion plus random number software (http://www.random.org/integers/) (see ‘Materials and methods’ section).

Results

Effect sizes were too heterogeneous to uphold a fixed effects model (Q=36.2, df=7, p<0.01) (Reference Lipsey and Wilson9). Therefore, a random effects model was used, and it provided an estimate of effect size of 1.71 (95% CI: 1.47–1.96; Z=13.6, df=7, p<0.01) for deep brain stimulation versus sham treatment in patients with long-term treatment-resistant depression. In the present context, an effect size of 1.71 means that deep brain stimulation was 71% more likely than sham treatment to be of benefit for patients with long-term treatment-resistant depression.

Discussion

The present exploratory finding can be expressed in terms of patients-needed-to-treat (Reference Connolly and Thase10). Assuming a sham response rate of 20% to the intensive selection and surgical procedures required by deep brain stimulation, then we can expect 2 out of 10 patients to report some benefit even in the absence of electrical stimulation. The estimate of effect size derived by the present exploratory meta-analysis indicates that, in addition to sham responding, another 1.4 patients (i.e. sham response×0.71) can be expected to benefit from electrical stimulation. Thus, for every 2.9 patients (10/3.4) with long-term treatment-resistant depression receiving deep brain electrical stimulation, one can be expected to benefit. Whether this level for patients-needed-to-treat is viewed as large or small is, of course, a matter of opinion.

A shortcoming of the present analysis relates to the current lack of empirical evidence on the level of sham responding to deep brain non-stimulation in patients with long-term treatment-resistant depression. Information on that topic can be expected to come eventually from properly controlled, large-scale clinical trials that either disprove or confirm the present findings. One reviewer of this article noted that two presentations at recent conferences concerned as yet unpublished accounts on clinical trials on deep brain stimulation that were discontinued owing to no difference between active versus sham treatment in depressed subjects. Be that as it may, at least 10 additional clinical trials on deep brain stimulation in depressed subjects are currently underway, according to records available at clinicaltrials.gov. Perhaps the outcome of those studies, once published, can provide further insight concerning the ultimate value of sham versus active deep brain stimulation in treatment-resistant depression.

Acknowledgements

The author thanks Chief Physicist Søren B. Hansen for helpful comments. Helen Mayberg, Donald A. Malone Jr., and Thomas E. Schlaepfer have been informed about the content of this article. The author declares no conflict of interest. This work was done during the author’s employment at Aarhus University.

References

1.Berlim, MT, Mcgirr, A, Van Den Eynde, F, Fleck, MP, Giacobbe, P. Effectiveness and acceptability of deep brain stimulation (DBS) of the subgenual cingulate cortex for treatment-resistant depression: a systematic review and exploratory meta-analysis. J Affect Disord 2014;159:3138.Google Scholar
2.Schlaepfer, TE, Bewernick, BH, Kayser, S, Hurlemann, R, Coenen, VA. Deep brain stimulation of the human reward system for major depression-rationale, outcomes and outlook. Neuropsychopharmacology 2014;39:13031314.CrossRefGoogle ScholarPubMed
3.Blumberger, DM, Mulsant, BH, Daskalakis, ZJ. What is the role of brain stimulation therapies in the treatment of depression? Curr Psychiatry Rep 2013;15:368378.Google Scholar
4.Merkl, A, Schneider, GH, Schonecker, Tet al. Antidepressant effects after short-term and chronic stimulation of the subgenual cingulate gyrus in treatment-resistant depression. Exp Neurol 2013;249:160168.Google Scholar
5.Mayberg, HS, Lozano, AM, Voon, Vet al. Deep brain stimulation for treatment-resistant depression. Neuron 2005;45:651660.Google Scholar
6.Malone, DA Jr. Use of deep brain stimulation in treatment-resistant depression. Cleve Clin J Med 2010;77(Suppl. 3):S77S80.CrossRefGoogle ScholarPubMed
7.Schlaepfer, TE, Cohen, MX, Frick, Cet al. Deep brain stimulation to reward circuitry alleviates anhedonia in refractory major depression. Neuropsychopharmacology 2008;33:368377.Google Scholar
8.Smith, DF, Stork, BS, Wegener, Get al. [11C]Mirtazapine binding in depressed antidepressant nonresponders studied by PET neuroimaging. Psychopharmacology (Berl) 2009;206:133140.CrossRefGoogle ScholarPubMed
9.Lipsey, MW, Wilson, DB. Practical meta-analysis. Thousand Oaks, CA: Sage Publications Inc., 2001.Google Scholar
10.Connolly, KR, Thase, ME. If at first you don’t succeed: a review of the evidence for antidepressant augmentation, combination and switching strategies. Drugs 2011;71:4364.Google Scholar
11.Kennedy, SH, Giacobbe, P, Rizvi, SJet al. Deep brain stimulation for treatment-resistant depression: follow-up after 3 to 6 years. Am J Psychiatry 2011;168:502510.CrossRefGoogle ScholarPubMed
12.Puigdemont, D, Perez-Egea, R, Portella, MJet al. Deep brain stimulation of the subcallosal cingulate gyrus: further evidence in treatment-resistant major depression. Int J Neuropsychopharmacol 2012;15:121133.CrossRefGoogle ScholarPubMed
13.Holtzheimer, PE, Kelley, ME, Gross, REet al. Subcallosal cingulate deep brain stimulation for treatment-resistant unipolar and bipolar depression. Arch Gen Psychiatry 2012;69:150158.CrossRefGoogle ScholarPubMed
14.Lozano, AM, Giacobbe, P, Hamani, Cet al. A multicenter pilot study of subcallosal cingulate area deep brain stimulation for treatment-resistant depression. J Neurosurg 2012;116:315322.Google Scholar
15.Dougherty, DD, Carpenter, LL, Bhati, MTet al. A randomized sham-controlled trial of DBS of the VC/VS for treatment-resistant depression. 67th Annual Scientific Convention, Society of Biological Psychiatry, Philadelphia, PA. 2012.Google Scholar
16.Bewernick, BH, Kayser, S, Sturm, V, Schlaepfer, TE. Long-term effects of nucleus accumbens deep brain stimulation in treatment-resistant depression: evidence for sustained efficacy. Neuropsychopharmacology 2012;37:19751985.Google Scholar
17.Schlaepfer, TE, Bewernick, BH, Kayser, S, Madler, B, Coenen, VA. Rapid effects of deep brain stimulation for treatment-resistant major depression. Biol Psychiatry 2013;73:12041212.Google Scholar
Figure 0

Table 1 Summary of data used for an exploratory meta-analysis on benefit of deep brain electrical stimulation in patients with long-term treatment-resistant depression