A randomized controlled trial of a standard 4-week protocol of repetitive transcranial magnetic stimulation in severe treatment resistant depression
Publication year
2020Author(s)
Number of pages
6 p.
Source
Journal of Affective Disorders, 274, (2020), pp. 444-449ISSN
Publication type
Article / Letter to editor

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Organization
Psychiatry
PI Group Memory & Emotion
SW OZ BSI KLP
PI Group Statistical Imaging Neuroscience
SW OZ DCC CO
Journal title
Journal of Affective Disorders
Volume
vol. 274
Languages used
English (eng)
Page start
p. 444
Page end
p. 449
Subject
220 Statistical Imaging Neuroscience; Action, intention, and motor control; All institutes and research themes of the Radboud University Medical Center; Experimental Psychopathology and Treatment; Radboudumc 13: Stress-related disorders DCMN: Donders Center for Medical NeuroscienceAbstract
Background: Treatment options for major depressive disorder (MDD) in individuals who are depressed for at least 2 years and failed two or more different types of therapeutic intervention, remain scarce. Being less invasive than electroconvulsive therapy, repetitive transcranial magnetic stimulation (rTMS) might be an alternative treatment option. Research Question: Does high frequency rTMS applied over the left prefrontal cortex ameliorate depressive symptoms in patients with treatment resistant major depressive disorder and is the efficacy dependent on treatment resistance? Method: We performed a randomized controlled trial investigating the effect of twenty sessions of real or sham-rTMS, during 4 consecutive weeks. Efficacy was blindly rated with the Hamilton depression rating scale (HDRS-17) at baseline and 1 week after end of treatment, and the Dutch method for quantification of treatment resistance in Depression (DM-TRD) was assessed at baseline. Results: An interim analysis showed no differences in antidepressant response between real and sham rTMS and we therefore discontinued the RCT after 31 patients. The mean difference of the HDRS score between baseline and post-treatment was 3.7 (± 4.0; change 16%), indicating a small but significant improvement across time (F(1,30)=25.4;p<0.01). There were no differences however between the treatment arms (F(1.30)=1.5;p=0.23). We did find a negative correlation between the change in HDRS score and DM-TRD in the active rTMS group, but this correlation was not significantly different from the sham group. Conclusion: "Standard" 4-week rTMS treatment is not effective in chronic, severe treatment-resistant depressed patients. While a replication of our data in this patient group may be ethically difficult, further research with less treatment resistant patients might help in positioning rTMS within the current stepped care approach to depression.
This item appears in the following Collection(s)
- Academic publications [232002]
- Donders Centre for Cognitive Neuroimaging [3760]
- Electronic publications [115206]
- Faculty of Medical Sciences [89012]
- Faculty of Social Sciences [29073]
- Open Access publications [82595]
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