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Abstract
Theta-burst stimulation (TBS) represents a brain stimulation technique effective for treatment-resistant depression (TRD) as underlined by meta-analyses. While the methodology undergoes constant refinement, bilateral stimulation of the dorsolateral prefrontal cortex (DLPFC) appears promising to restore left DLPFC hypoactivity and right hyperactivity found in depression. The post-synaptic inhibitory serotonin-1A (5-HT1A) receptor, also occurring in the DLPFC, might be involved in this mechanism of action. To test this hypothesis, we performed PET-imaging using the tracer [carbonyl-11C]WAY-100635 including arterial blood sampling before and after a three-week treatment with TBS in 11 TRD patients compared to sham stimulation (n = 8 and n = 3, respectively). Treatment groups were randomly assigned, and TBS protocol consisted of excitatory intermittent TBS to the left and inhibitory continuous TBS to the right DLPFC. A linear mixed model including group, hemisphere, time, and Hamilton Rating Scale for Depression (HAMD) score revealed a 3-way interaction effect of group, time, and HAMD on specific distribution volume (VS) of 5-HT1A receptor. While post-hoc comparisons showed no significant changes of 5-HT1A receptor VS in either group, higher 5-HT1A receptor VS after treatment correlated with greater difference in HAMD (r = −0.62). The results of this proof-of-concept trial hint towards potential effects of TBS on the distribution of the 5-HT1A receptor. Due to the small sample size, all results must, however, be regarded with caution.
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1 Medical University of Vienna, Department of Psychiatry and Psychotherapy, Clinical Division of General Psychiatry, Vienna, Austria (GRID:grid.22937.3d) (ISNI:0000 0000 9259 8492); Medical University of Vienna, Comprehensive Center for Clinical Neurosciences and Mental Health, Vienna, Austria (GRID:grid.22937.3d) (ISNI:0000 0000 9259 8492)
2 Medical University of Vienna, Department of Biomedical Imaging and Image-guided Therapy, Division of Nuclear Medicine, Vienna, Austria (GRID:grid.22937.3d) (ISNI:0000 0000 9259 8492)
3 Medical University of Vienna, Department of Psychiatry and Psychotherapy, Clinical Division of General Psychiatry, Vienna, Austria (GRID:grid.22937.3d) (ISNI:0000 0000 9259 8492); The Hong Kong Polytechnic University, Department of Rehabilitation Sciences, Hung Hom, Hong Kong (GRID:grid.16890.36) (ISNI:0000 0004 1764 6123)
4 Medical University of Vienna, Department of Biomedical Imaging and Image-guided Therapy, Division of Nuclear Medicine, Vienna, Austria (GRID:grid.22937.3d) (ISNI:0000 0000 9259 8492); Ludwig Boltzmann Institute Applied Diagnostics, Vienna, Austria (GRID:grid.511291.f); University of Vienna, Department of Chemistry, Institute of Inorganic Chemistry, Vienna, Austria (GRID:grid.10420.37) (ISNI:0000 0001 2286 1424)
5 Medical University of Vienna, Department of Psychiatry and Psychotherapy, Clinical Division of General Psychiatry, Vienna, Austria (GRID:grid.22937.3d) (ISNI:0000 0000 9259 8492)