Clinical effects of glabellar botulinum toxin injections on borderline personality disorder: A randomized controlled trial

Author:

Wollmer M Axel1,Neumann Insa1ORCID,Jung Stefanie2,Bechinie Agnès2,Herrmann Julian2,Müller Antje1,Wohlmuth Peter3,Fournier-Kaiser Larissa1,Sperling Christian2,Peters Liza1,Kneer Jonas2,Engel Jannis2,Jürgensen Frank1,Schulze Jara2,Nagel Matthias45,Prager Welf6,Sinke Christopher2,Kahl Kai G7,Karst Matthias8,Dulz Birger1,Kruger Tillmann H C29

Affiliation:

1. Asklepios Clinic North - Ochsenzoll, Asklepios Campus Hamburg, Medical Faculty, Semmelweis University, Germany

2. Department of Psychiatry, Social Psychiatry and Psychotherapy, Division of Clinical Psychology and Sexual Medicine, Hannover Medical School, Hannover, Germany

3. Asklepios Proresearch, Hamburg, Germany

4. Department of Psychiatry and Psychotherapy, Asklepios Clinic North – Wandsbek, Hamburg, Germany

5. Clinic for Psychiatry and Psychotherapy, University of Lübeck, Luebeck, Germany

6. Dermatologische Praxis, Prager & Partner, Hamburg, Germany

7. Department of Psychiatry, Social Psychiatry and Psychotherapy, Hannover Medical School, Hannover, Germany

8. Department of Anesthesiology and Intensive Care Medicine, Pain Clinic, Hannover Medical School, Hannover, Germany

9. Center for Systems Neuroscience, Hannover, Germany

Abstract

Background: Inhibition of frowning via injections of botulinum toxin A (BTX) into the glabellar region has shown beneficial effects in the treatment of major depression. Preliminary research suggests that improvements in the affective domain are not depression-specific, but may also translate to other psychiatric disorders. Aim: This 16-week, single-blind, two-center randomized controlled trial investigated the influence of BTX on clinical symptoms of borderline personality disorder (BPD). Methods: Fifty-four patients with BPD were randomly assigned to treatment with BTX (n = 27) or a minimal acupuncture (ACU) control condition ( n = 27). Clinical outcomes were followed at 2, 4, 6, 8, 12, and 16 weeks. Primary endpoint was the relative score change on the Zanarini Rating Scale for Borderline Personality Disorder (ZAN-BPD) 8 weeks after baseline relative to the control group and adjusted for treatment center. Secondary and additional outcome variables were self-rated borderline symptoms, comorbid symptoms of depression, psychological distress, and clinical global impression. Results: Participants showed significant improvements at the primary efficacy endpoint in both treatment groups (BTX: M = −0.39, SD = 0.39; ACU: M = −0.35, SD = 0.42), but no superior effect of the BTX condition in comparison with the control intervention was found— F(1,5323) = 0.017, p = 0.68). None of the secondary or additional outcomes yielded significant group differences. Side effects were mild and included headache, transient skin or muscle irritations, and dizziness. Conclusion: Evidence regarding the efficacy of BTX for BDP remains limited, and the design of adequate control conditions presents an opportunity for further research. ClinicalTrials.gov registry: Botulinum Toxin A for Emotional Stabilization in Borderline Personality Disorder (BPD), NCT02728778, https://clinicaltrials.gov/ct2/show/NCT02728778

Publisher

SAGE Publications

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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