Exploring nonverbal synchrony in borderline personality disorder: A double-blind placebo-controlled study using oxytocin.

borderline personality disorder motion energy analysis (MEA) nonverbal behaviour nonverbal synchrony oxytocin rejection sensitivity

Journal

The British journal of clinical psychology
ISSN: 0144-6657
Titre abrégé: Br J Clin Psychol
Pays: England
ID NLM: 8105533

Informations de publication

Date de publication:
Jun 2020
Historique:
received: 19 02 2019
revised: 27 06 2019
pubmed: 28 11 2019
medline: 14 7 2020
entrez: 28 11 2019
Statut: ppublish

Résumé

Interpersonal dysfunction is a central feature of borderline personality disorder (BPD), and the neuropeptide oxytocin (OT) has been shown to impact patients' behaviour in numerous ways. Nonverbal signals such as the coordination of body movement (nonverbal synchrony) are associated with the success of interpersonal exchanges and could thus be influenced by features of BPD and by the administration of OT. We explored the effect of intranasal OT (inOT) on nonverbal synchrony in sixteen patients with BPD and fifteen healthy controls (CTL) randomly assigned to two double-blind clinical interviews under inOT and placebo (PL). Nonverbal synchrony was assessed by automated video-analyses of subject's and interviewer's body movement. Lagged cross-correlations were used to objectively quantify coordination in dyads. Synchrony was higher than pseudosynchrony (= synchrony expected by chance), and there was a differential effect of inOT between groups: While healthy controls displayed increased synchrony under inOT, patients with BPD showed low levels of synchrony under inOT. Additionally, patient's synchrony was negatively associated with self-reported childhood trauma. Nonverbal synchrony in clinical interviews is influenced by inOT, and this effect depends on subject's diagnosis. In line with previous research implying positive associations between nonverbal synchrony and relationship quality, inOT led to an increase of synchrony in healthy controls, but not in patients with BPD. Low levels of synchrony under inOT in patients and its association with childhood trauma suggest that additional mechanisms such as rejection sensitivity might mediate BPD patients' nonverbal behaviour. Intranasal oxytocin (inOT) attenuated nonverbal synchrony - a proxy for relationship quality - in patients with borderline personality disorder (BPD), while it increased nonverbal synchrony in healthy controls (CTL). Available models (rejection sensitivity; social salience) suggest that inOT may alter the way patients with BPD assess social situations, and this alteration is expressed by changes in nonverbal coordination. Patients with BPD display low levels of synchrony which are even below expected pseudosynchrony based on chance. The association between self-reported childhood trauma and lower synchrony in BPD was most evident for patient's imitative behaviour: Under inOT, patients with high scores of childhood trauma refrained from imitating their interview partners. Study limitations include small sample sizes and limited data on the psychological impact of the clinical interviews.

Identifiants

pubmed: 31774581
doi: 10.1111/bjc.12240
doi:

Substances chimiques

Oxytocics 0
Oxytocin 50-56-6

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

186-207

Informations de copyright

© 2019 The Authors. British Journal of Clinical Psychology published by John Wiley & Sons Ltd on behalf of British Psychological Society.

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Auteurs

Fabian Ramseyer (F)

Department of Clinical Psychology and Psychotherapy, Institute of Psychology, University of Bern, Switzerland.

Andreas Ebert (A)

Division of Social Neuropsychiatry and Evolutionary Medicine, Department of Psychiatry, Psychotherapy and Preventive Medicine, LWL University Hospital Bochum, Ruhr-University Bochum, Germany.

Patrik Roser (P)

Centre for Addiction Disorders, Psychiatric Hospital Königsfelden, Psychiatric Services Aargau, Academic Hospital of the University of Zurich, Switzerland.

Marc-Andreas Edel (MA)

Fliedner Klinic, Gevelsberg, Germany.

Wolfgang Tschacher (W)

Department of Experimental Psychology, University Hospital of Psychiatry and Psychotherapy, University of Bern, Switzerland.

Martin Brüne (M)

Division of Social Neuropsychiatry and Evolutionary Medicine, Department of Psychiatry, Psychotherapy and Preventive Medicine, LWL University Hospital Bochum, Ruhr-University Bochum, Germany.

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