Affiliation:
1. Charité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin,
Klinik für Psychiatrie und Psychotherapie, Campus Benjamin Franklin, Berlin, Germany
Abstract
Abstract:
Borderline personality disorder (BPD) is characterized by emotional instability, impulsivity
and unstable interpersonal relationships. Patients experience discomforting levels of distress, inducing
symptoms like dissociation, aggression or withdrawal. Social situations are particularly challenging,
and acute social stress can reduce patients’ cognitive and social functioning. In patients with Major
Depressive Disorder or Posttraumatic Stress Disorder, which show high comorbidity with BPD, the
endocrine stress response is characterized by Hypothalamus-Pituitary-Adrenal (HPA) axis dysfunction,
which affects cognitive functioning. Compared to these clinical groups, research on HPA-axis
function in BPD is relatively scarce, but evidence points towards a blunted cortisol reactivity to acute
stress. Since BPD patients are particularly prone to social stress and experience high subjective difficulties
in these situations, it seems plausible that HPA-axis dysregulation might contribute to decreased
social cognition in BPD. The present review summarizes findings on the HPA-axis function in
BPD and its association with social cognition following acute social stress. For this purpose, we review
literature that employed a widely used social stressor (Trier Social Stress Test, TSST) to study
the effects of acute social stress on social cognition and the HPA-axis response. We contrast these
findings with studies on social cognition that employed Cyberball, another widely used social stressor
that lacks HPA-axis involvement. We conclude that research on social cognition in BPD reveals heterogeneous
results with no clear relationship between social functioning and HPA-axis response. More
research is needed to better understand the psychophysiological underpinnings of impaired social cognition
in BPD.
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology (medical),Psychiatry and Mental health,Neurology (clinical),Neurology,Pharmacology,General Medicine
Cited by
2 articles.
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