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Oxytocin and Reduction of Social Threat Hypersensitivity in Women With Borderline Personality Disorder

TLDR
Borderline patients exhibit a hypersensitivity to social threat in early, reflexive stages of information processing, and oxytocin may decrease social threat hypersensitivity and thus reduce anger and aggressive behavior in borderline personality disorder or other psychiatric disorders with enhanced threat-driven reactive aggression.
Abstract
Objective: Patients with borderline personality disorder are characterized by emotional hyperarousal with increased stress levels, anger proneness, and hostile, impulsive behaviors. They tend to ascribe anger to ambiguous facial expressions and exhibit enhanced and prolonged reactions in response to threatening social cues, associated with enhanced and prolonged amygdala responses. Because the intranasal administration of the neuropeptide oxytocin has been shown to improve facial recognition and to shift attention away from negative social information, the authors investigated whether borderline patients would benefit from oxytocin administration. Method: In a randomized placebocontrolled double-blind group design, 40 nonmedicated, adult female patients with a current DSM-IV diagnosis of borderline personality disorder (two patients were excluded based on hormonal analyses) and 41 healthy women, matched on age, education, and IQ, took part in an emotion classification task 45 minutes after intranasal administration of 26 IU of oxytocin or placebo. Dependent variables were latencies and number or initial reflexive eye movements measured by eye tracking, manual response latencies, and blood-oxygen-level-dependent responses of theamygdalato angryandfearfulcompared with happy facial expressions. Results: Borderline patients exhibited more and faster initial fixation changes to the eyes of angry faces combined with increased amygdala activation in response to angry faces compared with the control group. These abnormal behavioral and neural patterns were normalized after oxytocin administration. Conclusions: Borderline patients exhibit a hypersensitivity to social threat in early, reflexive stages of information processing. Oxytocin may decrease social threat hypersensitivity and thus reduce anger and aggressive behavior in borderline personality disorder or other psychiatric disorders with enhanced threat-driven reactive aggression. (Am J Psychiatry 2013; 170:1169–1177)

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A Neuroscience-Oriented Research Approach to Borderline Personality Disorder.

TL;DR: It is suggested that linking the underlying neurobiological abnormalities to behavioral symptoms of the disorder can inform a research agenda to better understand BPD with its multiple presentations.
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Emotion avoidance and fear bradycardia in patients with borderline personality disorder and healthy controls

TL;DR: The results may suggest impaired automatic defense responses in BPD, and further understanding of the regulation of distress and defense responses might improve BPD treatment.
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Oxytocin release deficit and social cognition in craniopharyngioma patients.

TL;DR: The findings suggest that reduced emotional processing abilities may represent a pathological feature in a group of craniopharyngioma patients, indicating that this patient group might benefit from specific treatments within the social domain.
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Atypical processing of social anticipation and feedback in borderline personality disorder

TL;DR: Borderline personality disorder (BPD) is characterized by interpersonal dysfunction, and the superior temporal sulcus is hyperactivated during social anticipation and amygdala response to evaluative social feedback is reduced.
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Oxytocin and callous-unemotional traits: towards a social-cognitive approach to forensic analysis

TL;DR: The hypothesis that the administration of exogenous oxytocin is a biological intervention worthy of further investigation to address Callous-unemotional traits and moderate future risk factors for forensic behaviors is advanced.
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Oxytocin Modulates Neural Circuitry for Social Cognition and Fear in Humans

TL;DR: It is shown that human amygdala function is strongly modulated by oxytocin, and this results indicate a neural mechanism for the effects of Oxytocin in social cognition in the human brain and provide a methodology and rationale for exploring therapeutic strategies in disorders in which abnormal amygdala function has been implicated, such as social phobia or autism.
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Oxytocin and vasopressin in the human brain: social neuropeptides for translational medicine

TL;DR: OXT and AVP are emerging as targets for novel treatment approaches — particularly in synergistic combination with psychotherapy — for mental disorders characterized by social dysfunction, such as autism, social anxiety disorder, borderline personality disorder and schizophrenia.
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