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Dissociation and Alterations in Brain Function and Structure: Implications for Borderline Personality Disorder

Annegret Krause-Utz, R. Frost, D. Winter, Bernet M. Elzinga

Current Psychiatry Reports January 30, 2017 DOI: 10.1007/s11920-017-0757-y (opens in new tab)

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Characteristics Review Peer reviewed
Key findings The authors provide an overview of neurobiological models of dissociation based mainly on neuroimaging in depersonalization/derealization disorder, dissociative identity disorder, and the dissociative subtype of PTSD, then review recent studies linking dissociation to altered brain function and structure in borderline personality disorder. They note that such BPD studies remain relatively rare and discuss methodological differences and limitations, along with implications for research and clinical settings.

Abstract

Dissociation involves disruptions of usually integrated functions of consciousness, perception, memory, identity, and affect (e.g., depersonalization, derealization, numbing, amnesia, and analgesia). While the precise neurobiological underpinnings of dissociation remain elusive, neuroimaging studies in disorders, characterized by high dissociation (e.g., depersonalization/derealization disorder (DDD), dissociative identity disorder (DID), dissociative subtype of posttraumatic stress disorder (D-PTSD)), have provided valuable insight into brain alterations possibly underlying dissociation. Neuroimaging studies in borderline personality disorder (BPD), investigating links between altered brain function/structure and dissociation, are still relatively rare. In this article, we provide an overview of neurobiological models of dissociation, primarily based on research in DDD, DID, and D-PTSD. Based on this background, we review recent neuroimaging studies on associations between dissociation and altered brain function and structure in BPD. These studies are discussed in the context of earlier findings regarding methodological differences and limitations and concerning possible implications for future research and the clinical setting.

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