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9.11 - Borderline Personality Disorder

from 9 - Integrated Neurobiology of Specific Syndromes and Treatments

Published online by Cambridge University Press:  08 November 2023

Mary-Ellen Lynall
Affiliation:
University of Cambridge
Peter B. Jones
Affiliation:
University of Cambridge
Stephen M. Stahl
Affiliation:
University of California, San Diego
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Summary

This chapter considers the neuroscience of borderline personality disorder, also known as emotionally unstable personality disorder, focusing on three domains: neuroendocrinological, structural and functional findings. Research in these areas is related to clinical understanding of borderline personality disorder as characterised by (a) emotional dysregulation, (b) impulsivity and (c) social dysfunction. In patients with borderline personality disorder, the hypothalamic–pituitary–adrenal (HPA) axis tends to show showing elevated continuous cortisol output and blunted cortisol following psychosocial challenges. The amygdala and hippocampus differ from healthy controls in terms of both reduced volume and measurable activity, and the dorsolateral prefrontal cortex tends to be less active. The neurobiology of borderline personality disorder can be characterised as a proneness to flooding by cortisol, with the amygdala working to heighten the affective meaning of stressful stimuli, and the prefrontal cortex underperforming in the task of downregulating emotional experience. The chapter also considers genetic findings in relation to borderline personality disorder.

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Chapter
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Publisher: Cambridge University Press
Print publication year: 2023

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References

American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, 5th ed. (DSM-5). American Psychiatric Association, 2013.Google Scholar
Ruocco, A. C., Carcone, D.. A neurobiological model of borderline personality disorder: Systematic and integrative review. Harvard Review of Psychiatry 2016; 24(5): 311329.CrossRefGoogle ScholarPubMed
Thomas, N., Gurvich, C., Hudaib, A.-R., Gavrilidis, E., Kulkarni, J.. Systematic review and meta-analysis of basal cortisol levels in borderline personality disorder compared to non-psychiatric controls. Psychoneuroendocrinology 2019; 102: 149157.CrossRefGoogle ScholarPubMed
Lupien, S., McEwen, B., Gunnar, M., Heim, C. Effects of stress throughout the lifespan on the brain, behaviour and cognition. Nature Reviews Neuroscience 10; 2009: 434445.CrossRefGoogle ScholarPubMed
Drews, E., Fertuck, E. A, Koenig, J., Kaess, M., Arntz, A.. Hypothalamic–pituitary–adrenal axis functioning in borderline personality disorder: a meta-analysis. Neuroscience and Biobehavioral Reviews 2019; 96: 316334.CrossRefGoogle ScholarPubMed
McEwen, B. S. Allostasis and allostatic load: implications for neuropsychopharmacology. Neuropsychopharmacology 2000; 22(2): 108124.CrossRefGoogle ScholarPubMed
Herpertz, S. C., Bertsch, K.. A new perspective on the pathophysiology of borderline personality disorder: a model of the role of oxytocin. American Journal of Psychiatry 2015; 172(9): 840851.CrossRefGoogle Scholar
Xu, L., Becker, B., Kendrick, K. M.. Oxytocin facilitates social learning by promoting conformity to trusted individuals. Frontiers in Neuroscience 2019; 13: 56.CrossRefGoogle ScholarPubMed
Russo, S., Nestler, E. Brain reward circuitry in mood disorders. Nature Reviews Neuroscience 2013; 14:609625.CrossRefGoogle ScholarPubMed
Ruocco, A. C., Amirthavasagam, S., Zakzanis, K. K.. Amygdala and hippocampal volume reductions as candidate endophenotypes for borderline personality disorder: a meta-analysis of magnetic resonance imaging studies. Psychiatry Research: Neuroimaging 2012; 201(3): 245252.CrossRefGoogle ScholarPubMed
Nunes, P. M., Wenzel, A, Tavares Borges, K et al. Volumes of the hippocampus and amygdala in patients with borderline personality disorder: a meta-analysis. Journal of Personality Disorders 2009; 23(4): 333345.CrossRefGoogle ScholarPubMed
Schulze, L., Schmahl, C., Niedtfeld, I.. Neural correlates of disturbed emotion processing in borderline personality disorder: a multimodal meta-analysis. Biological Psychiatry 2016; 79(2): 97106.CrossRefGoogle ScholarPubMed
Stepp, S. D., Lazarus, S. A., Byrd, A. L.. A systematic review of risk factors prospectively associated with borderline personality disorder: taking stock and moving forward. Personality Disorders: Theory, Research, and Treatment 2016; 7(4): 316323.CrossRefGoogle ScholarPubMed
Distel, M. A., Trull, T. J., Derom, C. A. et al. Heritability of borderline personality disorder features is similar across three countries. Psychological Medicine 2008; 38(9): 12191229.CrossRefGoogle ScholarPubMed
Distel, M. A., Middeldorp, C. M., Trull, T. J. et al. Life events and borderline personality features: the influence of gene–environment interaction and gene–environment correlation. Psychological Medicine 2011; 41(4): 849860.CrossRefGoogle ScholarPubMed
Belsky, J. The development of human reproductive strategies: progress and prospects. Current Directions in Psychological Science 2012; 21(5): 310316.CrossRefGoogle Scholar
Macdonald, A. N., Goines, K. B, Novacek, D. M., Walker, E. F.. Prefrontal mechanisms of comorbidity from a transdiagnostic and ontogenic perspective. Development and Psychopathology 2016; 28(4): 11471175.CrossRefGoogle ScholarPubMed
Wise, T., Radua, J., Via, E. et al. Common and distinct patterns of grey-matter volume alteration in major depression and bipolar disorder: evidence from voxel-based meta-analysis. Molecular Psychiatry 2016; 22(10): 14551463.CrossRefGoogle ScholarPubMed
World Health Organization. International Classification of Diseases, 11th ed. (ICD-11). World Health Organization, 2018.Google Scholar
McClure, G., Hawes, D. J., Dadds, M. R.. Borderline personality disorder and neuropsychological measures of executive function: a systematic review. Personality and Mental Health 2016; 10(1): 4357.CrossRefGoogle ScholarPubMed

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