Borderline personality disorder: associations with psychiatric disorders, somatic illnesses, trauma, and adverse behaviors.


Journal

Molecular psychiatry
ISSN: 1476-5578
Titre abrégé: Mol Psychiatry
Pays: England
ID NLM: 9607835

Informations de publication

Date de publication:
05 2022
Historique:
received: 16 07 2021
accepted: 22 02 2022
revised: 01 02 2022
pubmed: 20 3 2022
medline: 31 5 2022
entrez: 19 3 2022
Statut: ppublish

Résumé

In one of the largest, most comprehensive studies on borderline personality disorder (BPD) to date, this article places into context associations between this diagnosis and (1) 16 different psychiatric disorders, (2) eight somatic illnesses, and (3) six trauma and adverse behaviors, e.g., violent crime victimization and self-harm. Second, it examines the sex differences in individuals with BPD and their siblings. A total of 1,969,839 Swedish individuals were identified from national registers. Cumulative incidence with 95% confidence intervals (CI) was evaluated after 5 years of follow-up from BPD diagnosis and compared with a matched cohort. Associations were estimated as hazard ratios (HR) with 95% CIs from Cox regression. 12,175 individuals were diagnosed with BPD (85.3% female). Individuals diagnosed with BPD had higher cumulative incidences and HRs for nearly all analyzed indicators, especially psychiatric disorders. Anxiety disorders were most common (cumulative incidence 95% CI 33.13% [31.48-34.73]). Other notable findings from Cox regressions include psychotic disorders (HR 95% CI 24.48 [23.14-25.90]), epilepsy (3.38 [3.08-3.70]), violent crime victimization (7.65 [7.25-8.06]), and self-harm (17.72 [17.27-18.19]). HRs in males and females with BPD had overlapping CIs for nearly all indicators. This indicates that a BPD diagnosis is a marker of vulnerability for negative events and poor physical and mental health similarly for both males and females. Having a sibling with BPD was associated with an increased risk for psychiatric disorders, trauma, and adverse behaviors but not somatic disorders. Clinical implications include the need for increased support for patients with BPD navigating the health care system.

Identifiants

pubmed: 35304564
doi: 10.1038/s41380-022-01503-z
pii: 10.1038/s41380-022-01503-z
pmc: PMC9135625
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

2514-2521

Subventions

Organisme : NIMH NIH HHS
ID : R01 MH123724
Pays : United States

Informations de copyright

© 2022. The Author(s).

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Auteurs

Ashley E Tate (AE)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden. Ashley.tate@ki.se.

Hanna Sahlin (H)

Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.

Shengxin Liu (S)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden.

Yi Lu (Y)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden.

Sebastian Lundström (S)

Centre for Ethics, Law and Mental Health (CELAM), University of Gothenburg, Gothenburg, Sweden.
Gillberg Neuropsychiatry Centre, University of Gothenburg, Gothenburg, Sweden.

Henrik Larsson (H)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden.
School of Medical Sciences, Örebro University, Örebro, Sweden.

Paul Lichtenstein (P)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden.

Ralf Kuja-Halkola (R)

Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Solna, Sweden.

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