Personality Disorder (2025)

Continuing Education Activity

Personality disorders reflect an enduring pattern of inner experience and behavior that deviates markedly from the norms and expectations of the surrounding culture. Individuals with personality disorders may experience distorted perceptions of reality and abnormal affective responses. The diagnosis of a personality disorder is made using criteria described in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5-TR). These disorders can adversely affect multiple aspects of life, including relationships, work, and overall functioning—underscoring the need for early intervention and interdisciplinary care. Early diagnosis and treatment are crucial in managing the symptoms and improving the quality of life for those affected.

Participants in this course gain comprehensive knowledge on the evaluation and management of personality disorders. The course covers the criteria for diagnosis outlined in the DSM-5-TR, various therapeutic approaches, and the importance of early intervention. Emphasizing the role of the multidisciplinary team, the course illustrates how collaboration among mental health professionals, primary care providers, social workers, and other specialists enhances patient outcomes. Effective communication and coordinated care plans ensure that patients receive holistic treatment, addressing both the psychological and social aspects of personality disorders.

Objectives:

  • Assess the impact of personality disorders on a patient's functioning and quality of life through a comprehensive evaluation.

  • Implement evidence-based therapeutic interventions tailored to specific personality disorders to optimize patient care.

  • Evaluate the available evidence for therapeutic interventions for personality disorders to effectively develop and implement an interdisciplinary treatment plan.

  • Collaborate with interdisciplinary team members, including psychologists, psychiatrists, social workers, psychiatric-mental health nurse practitioners, psychiatric nurses, and primary care practitioners, to provide efficient, comprehensive, and coordinated care for patients with a personality disorder.

Access free multiple choice questions on this topic.

Introduction

Temperament classification dates back to ancient Greece when Hippocrates proposed his humoral theory regarding the classifications of behavior. The postulated temperaments, consisting of sanguine, choleric, melancholic, and phlegmatic,remained in use as recently as the 20th century.[1]Emil Kraepelin classified manic-depressive patients as depressive, hypomanic, or irritable, which in turn correlated with melancholic, sanguine, or choleric dispositions.[2] Temperament classifications evolved into the 7 personality disturbances in theDiagnostic and Statistical Manual of Mental Disorders, First Edition(DSM-I), in 1952. The DSM-II (1968) was heavily influenced by psychoanalysis and separated personality disruptions from neuroses of the same name. Over the next 3 decades, psychiatric conceptualizations of personality disorders shifted away from the psychoanalytic model to a categorical model correlating with the medical model originally proposed by Kraepelin. This model was represented by the 11 personality disorders listedin theDSM-III (1980). Current diagnostic criteria sets were introduced in theDSM-IV (1994), with 10personality disorders divided into 3 clusters.[3]

During the production of DSM-5 (2013), editors considered combining a dimensional 5-factor model of behavior with the existing psychoanalytic typological models of personality. Ultimately, the categories remained unchanged.[1]The 10 personality disorders are classified into 3 clusters. Cluster A includes paranoid, schizoid, and schizotypal personality disorders. Cluster B includes antisocial, borderline, histrionic, and narcissistic personality disorders. Cluster C includes avoidant, dependent, and obsessive-compulsive personality disorders. Personality disorders are currently described as pervasive, maladaptive, and chronic patterns of behavior, thinking, and feeling.[3][4]Patients with personality disorders often have distorted perceptions of reality and abnormal affective behavior, manifesting in maladaptive coping mechanisms and distress.[5]

The DSM-5-TRdefines a personality disorder as an enduring pattern of inner experience and behavior that deviates significantly from the norms and expectations of the surrounding culture. The behavioral pattern is pervasive, inflexible, and generally starts in adolescence and persists through adulthood, causing distress or impairments. Although there are 10 specific personality disorders listed in the DSM-5-TR, there is also a diagnosis for "general personality disorder" for clinical situations where a personality disorder is apparent but difficult to classify. This general diagnosis exists because personality is broad, case-specific, and unique, even among those with the same personality disorder diagnosis.[6]

The DSM-5-TR introduced an alternative diagnostic model for personality disorders in the Emerging Measures and Models section. The alternative diagnostic model for personality disorders in the DSM-5-TR is a hybrid dimensional-categorical model that defines personality disorders in terms of impairments in personality functioning and pathological personality traits.

Etiology

There are limited high-quality, evidence-based studies focused directly on the etiology of personality disorders, which are complex and multifactorial. Biological factors contribute to the development of personality in multiple ways. Temperament is a heritable and innate psychobiological characteristic that significantly contributes to personality development.[7][8]Temperament lays the framework for an individual's personality development. Personality is a pattern of behaviors that an individual uniquely adapts to address constantly changing internal and external stimuli.Temperament is further shaped through epigenetic mechanisms, namely, life experiences such as trauma and socioeconomic conditions. These are referred to as adaptive etiological factors in personality development.[9][10]Temperament traits includeharm avoidance,novelty seeking,reward dependence, andpersistence.

Harm avoidance involves a bias towards inhibiting behavior that would result in punishment or non-reward.[11]High harm avoidance results in fear of uncertainty, social inhibition, shy behavior, and avoidance of danger or the unknown. Low harm avoidance is pathological and evident in antisocial personality disorder, histrionic personality disorder, and borderline personality disorder.Novelty seekingdescribes an inherent desire to initiatenew activities likely to produce a reward signal.[12]Low novelty-seeking results in uninquiring, isolative, and stoical behaviors commonly seen in clusters A and C personality disorders; high novelty-seeking is evident in cluster B personality disorders.

Reward dependence describes the amount of desire to alter behaviors in response to social reward cues.[13]Low reward dependence results in isolative behaviors, with little need for social reward. Persistencedescribes the ability to maintain behaviors despite frustration, fatigue, and limited reinforcement. Low persistence is associated with indolence, inactivity, and ease of frustration.[13][14]Genetic factors have been attributed as significant contributors to the development of a personality disorder; this was supported by multiple studies that investigated twin, linkage, candidate gene association studies, genome-wide association studies, and polygenic analyses.[7]

Medical conditions are often associated with personality disorders or personality changes, specifically including those with pathology that may damage neurons. This includes but is not limited to head trauma, cerebrovascular diseases, cerebral tumors, epilepsy, Huntington disease, multiple sclerosis, endocrine disorders, heavy metal poisoning, neurosyphilis, and acquired immune deficiency syndrome (AIDS).[15]Psychoanalytic factors also contribute to the development of personality disorders. Psychoanalyst Wilhelm Reich described "character armor" as defense mechanisms that develop with personality types to relieve cognitive conflict from internal impulses and interpersonal anxiety. For example, individuals withcluster Atraits haveprojectiondefense mechanisms, and individuals withcluster Btraits tend to develop defense mechanisms of displacement, denial, projection, rationalization, and regression.[16]

Epidemiology

The World Health Organization has estimated the prevalence of having a personality disorder to be 6.1%.[17] The estimated prevalence of the 3 clusters (A, B, and C) are 3.6%, 1.5%, and 2.7%, respectively.[5] Within the psychiatric population, estimates for the prevalence of personality disorders can reach up to 30% and even higher in incarcerated populations.[18]Those with personality disorders are likely to be younger, unmarried, men oflower socioeconomic status, and lower education levels.[19]These findings are likely congruent with certain personality disorders known to be partially self-resolving or at least decreasing symptom severity with age.[20]

Pathophysiology

Limited high-quality, evidence-based investigations of neuroimaging and histopathological findings among personality disorders exist. Some studies proposethat there is a genetic link between schizophrenia and cluster A personality disorder, forming a spectrum of schizophrenia-like illnesses; however, the current clinical understanding of the relationship between cluster A personality disorders and schizophrenia is limited.[21]Some biologicalcorrelatesand physiological findings have been associated with cluster B personality disorders. Most of this research relates to antisocial personality disorder (and psychopathy) in studies of individuals in correctional settings. Underarousal of the autonomic nervous system has beenhypothesized as a pathophysiological mechanism forantisocial personality disorder. This hypothesis proposes that individuals withantisocial personality disorder (ASPD) require higher sensory input to produce normal brain functioning than normal subjects, causing affected individuals to seek higher sensory input to raise their arousal to more tolerable levels. The result may be a higher risk tolerance for situations with higher arousal.[22][23]Findings to support this suggestion are lower pulse rates, lower skin conductance, and increased amplitude on event-related potentials in patients with antisocial personality disorder.[24][25]Nearly 50% of individuals with ASPDdisorder exhibit various electroencephalogram (EEG) abnormalities, including more slow-wave activity.[23][26]

Researchers have also discovered abnormal central nervous system (CNS) functioning associated with ASPDon nervous system imaging. The prefrontal cortex, the superior temporal cortex, the amygdala-hippocampal complex, and the anterior cingulate cortex are likely involved.[27]In 1991, Raine published a study comparing 21 individuals with ASPDto 34 control subjects that showed reduced prefrontal gray matter in the subjects with ASPDcompared to control subjects on structural magnetic resonance imaging (MRI).[28]Grant reported a study comparing 18 men with ASPD and psychopathy to healthy controls that showed individuals with ASPD had a smaller orbitofrontal cortex volume onstructural MRI.[29]

Current neurobiological models ofborderline personality disorder link findings across neuroendocrinology, structural neuroimaging, and functional neuroimaging. Specific genes may be involved with disruptions in the hypothalamic-pituitary-adrenal axis consistent with stress-related changes and chronic elevation of cortisol, affecting emotional regulation and impulse control.[30]Neuroimaging studies haveidentified differences in the amygdala, hippocampus, and medial temporal lobes in patients with borderline personality disorder that may also be related to self-reported childhood trauma.[31][32]

Top-down control abnormalities are seenin borderline personality disorder, showingthat cortical activity to moderatethe amygdala (and other limbic areas) is impaired. Instead, behavior is driven from thebottom-up, meaning that amygdala activation is unmoderatedby higher-level cortical functions.[33]Studies also suggest that patients withborderline personality disorder may misattribute negative emotions (fear, anger, disgust) to neutral faces more than control patients despite having the perception of happy and upset faces equivalent to those groups.[34]On neuropsychological testing, patients withborderline personality disorder have impaired cognitive flexibility and increased impulsivity. No correlation was found betweenborderline personality disorder disordersymptom severity and cognitive function.[35][36]

The pathophysiology of cluster C personality disorders is poorly understood.Althoughobsessive-compulsive disorder andobsessive-compulsive personality disorderare separate conditions, they have intersecting traits. There is a hypothesis stating that in obsessive-compulsive personality disorder, there is a disruption in serotonergic neurotransmission similar to that seen in obsessive-compulsive disorder.[37]Neuroimaging has revealed anomalies in brain areas related to decision-making, emotional modulation, and habit formation. These studies emphasize the prefrontal cortex and the amygdala. However, the findings are preliminary, and more research is needed to understand the neurobiological aspects of obsessive-compulsive personality disorder and other cluster C personality disorders.[38]

History and Physical

The presentation of personality disorders is broad and variable. Further, eachpersonalityis unique due to the extensive spectrum of temperament variation and life experiences endured by individuals that shape their personality. Those with personality disorders may bear grudges, hold strong first impressions, have poor boundaries, or be distrustful of clinicians they encounter. Therefore, an individualized approach is needed in the evaluation of a patient with a suspected personality disorder to maintain therapeutic rapport, establish trust, and maintain safe and appropriate boundaries.

The chief complaint is likely to relate to psychiatric sequelae of an underlying personality disorder, such as depression, anxiety, impulsive behaviors, and substance abuse. Additional complaints may relate to psychosocial impairments resulting from the underlying personality disorder, including difficulties with interpersonal relationships, unsatisfactory academic history, and poor vocational performance.[39]Obtaining a thorough psychiatric history, medical history, social history, developmental history, and history of family dynamics is essential for diagnosis. The features ofpersonality disorderstypicallystart emerging in adolescence, andworsening pathological behaviors may increase through early adulthood beforethey become an inflexible pattern of thinking and action. Inquiring about the patient's capacity to make and maintain relationships with family, friends, and romantic partners can help clarify the personality disorder diagnosis.[40]

The mental status examination is crucial in assessing individuals for personality disorders. The specific elements and findings of the examination can vary dependingon each case. Assessment of patients should include the following:

  • Appearance:A general description of how the patient looks during the interview. Those with identity difficulties may have excessive or eccentric clothing or accessories. Poor grooming and hygiene levels can suggest problems with goal-driven behavior or poor persistence.

  • Attitude and behaviors: Ageneral description of how the patient acts during the interview, including various levels of cooperation, disinhibition, and regression. Attitude can describe interest level, candidness, shyness, fearfulness, orgrandiosity. The level of eye contact can be observed, which varies in personality disorders, particularly in those individuals with poor social interest. Document negative signs, such as avolition (lack of motivation), asociality (lack of desire for relationships), and alexithymia (lack of emotions).

  • Affect:Describe the quality and range of affect displayed by the individual. Some descriptions are angry, euthymic, dysphoric, irritable, euphoric, sad,or irritable.

  • Speech:Abnormalities include odd, vague, metaphorical, or stereotyped speech. Individuals with personality disorders may have more pauses, slower speech, and less pitch variability.

  • Thought content:Assess for auditory/visual/olfactory/tactile hallucinations, delusions, and thoughts of self-harm, suicidality, or harming others. Delusions can be grandiose, erotomanic, jealous, somatic, or persecutory/paranoid. Hallucinations are not characteristic of personality disorders and, if present, need further clinical investigation for diagnostic clarity. Transient paranoia is frequently associated with borderline personality disorder, but auditory hallucinations are not a primary symptom. Illusions can be present in certain personality disorders, particularly schizotypal personality disorder. Depersonalization and derealization can be present in personality disorders, particularly borderline personality disorder.

  • Thought process: This process describes how thoughts are formulated, organized, and processed.Document if the patient is clear and coherent or confused, tangential, loose, or disorganized.

  • Insight:Generally, individuals with personality disorders have a poor understanding of how their behaviors are related to their feelings, dysregulated emotions, and interpersonal difficulties. Insight can be fair or good in certain personality disorders despite persisting symptoms.

  • Judgment and impulse control:Poor judgment and poor impulse control are common in personality disorders andrange in severity depending on the individual.[41]

Evaluation

Diagnosis of a personality disorder is based on the longitudinal observation of an individual's behaviors to assess their functioning over time. The symptoms of a personality disorder may overlap with symptoms observed during acute psychiatric conditions such as mood disorders or substance use disorders. If possible, personality disorders should be diagnosed when there is not a concurrent acute psychiatric condition.[42]Personality disorders can also contribute to the exacerbation of another psychiatric illness and lead to hospitalization.[43]

Clinicians often develop a psychological reaction to individuals with personality disorders, which is known as "countertransference." This occurs due to the nature of the encounters, as individuals may be irritable, aggressive, suicidal, or engage in self-harm.[44]Clinicians must recognize signs of countertransference, which can negatively affect patient care.[45]When clinicians feel frustrated with patients who may have a personality disorder, it is helpful to use those feelings as an evaluation tool to guide diagnosis and treatment.[46][47]

Psychological testing can help diagnose personality disorders but is not generally needed for a clinical diagnosis when a sufficient history is available. The Minnesota Multiphasic Personality Inventory-2 and the Rorschach Perceptual Thinking Index may be used to verify the presence of a personality disorder.[48][49][50]To formally diagnose a personality disorder, individuals must meet the diagnostic criteria specified in theDSM-5-TR. The diagnosis requires a thorough evaluation that considers multiple sources of information, including personal history, collateral information, and a mental status examination. A comprehensive assessment allows clinicians to assess the individual's symptoms, functioning, and overall presentation to see if diagnostic criteria are met. Specific DSM-5-TR criteria exist for each specified personality disorder. There is also aDSM-5-TR diagnosis for general personality disorder.

DSM-5-TRCriteria forGeneral Personality Disorder

  • An enduring pattern of inner experience and behavior that deviates markedly from the expectations of the individual's culture. This pattern is manifested in 2 (or more) of the following areas:

    • Cognition (ie, ways of perceiving and interpreting self, other people, and events)

    • Affectivity (ie, the range, intensity, lability, and appropriateness of emotional response)

    • Interpersonal functioning

    • Impulse control

  • The enduring pattern is inflexible and pervasive across variouspersonal and social situations.

  • The enduring pattern leads to clinically significant distress or impairment in social, occupational, or other important areas of functioning.

  • The pattern is stable and of long duration, and its onset can be traced back at least to adolescence or early adulthood.

  • The enduring pattern is not better explained as a manifestation or consequence of another mental disorder.

  • The enduring pattern is not attributable to the physiological effects of a substance (eg, a drug of abuse, a medication) or another medical condition (eg, head trauma).

The DSM-5-TR introduced an alternative diagnostic model for personality disorders in the Emerging Measures and Models section. The alternative diagnostic model for personality disorders in the DSM-5-TR is a hybrid dimensional-categorical model that defines personality disorders in terms of impairments in personality functioning and pathological personality traits.

Alternative DSM-5Models for Personality Disorders: General Criteria for Personality Disorder

The essential features of a personality disorder include:

  • Moderate or greater impairment in personality (self/interpersonal) functioning

  • Having 1 or more pathological personality traits

  • The impairments in personality functioning and the individual's personality trait expression are relatively:

    • Inflexible and pervasive across a broad range of personal and social situations

    • Stable across time, with onsets that can be traced back to at least adolescence or early adulthood

    • Not better explained by another mental disorder

    • Not solely attributable to the physiological effects of a substance or another medical condition (eg, severe head trauma)

    • Not better understood as normal for an individual's developmental stage or sociocultural environment

Treatment / Management

Attention to the therapeutic alliance is crucial, no matter the treatment paradigm one adopts. Individuals with personality disorders may be provocative, aggressive, or irritable, and the clinician's thoughts and feelings (countertransference), as well as the treatment team's reactions, must be monitored closely. No standard treatment algorithm exists for most personality disorders.Frequently, patients with personality disorders present due to comorbid psychiatric conditions, which can benefit from appropriate treatment. In the absence of a comorbid psychiatric illness, only poor evidence exists that pharmacotherapy helps treat personality disorders, and there are no Food and Drug Administration-approved medications for specific personality disorders. With the exception of borderline personality disorder, there are no high-quality, evidenced-based psychotherapies for personality disorders.[51]

Often, individuals request treatment at the behest of a first-degree relative or friend. Generally, this occurs after maladaptive behaviors have created stress on another rather than internal distress from the individual with a personality disorder. Therefore, assessing the treatment goals in each specific case is essential. As personality disorders may not remit, the focus of treatment may be reducing interpersonal conflict and stabilizing psychosocial functioning.[52][53]Case management can assist patients with personality disorders in maintaining income, shelter, and connection to medical and mental health services and providing assistance with other basic needs.

Differential Diagnosis

Personality disorders are often comorbid with other psychiatric disorders, and many features of specific personality disorders resemble other psychiatric illnesses. The defining characteristics of personality disorders that appear before early adulthood are anenduring pattern of behavior that is inflexible and pervasive across a broad range of personal and social situations and does not occur exclusively during an episode of another mental disorder.[20] These characteristics can help distinguish personality disorders from episodic psychiatric illnesses, such as a major depressive episode, an anxiety disorder, or a manic episode.[54]Transient paranoia and psychosis are possible in certain personality disorders (primarily borderline personality disorder, schizotypal personality disorder, and paranoid personality disorder). Frank and persistent psychosis is not consistent with a personality disorder.[55]

After extreme stress, an individual's personality can change, and a diagnosis of posttraumatic stress should be considered. A personality disorder diagnosis should not be made when there are behaviors connected with substance intoxication or withdrawal or behaviors that are associated with sustaining substance use. Medical conditions are often associated with personality disorders or personality changes, specifically including those with pathology that may damage neurons. This includes but is not limited to head trauma, cerebrovascular diseases, cerebral tumors, epilepsy, Huntington disease, multiple sclerosis, endocrine disorders, heavy metal poisoning, neurosyphilis, and acquired immune deficiency syndrome (AIDS).[15]In these instances, a diagnosis of personality change due to another medical condition should be considered; an individual may have personality traits that do not reach the threshold for a personality disorder.

Pertinent Studies and Ongoing Trials

Experts in personality disorders have suggested switching to a dimensional model of personality rather than a cluster model. The dimensional models proposed generally describe temperament, utilization of defense mechanisms, and identifying pathological personality traits.[4]The DSM-5-TR introduced an alternative diagnostic model for personality disorders in the Emerging Measures and Models section; this includes a hybrid dimensional-categorical model that defines personality disorders in terms of impairments in personality functioning and pathological personality traits.

Prognosis

The prognosis of personality disorders varies depending on the specific personality disorder.Patients with borderline personality disorder have a fair prognosis, and studies demonstrate that borderline personality disorder psychopathology improves more than generally expected but that psychosocial functioning often remains impaired. Systematic meta-analysis with 5- to 15-year follow-up periods showed mean remission rates of 60%.[56]Despite high rates of remission and low rates of relapse, patients with borderline personality disorder have severe and persistent impairment in functional and social recovery. This is consistent with the theory that with stable support and avoidance of interpersonal stressors, patients with borderline personality disorder remit clinically.[56]

Individuals with antisocial personality disorder typically have severe pathology for life. However, in patients who achieve remission, the mean age is 35, and remission is predicted by less baseline symptomatology. Other factors that predict improved outcomes are older age at presentation, improved community ties, job stability, and marital attachment.[57][58][59]Other personality disorders have variable remission rates, and factors associated with remission (such as treatment and social stability) are poorly understood.

Complications

Substance use disorders are common among personality disorders but it is not clear which personality disorders pose the most risk for a particular substance use disorder.[60]Personality disorders have an increased likelihood of suicide and suicide attempts compared to those without personality disorders, and individuals with personality disorders should be screened for suicidal ideation regularly.[61]

Deterrence and Patient Education

Treating personality disorders depends ondeveloping and maintaining therapeutic rapport. Therapists should offer reassurance that the environment is safe and supportive. Patients are encouraged to articulatethe symptoms they wish to have addressed and communicate any psychosocial stressors that the treatment team can help alleviate. Rather than primarily focusing on changing the patient's worldview, clinicians should aim to understand and address the specific concerns and challenges that the individualis facing, especially when the patient is not in acute distress or crisis.[62]Further, patients are encouraged to utilize support networks through their remaining social relationships and expand on these as they develop comfort and confidence. Involving the patient's family is another way of monitoring for decompensation and providing education on how toprovide stable social factors for the patient.[63]Utilizing standardized assessments for quality of life may reveal ways to optimize the ability to function in significant areas of life for an individual with a personality disorder.

Enhancing Healthcare Team Outcomes

The diagnosis and treatment of personality disorders is a complicated topic but ultimately is an area of psychiatric research that requires further study.As diagnostic and treatment models shift away from a categorical cluster system and towards a dimensional model of personality, it is not clear what the implications will be forclinical practice. When a treatment team suspects an individual has a personality disorder, a comprehensive history with collateral information is recommended before diagnosing a personality disorder.[62]If the symptoms are first presenting in midlife, the individual should be evaluated for another medical condition or an unrecognized substance use disorder. Including the individual's perspective and determining the appropriate care goals are essential to prevent overmedicalization or iatrogenic harm to a patient who may not be suffering from any treatable symptoms. Collaboration with social workers, therapists, and family to optimize the social factors in a patient's life can offer stability to individuals with personality disorders. (Oxford Center for Evidence-Based Medicine, evidence level 5).

References

1.

Crocq MA. Milestones in the history of personality disorders. Dialogues Clin Neurosci. 2013 Jun;15(2):147-53. [PMC free article: PMC3811086] [PubMed: 24174889]

2.

Bassett D. Personality disorders: A Retrospective. Aust N Z J Psychiatry. 2017 Jul;51(7):658-659. [PubMed: 28633575]

3.

Wilson S, Stroud CB, Durbin CE. Interpersonal dysfunction in personality disorders: A meta-analytic review. Psychol Bull. 2017 Jul;143(7):677-734. [PMC free article: PMC5507693] [PubMed: 28447827]

4.

Trull TJ, Widiger TA. Dimensional models of personality: the five-factor model and the DSM-5. Dialogues Clin Neurosci. 2013 Jun;15(2):135-46. [PMC free article: PMC3811085] [PubMed: 24174888]

5.

Ma G, Fan H, Shen C, Wang W. Genetic and Neuroimaging Features of Personality Disorders: State of the Art. Neurosci Bull. 2016 Jun;32(3):286-306. [PMC free article: PMC5563771] [PubMed: 27037690]

6.

Oltmanns JR, Smith GT, Oltmanns TF, Widiger TA. General Factors of Psychopathology, Personality, and Personality Disorder: Across Domain Comparisons. Clin Psychol Sci. 2018 Jul;6(4):581-589. [PMC free article: PMC6132273] [PubMed: 30221082]

7.

Sanchez-Roige S, Gray JC, MacKillop J, Chen CH, Palmer AA. The genetics of human personality. Genes Brain Behav. 2018 Mar;17(3):e12439. [PMC free article: PMC7012279] [PubMed: 29152902]

8.

Réale D, Reader SM, Sol D, McDougall PT, Dingemanse NJ. Integrating animal temperament within ecology and evolution. Biol Rev Camb Philos Soc. 2007 May;82(2):291-318. [PubMed: 17437562]

9.

Svrakic DM, Cloninger RC. Epigenetic perspective on behavior development, personality, and personality disorders. Psychiatr Danub. 2010 Jun;22(2):153-66. [PubMed: 20562740]

10.

Gescher DM, Kahl KG, Hillemacher T, Frieling H, Kuhn J, Frodl T. Epigenetics in Personality Disorders: Today's Insights. Front Psychiatry. 2018;9:579. [PMC free article: PMC6252387] [PubMed: 30510522]

11.

Wan L, Zha R, Ren J, Li Y, Zhao Q, Zuo H, Zhang X. Brain morphology, harm avoidance, and the severity of excessive internet use. Hum Brain Mapp. 2022 Jul;43(10):3176-3183. [PMC free article: PMC9188967] [PubMed: 35332975]

12.

Gocłowska MA, Ritter SM, Elliot AJ, Baas M. Novelty seeking is linked to openness and extraversion, and can lead to greater creative performance. J Pers. 2019 Apr;87(2):252-266. [PubMed: 29604214]

13.

Frank GKW, Shott ME, Sternheim LC, Swindle S, Pryor TL. Persistence, Reward Dependence, and Sensitivity to Reward Are Associated With Unexpected Salience Response in Girls but Not in Adult Women: Implications for Psychiatric Vulnerabilities. Biol Psychiatry Cogn Neurosci Neuroimaging. 2022 Nov;7(11):1170-1182. [PubMed: 33872764]

14.

McGiboney GW, Carter C. Measuring persistence and personality characteristics of adolescents. Psychol Rep. 1993 Feb;72(1):128-30. [PubMed: 8451343]

15.

Leppla I, Fishman D, Kalra I, Oldham MA. Clinical Approach to Personality Change Due toAnother Medical Condition. J Acad Consult Liaison Psychiatry. 2021 Jan-Feb;62(1):14-21. [PubMed: 33190792]

16.

Shapiro D. Theoretical reflections on Wilhelm Reich's Character Analysis. Am J Psychother. 2002;56(3):338-46. [PubMed: 12400201]

17.

Tyrer P, Reed GM, Crawford MJ. Classification, assessment, prevalence, and effect of personality disorder. Lancet. 2015 Feb 21;385(9969):717-26. [PubMed: 25706217]

18.

Schnittker J, Larimore SH, Lee H. Neither mad nor bad? The classification of antisocial personality disorder among formerly incarcerated adults. Soc Sci Med. 2020 Nov;264:113288. [PMC free article: PMC8278498] [PubMed: 32858490]

19.

Zhang TT, Huang YQ, Liu ZR, Chen HG. Distribution and Risk Factors of Disability Attributed to Personality Disorders: A National Cross-sectional Survey in China. Chin Med J (Engl). 2016 Aug 05;129(15):1765-71. [PMC free article: PMC4976561] [PubMed: 27453222]

20.

Biskin RS. The Lifetime Course of Borderline Personality Disorder. Can J Psychiatry. 2015 Jul;60(7):303-8. [PMC free article: PMC4500179] [PubMed: 26175388]

21.

Laguerre A, Leboyer M, Schürhoff F. [The schizotypal personality disorder: historical origins and current status]. Encephale. 2008 Jan;34(1):17-22. [PubMed: 18514146]

22.

Raine A. Autonomic nervous system factors underlying disinhibited, antisocial, and violent behavior. Biosocial perspectives and treatment implications. Ann N Y Acad Sci. 1996 Sep 20;794:46-59. [PubMed: 8853591]

23.

Dolan M. Psychopathy--a neurobiological perspective. Br J Psychiatry. 1994 Aug;165(2):151-9. [PubMed: 7953028]

24.

Raine A, Venables PH, Williams M. Relationships between central and autonomic measures of arousal at age 15 years and criminality at age 24 years. Arch Gen Psychiatry. 1990 Nov;47(11):1003-7. [PubMed: 2241502]

25.

Scarpa A, Raine A. Psychophysiology of anger and violent behavior. Psychiatr Clin North Am. 1997 Jun;20(2):375-94. [PubMed: 9196920]

26.

Moffitt TE, Lynam D. The neuropsychology of conduct disorder and delinquency: implications for understanding antisocial behavior. Prog Exp Pers Psychopathol Res. 1994:233-62. [PubMed: 8044205]

27.

Dolan MC. What imaging tells us about violence in anti-social men. Crim Behav Ment Health. 2010 Jul;20(3):199-214. [PubMed: 20549783]

28.

Raine A, Lencz T, Bihrle S, LaCasse L, Colletti P. Reduced prefrontal gray matter volume and reduced autonomic activity in antisocial personality disorder. Arch Gen Psychiatry. 2000 Feb;57(2):119-27; discussion 128-9. [PubMed: 10665614]

29.

Grant BF, Hasin DS, Stinson FS, Dawson DA, Chou SP, Ruan WJ, Pickering RP. Prevalence, correlates, and disability of personality disorders in the United States: results from the national epidemiologic survey on alcohol and related conditions. J Clin Psychiatry. 2004 Jul;65(7):948-58. [PubMed: 15291684]

30.

Ruocco AC, Carcone D. A Neurobiological Model of Borderline Personality Disorder: Systematic and Integrative Review. Harv Rev Psychiatry. 2016 Sep-Oct;24(5):311-29. [PubMed: 27603741]

31.

Cattane N, Rossi R, Lanfredi M, Cattaneo A. Borderline personality disorder and childhood trauma: exploring the affected biological systems and mechanisms. BMC Psychiatry. 2017 Jun 15;17(1):221. [PMC free article: PMC5472954] [PubMed: 28619017]

32.

Peverill M, Rosen ML, Lurie LA, Sambrook KA, Sheridan MA, McLaughlin KA. Childhood trauma and brain structure in children and adolescents. Dev Cogn Neurosci. 2023 Feb;59:101180. [PMC free article: PMC9800267] [PubMed: 36563460]

33.

Kulacaoglu F, Kose S. Borderline Personality Disorder (BPD): In the Midst of Vulnerability, Chaos, and Awe. Brain Sci. 2018 Nov 18;8(11) [PMC free article: PMC6266914] [PubMed: 30453675]

34.

Law MK, Fleeson W, Arnold EM, Furr RM. Using Negative Emotions to Trace the Experience of Borderline Personality Pathology: Interconnected Relationships Revealed in an Experience Sampling Study. J Pers Disord. 2016 Feb;30(1):52-70. [PMC free article: PMC4547903] [PubMed: 25710731]

35.

Aslan IH, Grant JE, Chamberlain SR. Cognition in adults with borderline personality disorder. CNS Spectr. 2023 Dec;28(6):674-679. [PubMed: 36924168]

36.

Zimmerman M, Multach MD, Dalrymple K, Chelminski I. Clinically useful screen for borderline personality disorder in psychiatric out-patients. Br J Psychiatry. 2017 Feb;210(2):165-166. [PubMed: 27908898]

37.

Blom RM, Samuels JF, Riddle MA, Joseph Bienvenu O, Grados MA, Reti IM, Eaton WW, Liang KY, Nestadt G. Association between a serotonin transporter promoter polymorphism (5HTTLPR) and personality disorder traits in a community sample. J Psychiatr Res. 2011 Sep;45(9):1153-9. [PMC free article: PMC3128677] [PubMed: 21450307]

38.

Diedrich A, Voderholzer U. Obsessive-compulsive personality disorder: a current review. Curr Psychiatry Rep. 2015 Feb;17(2):2. [PubMed: 25617042]

39.

Ritzl A, Csukly G, Balázs K, Égerházi A. Facial emotion recognition deficits and alexithymia in borderline, narcissistic, and histrionic personality disorders. Psychiatry Res. 2018 Dec;270:154-159. [PubMed: 30248486]

40.

Bozzatello P, Garbarini C, Rocca P, Bellino S. Borderline Personality Disorder: Risk Factors and Early Detection. Diagnostics (Basel). 2021 Nov 18;11(11) [PMC free article: PMC8620075] [PubMed: 34829488]

41.

Storebø OJ, Stoffers-Winterling JM, Völlm BA, Kongerslev MT, Mattivi JT, Jørgensen MS, Faltinsen E, Todorovac A, Sales CP, Callesen HE, Lieb K, Simonsen E. Psychological therapies for people with borderline personality disorder. Cochrane Database Syst Rev. 2020 May 04;5(5):CD012955. [PMC free article: PMC7199382] [PubMed: 32368793]

42.

Clark LA. Assessment and diagnosis of personality disorder: perennial issues and an emerging reconceptualization. Annu Rev Psychol. 2007;58:227-57. [PubMed: 16903806]

43.

Campbell K, Clarke KA, Massey D, Lakeman R. Borderline Personality Disorder: To diagnose or not to diagnose? That is the question. Int J Ment Health Nurs. 2020 Oct;29(5):972-981. [PubMed: 32426937]

44.

Sansone RA, Sansone LA. Responses of mental health clinicians to patients with borderline personality disorder. Innov Clin Neurosci. 2013 May;10(5-6):39-43. [PMC free article: PMC3719460] [PubMed: 23882440]

45.

Parth K, Datz F, Seidman C, Löffler-Stastka H. Transference and countertransference: A review. Bull Menninger Clin. 2017 Spring;81(2):167-211. [PubMed: 28609147]

46.

Knaak S, Mantler E, Szeto A. Mental illness-related stigma in healthcare: Barriers to access and care and evidence-based solutions. Healthc Manage Forum. 2017 Mar;30(2):111-116. [PMC free article: PMC5347358] [PubMed: 28929889]

47.

Bodner E, Cohen-Fridel S, Mashiah M, Segal M, Grinshpoon A, Fischel T, Iancu I. The attitudes of psychiatric hospital staff toward hospitalization and treatment of patients with borderline personality disorder. BMC Psychiatry. 2015 Jan 22;15:2. [PMC free article: PMC4307152] [PubMed: 25609479]

48.

Widiger TA, Hines A, Crego C. Evidence-Based Assessment of Personality Disorder. Assessment. 2024 Jan;31(1):191-198. [PubMed: 37231676]

49.

Dao TK, Prevatt F, Horne HL. Differentiating psychotic patients from nonpsychotic patients with the MMPI-2 and Rorschach. J Pers Assess. 2008 Jan;90(1):93-101. [PubMed: 18444100]

50.

Sellbom M, Ben-Porath YS, Lilienfeld SO, Patrick CJ, Graham JR. Assessing psychopathic personality traits with the MMPI-2. J Pers Assess. 2005 Dec;85(3):334-43. [PubMed: 16318573]

51.

May JM, Richardi TM, Barth KS. Dialectical behavior therapy as treatment for borderline personality disorder. Ment Health Clin. 2016 Mar;6(2):62-67. [PMC free article: PMC6007584] [PubMed: 29955449]

52.

Weinberg I, Ronningstam E. Dos and Don'ts in Treatments of Patients With Narcissistic Personality Disorder. J Pers Disord. 2020 Mar;34(Suppl):122-142. [PubMed: 32186986]

53.

Bateman A, O'Connell J, Lorenzini N, Gardner T, Fonagy P. A randomised controlled trial of mentalization-based treatment versus structured clinical management for patients with comorbid borderline personality disorder and antisocial personality disorder. BMC Psychiatry. 2016 Aug 30;16(1):304. [PMC free article: PMC5006360] [PubMed: 27577562]

54.

Sanches M. The Limits between Bipolar Disorder and Borderline Personality Disorder: A Review of the Evidence. Diseases. 2019 Jul 05;7(3) [PMC free article: PMC6787615] [PubMed: 31284435]

55.

Schultze-Lutter F, Nenadic I, Grant P. Psychosis and Schizophrenia-Spectrum Personality Disorders Require Early Detection on Different Symptom Dimensions. Front Psychiatry. 2019;10:476. [PMC free article: PMC6637034] [PubMed: 31354543]

56.

Winsper C. Borderline personality disorder: course and outcomes across the lifespan. Curr Opin Psychol. 2021 Feb;37:94-97. [PubMed: 33091693]

57.

Black DW. The Natural History of Antisocial Personality Disorder. Can J Psychiatry. 2015 Jul;60(7):309-14. [PMC free article: PMC4500180] [PubMed: 26175389]

58.

Black DW, Monahan P, Baumgard CH, Bell SE. Predictors of long-term outcome in 45 men with antisocial personality disorder. Ann Clin Psychiatry. 1997 Dec;9(4):211-7. [PubMed: 9511944]

59.

Burt SA, Donnellan MB, Humbad MN, Hicks BM, McGue M, Iacono WG. Does marriage inhibit antisocial behavior?: An examination of selection vs causation via a longitudinal twin design. Arch Gen Psychiatry. 2010 Dec;67(12):1309-15. [PMC free article: PMC3057675] [PubMed: 21135331]

60.

Parmar A, Kaloiya G. Comorbidity of Personality Disorder among Substance Use Disorder Patients: A Narrative Review. Indian J Psychol Med. 2018 Nov-Dec;40(6):517-527. [PMC free article: PMC6241194] [PubMed: 30533947]

61.

Boot K, Wiebenga JXM, Eikelenboom M, van Oppen P, Thomaes K, van Marle HJF, Heering HD. Associations between personality traits and suicidal ideation and suicide attempts in patients with personality disorders. Compr Psychiatry. 2022 Jan;112:152284. [PubMed: 34763292]

62.

Lampe L, Malhi GS. Avoidant personality disorder: current insights. Psychol Res Behav Manag. 2018;11:55-66. [PMC free article: PMC5848673] [PubMed: 29563846]

63.

Kotlicka-Antczak M, Karbownik MS, Pawełczyk A, Żurner N, Pawełczyk T, Strzelecki D, Urban-Kowalczyk M. A developmentally-stable pattern of premorbid schizoid-schizotypal features predicts psychotic transition from the clinical high-risk for psychosis state. Compr Psychiatry. 2019 Apr;90:95-101. [PubMed: 30831438]

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