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===Other Diagnostic Studies===
===Other Diagnostic Studies===
[[Electroencephalographic]] (EEG) changes are observed in PD, however, they are not diagnostic. The presence of sharp and spike waves may be a common finding in BPD.


==Treatment==
==Treatment==

Revision as of 18:23, 16 July 2021

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Personality disorder Microchapters

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Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Personality disorder from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Personality Change Due to Another Medical Condition

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

MRI

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Ayesha Anwar, M.B.B.S[2]

Overview

Personality disorders (PD) are described as unique, long-term pervasive patterns of expressing and manifesting emotions, thoughts, and behaviors in an inflexible and maladaptive manner leading to significant functional impairment in one's life. Personality traits, in contrast, are specific patterns of thinking, perceiving, and responding to different situations in an adaptive and tenaciously stable way throughout life. The personality traits formulate an essential aspect in one's life in facing and dealing with contrasting situations as maladaptive personality can result in clinical distress and psychosocial impairment. In order to differentiate normal responses from abnormal or pathological, the criterion employed requires behaviors displayed by a majority in the population as normal and pathological if they are rare or there is the absence of a sense of contentment and adaptability to the social environment or marked deviation from cultural expectations. Hence, these are relative terms, and therefore, the Diagnostic and Statistical Manual of Mental Disorders (DSM) has established a set criterion for diagnosing personality disorders. This is based on the presence of impaired personality functioning and pathological traits. The pathophysiology of PD remains unclear to date. There are countless complex psychodynamic theories explaining the development of the disorder. Both genetic and environmental factors interplay in the causation of PD. A decrease in monoamine oxidase (MAO), and serotonin levels are seen with multiple PD. Although mostly recognized and diagnosed in adults, PD is present and develops in youth and adolescence. About 1 in 10 adolescents meets the criteria for PD. There are ten personality traits classified into 3 clusters; A, B, and C, based on similar characteristics. A clinical criterion as set by DSM-V is used for the diagnosis after the exclusion of other similar conditions (mental health disorder, substance use disorder, structural central nervous system (CNS) disorder). For most personality disorders, an age greater than 18 years is required for the diagnosis. This disorder is retained throughout an individual's life; however, certain types become less intense with age. The presence of PD is associated with increased mortality. The increased mortality is associated with unnatural causes like suicide, accidents, homicide, substance abuse, and depression. Natural death chances may also be enhanced in PD due to negative perspectives and emotions regarding health problems in life and the correlation of impaired mental health with physical health. Alcoholism and substance abuse contribute as precipitating factors and complications in PD. Psychotherapy remains the mainstay of treatment in both management and preventing complications. Medications are used as adjuncts. Cognitive-Behavioral therapy, impulse control, interpersonal psychotherapy, self-help groups, and family therapy are required. Medical therapy is required to balance and restore the neurotransmitter abnormalities associated with PD. Among them, Selective serotonin reuptake inhibitors(SSRIs) and newer antidepressants remain the hallmark. Antipsychotics and mood stabilizers also help. Despite individual and supportive psychotherapy, treatment of PD remains challenging and difficult.

Historical Perspective

Personality defects were started to be recognized in the 18th century. Previously, all the diseases were a result of abnormalities with four bodily fluids; blood, phlegm, yellow bile, and black bile. The changes in them were also considered responsible for variations in mood. However, by the 18th century, Phillippe Pinel described a group of people having impulsive, irrational ways and behaviors while maintaining understanding, perception, judgment, and memory of the actions. This was the birth of recognition of personality disorders. In the 18th century, the term 'phrenology' was used to describe personality characteristics. It was believed that the origin of personality traits is from various facets in the cranium. Despite the discontinuation of the term, it remains significant as it laid the basis for the origin of PDs from the cerebral cortex. In the 19th century and early 20th century, different European psychologists started identifying and describing different personality traits and disorders. The term personality is derived from Greek word, 'persona,' the mask worn in theatres in ancient times to denote a character or social role. It is now used to define that aspect of the person which is discerned by other individuals. In the 1920s and 1930s, Sigmund Freud, known as the father of psychology and his colleagues, worked on the psychoanalytic classification and etiology of personality. They related personality traits with childhood characters. He presented the structural theory that unconscious mental conflicts influence the development of character and behavior [1]. This comprises three components of the brain; the id (primitive urges at birth), ego (mediator that maintains a balance between id and reality), and superego (conscience and moral values). They develop at different stages in life, and the interplay among them is responsible for shaping the personality of a person. Any fixation at any stage is responsible for the improper balance of id and ego and leads to interference in the appropriate and timely development of the superego. A person is born with the id and develops ego and superego at last. This laid down the foundation for further theories and explanations of PDs; however, it lacks the interaction and influences of social, cultural, environmental, and genetic factors in posing the personality in an individual. In the late 1900s, statistics was utilized to group together different definitions of personality structures. It was pioneered by Bernard Cattell. This employs a different number of dimensions to delineate personality systems. These dimensional models lead to DSM characterization of personality disorders according to DSM classifications. DSM II was established in 1986 and listed 10 PDs. It differs from DSM I due to the recognition stage in life being adolescence, while the former states that these disorders exist lifelong. DSM II was based on concepts of psychoanalysis and neuroses, while DSM III described PDs scientifically and clinically. DSM IV was established in 1994 with an updated version, DSM IV-TR, and uses a multiaxial approach to describe psychiatric illnesses with axis II reserved for personality disorder. This multiaxial system was abolished in DSM 5 and categorized the various disorders with related disorders [2]. It classifies PDs into three clusters, with each containing 3-4 disorders.

Classification

There are two approaches used to classify personality disorders; categorical and dimensional. Categorical classification is based on distinct operational criteria depending on behavioral characteristics. DSM-5 and ICD-10 both uses this approach. As compared to this, dimensional classification is based on the personality traits and using a quantitative distinction. It places normality at one end and disorder at other.

Pathophysiology

The exact pathogenesis of personality disorder is not fully understood. Personality disorders are related to multifactorial causes. Throughout time, a multitude of theories has been developed to explain the origin of these disorders. However still, the pathophysiology of PDs remains enigmatic. The five-factor model of personality was developed in the 1980s and 1990s, which demonstrated that it comprises five distinct traits. PDs are primarily the result of positive correlation with Neuroticism and negative association with Agreeableness. Extraversion is associated in both ways . It is a well-known fact that personality develops during childhood and interpersonal experiences and social interactions play a significant role in the development of PDs. Parental maltreatment, stress, and traumatic life events influence the personality adversely. In addition, genetic and prenatal factors also constitute a major role. Genetic factors with mutations in genes involving dopamine and serotonin pathways such as DRD2, COMT, DTNBP1, DAAO, 5-HTTLPR, MAOA, DRD3,TPH1 and TPH2 Perinatal injuries like trauma, infections like encephalitis, and hemorrhage may also be contributing factors. Genetic factors interact with environmental stresses to result in PDs. Various parental behavior like excessive attachment, parental insensitivity or emotional neglect, physical and sexual abuse, and substance use disorders causes an essential impact on PDs development. Social bullying, racial discrimination, frequent dislocations during childhood, and lack of peer support are other risk factors.

==Causes==Causative factors associated with PDs include:

  1. Genetic factors with mutations in genes involving dopamine and serotonin pathways such as DRD2, COMT, DTNBP1, DAAO, 5-HTTLPR, MAOA, DRD3,TPH1 and TPH2.
  2. Environmental factors like stresses, parental treatment, sexual abuse and substance use.

Differentiating Personality disorder from Other Diseases

Epidemiology and Demographics

Worldwide pooled prevalence of personality disorder as found by meta-analysis of studies conducted from 21 countries is 7.8%. Global rates of cluster-A PD is 3.8%, cluster-B is 2.8% and cluster-C PD is 5% [3]. In United States (US), it is around 10%, with major disease burden contributed by obsessive-compulsive PD followed by narcissist and borderline PD. In the rest of countries, it varies [4]. OCD is twice common in females than males and 75% of individuals diagnosed with BPD are females. No sex predilection is found with rest. Narcissist PD is found in 20% of military personals, 17% first-year medical students and 6% forensic population.

Risk Factors

The exact cause of personality disorder remains unknown. However, it usually results from the interplay of genetic and environmental factors. The risk of development of personality disorder is increased by the presence of certain factors such as perinatal injuries, family history, history of substance abuse, childhood abuse and other psychosocial factors.

Screening

Natural History, Complications, and Prognosis

Personality disorders usually begin to develop in early adolescence and are diagnosed in early adulthood. The symptoms are usually apparent for a long time, indicating the long-term course of the disorder in life. Moreover, it also affects functioning in several aspects that can cause personal impairment and social distress. Stigmatization exists after the diagnosis is established and prevents individuals from seeking treatment at an earlier stage. However, with appropriate psychotherapy and keeping symptoms under control with medications, disease stability is achieved and even complete remission. A follow-along study performed by Skodol et al. demonstrated that remission was seen in the case of avoidant and schizotypal PD with a greater number of positive experiences and building interpersonal skills at a young age. Another ten years follow-up study to observe remission in BPD was done by Zanarini et al., which revealed that 80% of individuals achieved remission and their 16 years follow-up showed sustained symptomatic remission [5] [6]. The complications can occur at any stage and can add to a worsening prognosis. Among them, suicidality is of foremost significance. Others include injuries from fights and accidents, sexually acquired infections from presumptuous sex, and substance use disorder. It also adds to the morbidity by causing personal functional impairment and affecting family life. The mortality in PD is more than in the general population. A famous study spanning 24 years was performed on patients with PDs, and it was found that 5.9% of patients with BPD died by suicide vs. 1.4% of the comparison group and 14% vs. 5.5% with other non-suicide causes. In addition, those patients who did not achieve recovery were at higher risk of early death [7]. Thus, PDs follow a waxing and waning course throughout life with periods marked by flares and remission. The life expectancy in such individuals is influenced by psychotherapy initiation, treatment compliance, co-morbid conditions, and social support. In most cases, it is lesser than average in the normal individual.

Diagnosis

Diagnostic Study of Choice

The diagnosis of personality disorder is intricate as most patients present with symptoms related to depression and anxiety, and many times, two or more personality disorders co-exist. Also, an overlap in certain personality characteristics among different personality disorders. Therefore, the diagnosis of a personality disorder requires a specific criterion after a complete evaluation of cognitive, behavioral, interpersonal, and social features in an individual. DSM-5 and ICD-10 criteria are usually employed for this purpose.

History and Symptoms

History constitutes the first step in assessing for the personality disorder in any individual. The hallmark of personality disorders is an enduring and prolonged duration of presence of symptoms. An age of 18 years for a patient is essential in the diagnosis. The history varies with each type of personality disorder. Generally, a history of mood dysregulation and poor social interaction is suggestive of it.

Physical Examination

There are no specific physical signs associated with personality disorders. The physical exam is essential to rule out organic disorders and substance use disorders. Depression and anxiety need to be ruled out by conducting their assessment tools. Patients with borderline personality disorders have an increased risk of suicide, and they may have self-inflicted wounds on the body or signs of attempted suicide attempts. A complete mental status examination needs to be conducted. The first is to examine appearance and behavior. Borderline personality disorder patients may exhibit defensive behavior. Those with a paranoid personality disorder will fail to maintain eye contact. The second is mood and affect; borderline personality disorder may reveal fleeting mood and emotional states with different questions or scenarios. This is also vital to assess suicide risk in the patient. Antisocial personality disorders may be homicidal and display a hostile attitude. Cognitive functions like attention, memory, orientation, language, and intelligence are normal. Mini-mental state examination (MMSE) can be conducted for this. Histrionic PD may manifest a ‘la belle indifference,’ meaning showing an apparent lack of concern regarding their own symptoms. Perception is normal though. Moreover, the thought process is usually unremarkable. It is imperative in paranoid personality disorder to ascertain that no thoughts of harm to others are present. However, insight and judgment may be affected depending on different scenarios in patients with variable personality disorders.

Laboratory Findings

There are no diagnostic laboratory findings associated with personality disorders. Most laboratory tests are carried out to rule out other medical conditions which may present with personality changes. These tests include measurement of vitamin D, vitamin B12, ferritin, glucose and cortisol. PDs have concomitant substance abuse disorder and impulse control disorders. Hence, toxicology screen and sexually transmitted disease screening is crucial.

Electrocardiogram

X-ray

Echocardiography and Ultrasound

CT scan

There are no CT scan findings associated with personality disorder.

MRI

The MRI changes observed in borderline PD are found in hypothalamus and limbic system. The volumetric changes in gray matter in various regions of brain are associated with rest of PDs.

Other Imaging Findings

Positron emission tomography (PET) is another modality to assess the brain metabolism in different regions in different PDs. PET scan in BPD reveals hypometabolism of glucose in prefrontal cortex and limbic system

Other Diagnostic Studies

Electroencephalographic (EEG) changes are observed in PD, however, they are not diagnostic. The presence of sharp and spike waves may be a common finding in BPD.

Treatment

Medical Therapy

Interventions

Surgery

Primary Prevention

Secondary Prevention

References

  1. "The History of Personality Disorders | HealthyPlace".
  2. Crocq MA (2013). "Milestones in the history of personality disorders". Dialogues Clin Neurosci. 15 (2): 147–53. PMC 3811086. PMID 24174889.
  3. Winsper C, Bilgin A, Thompson A, Marwaha S, Chanen AM, Singh SP; et al. (2020). "The prevalence of personality disorders in the community: a global systematic review and meta-analysis". Br J Psychiatry. 216 (2): 69–78. doi:10.1192/bjp.2019.166. PMID 31298170.
  4. Sansone RA, Sansone LA (2011). "Personality disorders: a nation-based perspective on prevalence". Innov Clin Neurosci. 8 (4): 13–8. PMC 3105841. PMID 21637629.
  5. Zanarini MC, Frankenburg FR, Hennen J, Reich DB, Silk KR (2006). "Prediction of the 10-year course of borderline personality disorder". Am J Psychiatry. 163 (5): 827–32. doi:10.1176/ajp.2006.163.5.827. PMID 16648323.
  6. Zanarini MC, Frankenburg FR, Reich DB, Fitzmaurice G (2012). "Attainment and stability of sustained symptomatic remission and recovery among patients with borderline personality disorder and axis II comparison subjects: a 16-year prospective follow-up study". Am J Psychiatry. 169 (5): 476–83. doi:10.1176/appi.ajp.2011.11101550. PMC 3509999. PMID 22737693.
  7. Temes CM, Frankenburg FR, Fitzmaurice GM, Zanarini MC (2019). "Deaths by Suicide and Other Causes Among Patients With Borderline Personality Disorder and Personality-Disordered Comparison Subjects Over 24 Years of Prospective Follow-Up". J Clin Psychiatry. 80 (1). doi:10.4088/JCP.18m12436. PMID 30688417) Check |pmid= value (help).

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