User:Irfan Dotani
Irfan Dotani
Irfan Dotani, Student
Contact: 515-509-6250
Email: irfandotani123@gmail.com
Current Position
Student Research Fellow, PERFUSE Study Group
Professional Background
Irfan Dotani is a student research fellow of cardiovascular medicine at the PERFUSE Study Group at Beth Israel Deaconess Medical Center. He is a sophomore at Bowdoin College and is 18 years of age. He has a deep interest in the medical field and hopes to one day pursue his goals and dreams of contributing to the medical field. Irfan is a contributor to multiple chapters, including St. Louis encephalitis, Osteoarthritis, Borderline Personality Disorder, etc.
Education
2021'-Expected graduate date from Bowdoin College.
Causes
Researchers commonly believe that BPD results from a combination of a traumatic childhood, a vulnerable temperament, and stressful maturational events during adolescence or adulthood.[1] Otto Kernberg formulated the theory of Borderline Personality based on a premise of failure to develop in childhood. There are, according to Kernberg, three developmental tasks an individual must accomplish; when one fails to accomplish a certain developmental task, this often corresponds with an increased risk of developing certain psychopathologies. Failing the first developmental task,psychic clarification of self and other, may result in an increased risk to develop varieties of psychosis. Not accomplishing the second task, overcoming splitting, may result in an increased risk to develop a borderline personality. [2]
Causes of Borderline Personality Disorder
Etiology | Description |
---|---|
Childhood abuse, Trauma, or Negelct |
|
Genetics |
An overview of the existing literature suggested that traits related to BPD are influenced by genes, and since personality is generally quite heritable then BPD should also be, but studies have had methodological problems and the links are not yet clear.[27] A major twin study found that if one identical twin met criteria for BPD, the other also met criteria in around a third (35%) of cases.[28] Twin, sibling and other family studies indicate a partially heritable basis for impulsive aggression, but studies of serotonin-related genes to date have suggested only modest contributions to behavior.[22] |
Neurofunction |
Neurotransmitters implicated in BPD include serotonin, norepinephrine and acetylcholine (related to various emotions and moods); GABA, the brain's major inhibitory neurotransmitter (which can stabilize mood change); and glutamate, an excitatory neurotransmitter. Enhanced amygdala activation in BPD has been identified as reflecting the intense and slowly subsiding emotions commonly observed in BPD in response to even low-level stressors. The activation of both the amygdala and prefrontal cortical areas can reflect attempts to control intensive emotions during the recall of unresolved life events.[29] Impulsivity or aggression, as sometimes seen in BPD, has been linked to alterations in serotonin function and specific brain regions in the cingulate and the medial and orbital prefrontal cortex.[22] |
Other Developmental Factors |
Some studies suggest that BPD may not necessarily be a trauma-spectrum disorder and that it is biologically distinct from the post traumatic stress disorder that could be a precursor. The personality symptom clusters seem to be related to specific abuses, but they may be related to more persistent aspects of interpersonal and family environments in childhood.[22] There is evidence for the central role of the family in the development of BPD, including interactions that are negative and critical rather than supportive and empathic, with parental and family behaviors transacting with the child's own behaviors and emotional vulnerabilities.[23] Some findings suggest that BPD may lie on a bipolar spectrum, with a number of points of phenomenological and biological overlap between the affective lability criterion of borderline personality disorder and the extremely rapid cycling bipolar disorders.[24][25] Some findings suggest that the DSM-IV BPD diagnosis mixes up two sets of unrelated items—an affective instability dimension related to Bipolar-II, and an impulsivity dimension not related to Bipolar-II.[26] |
- ↑ Zanarini, M.C.; F.R. Frankenburg (1997). "Pathways to the development of borderline personality disorder". Journal of Personality Disorder. 11 (1): 93-104. Retrieved on 2007-09-21.
- ↑ Kernberg, O. (2000). Borderline Conditions and Pathological Narcissism. New York: Aronson. ISBN 0876687621.