SYMPOSIA
SYMPOSIA
SYMPOSIA
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Bulletin of Clinical Psychopharmacology, Vol: 21, Supplement: 2, 2011 - www.psikofarmakoloji.org<br />
Abstracts of the Invited Speakers<br />
Individuals with CT have both an overall increased risk for depression and a substantially increased sensitivity to the depressogenic<br />
effects of stressful life events. The relation between CT and stressful life events is dose dependent and correlated with the intensity of the<br />
neuroticism. It has been shown that the severity of CT predicts an early age of onset and the number of life time depressive episodes,<br />
and that it is associated with more comorbidity. Increased rates of emotional CT, depressive symptoms and anxiety have been reported<br />
in treatment resistant group of patients.<br />
Childhood adverse life events are associated with various neuroendocrine and neuroanotomical changes. There is a 6 times larger ACTH<br />
response to stress in depressive female patients who reported CT. These patients also have an increased cortisol response and heart<br />
rate response to psychosocial stress. Women, who have reported CT but were not depressed, have exhibited normal cortisol responses,<br />
despite having increased an ACTH response. This can be interpreted as resilience against depression, an adrenal adaptation to central<br />
sensitization. It has been reported that decreased hippocampal volume (18%) in depression is related to CT and that the hippocampal<br />
volumes of depresssive patiens who did not report CT were equal to those of the control group. Repeated bursts of CRF in response to<br />
stress during development and increased cortisol reactivity over the course of time may contribute to smaller hippocampi after childhood<br />
trauma exposure, leading to further sensitization of the stress responses. These results would suggest that there are biologically distinct<br />
subtypes of depression as a function of childhood trauma.<br />
The effect of CT on predisposition to illness is associated with genotype. The s/s allele of the serotonin transporter gene, the gene<br />
polymorphism of BDNF and the CRF-1 gene have been shown to be related to vulnerability to trauma effects.<br />
CT is associated to decreased response to pharmacological treatment. Among chronically depressed patients with no history of early<br />
trauma, combination treatment was most effective in attaining remission compared to pharmacotherapy and psychotherapy. In contrast,<br />
in chronically depressed patients with early-life trauma, remission rates were significantly higher for psychotherapy alone versus<br />
pharmacotherapy. Combination treatment did not have any further advantage over psychotherapy alone. Improved effects of cognitive<br />
and behavioral therapies, group therapies and EMDR have been reported in various studies. Questioning about CT in MD patients seems<br />
to be important for treatment planning, assessment of risks and prophylactic interventions.<br />
Key words: Childhood trauma, mood disorders<br />
Bulletin of Clinical Psychopharmacology 2011;21(Suppl. 2):S78-9<br />
Trauma and psychotic disorders<br />
Selma Bozkurt Zincir<br />
Erenkoy Mental Health and Diseases Training and Research Hospital, Istanbul, Turkey<br />
E-mail: sbozkurtzincir@yahoo.com<br />
In recent years, there has been a growing awareness of the importance of abuse or trauma in shaping the course of people’s lives. There<br />
is growing literature to indicate that trauma is also linked with more severe psychiatric disturbances, including symptoms indicative of<br />
psychosis in general and schizophrenia in particular. Several lines of evidence suggest an association between trauma and psychosis with<br />
a dose-response effect. First, studies have demonstrated a high incidence of trauma in the lifetimes of patients with psychosis. Abused<br />
patients are particularly likely to experience positive symptoms, such as paranoid ideation, thought insertion, visual hallucinations, ideas<br />
of reading someone else’s mind, ideas of reference, and hearing voices making comments. Secondly, it has been suggested that of all<br />
diagnostic categories, psychosis displays the strongest association with child abuse. Thirdly, according to some researchers childhood<br />
sexual abuse is the most powerful predictor of later psychiatric symptoms and disorders after controlling for significant demographic<br />
variables.<br />
It has been suggested that the experience of abuse may create a biological or psychological vulnerability for the development of<br />
psychotic symptoms, including sub-clinical psychotic experiences such as low-grade delusional ideation, suicidal thinking and isolated<br />
auditory hallucinations. Exposure to psychological trauma worsens the prognosis of expression of psychosis, in terms of greater likelihood<br />
of transition to a more severe psychotic state. According to recent cognitive models of psychosis early adverse experiences such as<br />
social marginalization, childhood loss or severe childhood trauma may create an enduring cognitive vulnerability characterized by less<br />
subjective control over these experiences, negative schematic models of the self and a world that facilitates external attributions. This<br />
tendency to externally attribute events may lie beneath paranoid ideation.<br />
Current ideas about biological consequences of early adversities lend even more credibility to the notion of an enduring psychological<br />
vulnerability. It has been suggested that adverse life events or significant losses might be able to mould the neurodevelopmental<br />
abnormalities that underlie sensitivity to stressors, if they occur early enough or are sufficiently severe. Thus abnormal neurodevelopmental<br />
processes may originate from traumatic events in childhood. Specifically, when exposure to stressors persists and heightened stress-<br />
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