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1.
Biol Psychiatry ; 55(10): 1001-6, 2004 May 15.
Article in English | MEDLINE | ID: mdl-15121484

ABSTRACT

BACKGROUND: Previous imaging studies demonstrated that schizophrenia is associated with increased amphetamine-induced dopamine (DA) release in the striatum, most pronounced during episodes of illness exacerbation. Schizotypal personality disorder (SPD) is a schizophrenia spectrum disorder, genetically related to schizophrenia. The goal of this study was to investigate striatal DA function in patients with SPD. METHODS: In our study, 13 SPD patients and 13 matched healthy control subjects underwent single photon emission computed tomography (SPECT) scan during bolus plus constant infusion of the D2/3 radiotracer [123I]iodobenzamide (IBZM). Striatal specific to nonspecific equilibrium partition coefficient (V(3)") was measured at baseline and following amphetamine administration (.3 mg/kg). RESULTS: No significant differences were observed in baseline V(3)" between groups. Amphetamine induced a larger decrease in [123I]IBZM V(3)" in SPD patients (-12 +/- 5%) compared with control subjects (-7 +/- 5%, p =.03). CONCLUSIONS: The reduction in [123I]IBZM V(3)" induced by amphetamine in SPD was similar to that observed in remitted schizophrenia patients (-10 +/- 9%, n = 17), but significantly lower than that observed during illness exacerbation (-24 +/- 13%, n = 17). This suggests that DA dysregulation in schizophrenia spectrum disorders might have a trait component, present in remitted patients with schizophrenia and in SPD, and a state component, associated with psychotic exacerbations but not SPD.


Subject(s)
Amphetamine/pharmacology , Benzamides , Corpus Striatum/metabolism , Dopamine/metabolism , Pyrrolidines , Schizoid Personality Disorder/metabolism , Adult , Amphetamine/blood , Analysis of Variance , Case-Control Studies , Central Nervous System Stimulants/pharmacology , Dopamine Antagonists , Female , Humans , Iodine Radioisotopes , Male , Middle Aged , Psychiatric Status Rating Scales , Receptors, Dopamine D2/metabolism , Schizoid Personality Disorder/diagnostic imaging , Tomography, Emission-Computed, Single-Photon
2.
Psychopharmacology (Berl) ; 176(3-4): 451-8, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15160265

ABSTRACT

RATIONALE: Impulsive aggressive personality disordered patients have been shown to have decreased relative glucose metabolism in orbito-frontal cortex and anterior cingulate gyrus compared with normal subjects. In addition, patients with impulsive aggression have an attenuation of symptoms with selective serotonin reuptake inhibitor (SSRI) treatment. OBJECTIVES: The goals of the present study were to attempt to replicate the finding of improvement in impulsive aggression in borderline personality disorder with SSRIs and to investigate the specific cortical areas modified by medication, which might underlie the observed clinical improvement using (18)FDG-PET. METHODS: Ten impulsive aggressive patients with borderline personality disorder were imaged with (18)F-deoxyglucose positron emission tomography at baseline and after receiving fluoxetine at 20 mg/day for 12 weeks. Anatomical MRIs were coregistered to PET and relative metabolic rates were obtained in 39 Brodmann areas. RESULTS: Brodmann areas 11 and 12 in the orbito-frontal cortex showed significant increases in relative metabolic rate. Significant clinical improvement was also observed as assessed by the Overt Aggression Scale-Modified. CONCLUSIONS: These changes are consistent with a normalizing effect of fluoxetine on prefrontal cortex metabolism in impulsive aggressive disorder.


Subject(s)
Aggression/physiology , Antidepressive Agents, Second-Generation/therapeutic use , Fluoxetine/therapeutic use , Impulsive Behavior/metabolism , Prefrontal Cortex/metabolism , Adult , Aggression/drug effects , Aggression/psychology , Antidepressive Agents, Second-Generation/adverse effects , Double-Blind Method , Female , Fluorodeoxyglucose F18 , Fluoxetine/adverse effects , Humans , Image Processing, Computer-Assisted , Impulsive Behavior/diagnostic imaging , Impulsive Behavior/psychology , Magnetic Resonance Imaging , Male , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/drug effects , Psychiatric Status Rating Scales , Radionuclide Imaging , Radiopharmaceuticals
3.
CNS Spectr ; 8(10): 763-70, 2003 Oct.
Article in English | MEDLINE | ID: mdl-14712174

ABSTRACT

BACKGROUND: This study examined the relationship of self-reported histories of childhood trauma to measures of affective instability in a sample of unmedicated outpatients with various personality disorders (n=174). METHODS: Childhood trauma was measured by the Childhood Trauma Questionnaire. Affective instability comprises at least two dimensions: affective lability, assessed using the Affective Lability Scale, and affective intensity, assessed using the Affective Intensity Measure. RESULTS: A history of emotional abuse was the only trauma variable that significantly correlated with the affect measures in the total sample (r=.21-.30). More fine-grained analyses revealed that the relationship of emotional abuse and affective instability measures varied as a function of both gender and personality disorder type. In subjects with borderline personality disorder, the correlation for emotional abuse was greatly attenuated for both Affective Lability Scale (r=.10) and Affective Intensity Measure (r=.15) total scores. CONCLUSION: This suggests that nontrauma-related factors may be more predominant in affective dyscontrol in individuals with borderline personality disorder.


Subject(s)
Child Abuse/psychology , Child Abuse/statistics & numerical data , Mood Disorders/epidemiology , Mood Disorders/etiology , Personality Disorders/epidemiology , Personality Disorders/etiology , Adolescent , Adult , Female , Humans , Male , Middle Aged , Surveys and Questionnaires
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