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A 4-year dopamine transporter (DAT) imaging study in neuroleptic-naive first episode schizophrenia patients
Authors:Anna Mané  ,Judith GallegoFrancisco Lomeñ  a,Jose Javier MateosEmilio Fernandez-Egea,Guillermo Horga,Albert Cot,Javier Pavia,Miguel Bernardo,Eduard Parellada
Affiliation:
  • a Departament de Psiquiatria, Centre Fòrum Hospital del Mar, Barcelona, Spain
  • b Departament de Biofísica, Universitat de Barcelona, Barcelona, Spain
  • c Medicina Nuclear, Institut de Diagnòstic per la Imatge, Hospital Clínic, Barcelona, Spain
  • d Institut d''Investigacions Biomèdiques Augusti Pi i Sunyer (IDIBAPS), Barcelona, Spain
  • e Programa Esquizofrenia Clinic, Departament de Psiquiatria, Institut de Neurociencies, Hospital Clínic, Barcelona, Spain
  • f Centre de Diagnòstic per la Imatge, Barcelona, Spain
  • g Department of Psychiatry, University of Cambridge, Cambridge, United Kingdom
  • h Cambridge and Peterborough NHS Foundation Trust, Cambridge, United Kingdom
  • i Brain Imaging Laboratory, Division of Child and Adolescent Psychiatry, Columbia University, New York, NY, USA
  • j Centro de Investigación Nacional en Red en Bioingeniería, Biomateriales y Nanomedicina, CIBER-BBN, Barcelona, Spain
  • k Hospital Clínic de Barcelona, Institut de Neurociències, Barcelona, Spain
  • l Centro de Investigación Biomédica en Red de Salud Mental, CIBERSAM, Barcelona, Spain
  • Abstract:Alterations in the dopaminergic system have long been implicated in schizophrenia. A key component in dopaminergic neurotransmission is the striatal dopamine transporter (DAT). To date, there have been no longitudinal studies evaluating the course of DAT in schizophrenia. A 4-year follow-up study was therefore conducted in which single photon emission computed tomography was used to measure DAT binding in 14 patients and 7 controls. We compared the difference over time in [123I] FP-CIT striatal/occipital uptake ratios (SOUR) between patients and controls and the relationship between this difference and both symptomatology and functional outcome at follow-up. We also calculated the relationship between baseline SOUR, symptoms and functional outcome at follow-up. There were no statistically significant differences between patients' SOUR changes over time and those of controls. A significant negative correlation was observed between patients' SOUR changes over time and negative symptomatology at follow-up. A significant negative correlation was also found between baseline SOUR in patients and negative symptomatology, and there was a significant association between lower SOUR at baseline and poor outcome. Although the study found no overall differences in DAT binding during follow-up between schizophrenia patients and controls, it demonstrated that differences in DAT binding relate to patients' characteristics at follow-up.
    Keywords:Basal ganglia   Outcome   Negative   Longitudinal
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