
Am J Psychiatry 157:269-271, February 2000
© 2000 American Psychiatric Association
Striatal Dopamine Transporter Binding in Neuroleptic-Naive Patients With Schizophrenia Studied With Positron Emission Tomography
Aki Laakso, M.D., Ph.D.,
Harry Vilkman, M.D.,
Birgitta Alakare, M.D.,
Merja Haaparanta, M.Sc.,
Jörgen Bergman, M.Sc.,
Olof Solin, Ph.D.,
Jari Peurasaari, M.D.,
Viljo Räkköläinen, M.D., Ph.D.,
Erkka Syvälahti, M.D., Ph.D., and
Jarmo Hietala, M.D., Ph.D.
OBJECTIVE: Recent in vivo imaging studies indicate a dysregulated presynaptic function of the striatal dopaminergic system in patients with schizophrenia. To further explore the basis of this phenomenon, the authors studied brain dopamine transporter binding in vivo in patients with first-episode, never-medicated schizophrenia. METHOD: Nine patients with schizophrenia and nine healthy matched comparison subjects were recruited. Striatal dopamine transporter binding was measured with positron emission tomography and a specific dopamine transporter ligand, [18F]CFT, a radiolabeled form of 2ß-carbomethoxy-3ß-(4-fluorophenyl)tropane. RESULTS: Average caudate and putamen dopamine transporter binding potentials were almost identical in the patients and comparison subjects, but the patients lacked the right-left asymmetry of the caudate dopamine transporter binding seen in the comparison group. CONCLUSIONS: Average striatal dopamine transporter density is unaltered in neuroleptic-naive patients with schizophrenia. However, patients lack asymmetry in caudate dopamine transporter binding, which conforms with disrupted brain lateralization in this disorder.
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