Central dopaminergic transmission appears to be involved in the expression of some schizophrenic symptoms. However, elucidation of the role of dopamine (DA) in schizophrenia has eluded investigative efforts partially because no accurate and easily repeatable measure of brain DA activity exists. The development of a technique to measure homovanillic acid in plasma(pHVA) has offered the possibility of performing serial measurements of this major DA metabolite. Results to date suggest that pHVA concentrations are lower in chronic schizophrenic patients compared to normal controls, and that pHVA values correlate with schizophrenic symptom severity. In addition, pHVA levels were shown to initially rise and subsequently decline during chronic neuroleptic administration in treatment responsive but not in treatment refractory schizophrenic patients. Studies contained in this proposal are focused on elaborating upon the relationship between schizophrenic symptoms, neuroleptic drugs and DA turnover as reflected by pHVA concentrations. Schizophrenic symptoms and pHVA concentrations will be assessed during 5 weeks of administration of the """"""""typical"""""""" neuroleptic drug haloperidol. Those schizophrenic patients who fail to benefit from haloperidol treatment will be treated with the """"""""atypical"""""""" neuroleptic Clozapine for 6 weeks and severity of schizophrenic symptoms and pHVA will be assessed. Changes in pHVA concentrations during neuroleptic administration, both typical and atypical, will be compared between schizophrenic patients who benefit from treatment with haloperidol, patients who are refractory to haloperidol but benefit from treatment with clozapine and schizophrenic patients who are refractory to both types of drugs. Also included in the application is a separate study that examines the use of pHVA measurement to predict clinical treatment response in a naturalistic manner.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH037922-08
Application #
3376415
Study Section
Psychopathology and Clinical Biology Research Review Committee (PCB)
Project Start
1989-09-01
Project End
1993-08-31
Budget Start
1991-09-01
Budget End
1992-08-31
Support Year
8
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Mount Sinai School of Medicine
Department
Type
Schools of Medicine
DUNS #
City
New York
State
NY
Country
United States
Zip Code
10029
Serper, M R; Davidson, M; Harvey, P D (1994) Attentional predictors of clinical change during neuroleptic treatment in schizophrenia. Schizophr Res 13:65-71
Stern, R G; Kahn, R S; Davidson, M et al. (1994) Early response to clozapine in schizophrenia. Am J Psychiatry 151:1817-8
Davidson, M; Kahn, R S; Stern, R G et al. (1993) Treatment with clozapine and its effect on plasma homovanillic acid and norepinephrine concentrations in schizophrenia. Psychiatry Res 46:151-63
Stern, R G; Kahn, R S; Harvey, P D et al. (1993) Early response to haloperidol treatment in chronic schizophrenia. Schizophr Res 10:165-71
Kahn, R S; Davidson, M; Hirschowitz, J et al. (1992) Nocturnal growth hormone secretion in schizophrenic patients and healthy subjects. Psychiatry Res 41:155-61
Keefe, R S; Lobel, D S; Mohs, R C et al. (1991) Diagnostic issues in chronic schizophrenia: kraepelinian schizophrenia, undifferentiated schizophrenia, and state-independent negative symptoms. Schizophr Res 4:71-9
Harvey, P D; Davidson, M; Powchik, P et al. (1991) Time course and clinical predictors of treatment response in schizophrenia. Schizophr Res 5:161-6
Davis, K L; Kahn, R S; Ko, G et al. (1991) Dopamine in schizophrenia: a review and reconceptualization. Am J Psychiatry 148:1474-86
Davidson, M; Kahn, R S; Knott, P et al. (1991) Effects of neuroleptic treatment on symptoms of schizophrenia and plasma homovanillic acid concentrations. Arch Gen Psychiatry 48:910-3
Harvey, P D; Putnam, K M; Davidson, M et al. (1991) Brief neuroleptic discontinuation and clinical symptoms in Kraepelinian and non-Kraepelinian chronic schizophrenic patients. Psychiatry Res 38:285-92

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