Effect of a haloperidol challenge on regional brain metabolism in neuroleptic-responsive and nonresponsive schizophrenic patients

被引:49
作者
Bartlett, EJ
Brodie, JD
Simkowitz, P
Schlosser, R
Dewey, SL
Lindenmayer, JP
Rusinek, H
Wolkin, A
Cancro, R
Schiffer, W
机构
[1] NYU, Med Ctr, Dept Psychiat, New York, NY 10016 USA
[2] NYU, Med Ctr, Dept Radiol, New York, NY 10016 USA
[3] Brookhaven Natl Lab, Dept Chem, Upton, NY 11973 USA
关键词
D O I
10.1176/ajp.155.3.337
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: The CNS metabolic response to a neuroleptic challenge in treatment-responsive and nonresponsive schizophrenic patients was measured in order to examine the relation between treatment outcome and the capacity to alter neurochemical function in response to acute receptor blockade. Method: Positron emission tomography (PET) and [F-18]fluorodeoxyglucose (FDG) were used to measure regional cerebral metabolism in seven schizophrenic patients judged to have been responsive to drug treatment previously and seven nonresponsive schizophrenic patients after a drug-free period of at least 3 weeks (baseline) and again 12 hours after administration of 5.0 mg of haloperidol. Results: The haloperidol challenge caused widespread decreases in absolute metabolism in the nonresponsive patients but not the responsive patients. These group differences reflect the findings on the second (challenge) scans, since metabolic values at baseline were not statistically different in the two groups. The pattern of decreased metabolic activity in the nonresponders after the haloperidol challenge is similar to that previously observed in normal subjects. Conclusions: The metabolic response to drug challenge separates treatment responders from nonresponders and normal subjects. The results suggest that subtyping of schizophrenia (and other psychiatric disorders) can be achieved by measuring the physiologic response to a pharmacologic challenge in vivo with chemical brain-imaging techniques.
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页码:337 / 343
页数:7
相关论文
共 30 条
[1]  
ALEXANDER GE, 1990, PROG BRAIN RES, V85, P119
[2]   Schizophrenia and cognitive dysmetria: A positron-emission tomography study of dysfunctional prefrontal-thalamic-cerebellar circuitry [J].
Andreasen, NC ;
OLeary, DS ;
Cizadlo, T ;
Arndt, S ;
Rezai, K ;
Ponto, LLB ;
Watkins, GL ;
Hichwa, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (18) :9985-9990
[3]  
BARTLETT EJ, 1994, AM J PSYCHIAT, V151, P681
[4]   Time-dependent effects of a haloperidol challenge on energy metabolism in the normal human brain [J].
Bartlett, EJ ;
Brodie, JD ;
Simkowitz, P ;
Dewey, SL ;
Rusinek, H ;
Volkow, ND ;
Wolf, AP ;
Smith, G ;
Wolkin, A ;
Cancro, R .
PSYCHIATRY RESEARCH, 1996, 60 (2-3) :91-99
[5]   Neurocognitive impairment in schizophrenia and how it affects treatment options [J].
Bilder, RM .
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE, 1997, 42 (03) :255-264
[6]   Schizophrenia is associated with elevated amphetamine-induced synaptic dopamine concentrations: Evidence from a novel positron emission tomography method [J].
Breier, A ;
Su, TP ;
Saunders, R ;
Carson, RE ;
Kolachana, BS ;
de Bartolomeis, A ;
Weinberger, DR ;
Weisenfeld, N ;
Malhotra, AK ;
Eckelman, WC ;
Pickar, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2569-2574
[7]  
Brodie JD, 1996, AM J PSYCHIAT, V153, P145
[8]  
BUCHSBAUM MS, 1992, NEUROPSYCHOPHARMACOL, V6, P155
[9]  
BUCHSBAUM MS, 1992, ARCH GEN PSYCHIAT, V49, P966
[10]   HIGH CENTRAL D2-DOPAMINE RECEPTOR OCCUPANCY AS ASSESSED WITH POSITRON EMISSION TOMOGRAPHY IN MEDICATED BUT THERAPY-RESISTANT SCHIZOPHRENIC-PATIENTS [J].
COPPENS, HJ ;
SLOOFF, CJ ;
PAANS, AMJ ;
WIEGMAN, T ;
VAALBURG, W ;
KORF, J .
BIOLOGICAL PSYCHIATRY, 1991, 29 (07) :629-634