Subjective experience and D2 receptor occupancy in patients with recent-onset schizophrenia treated with low-dose olanzapine or haloperidol:: A randomized, double-blind study

被引:104
作者
de Haan, L [1 ]
van Bruggen, M [1 ]
Lavalaye, J [1 ]
Booij, J [1 ]
Dingemans, PMAJ [1 ]
Linszen, D [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Dept Psychiat, NL-1100 DE Amsterdam, Netherlands
关键词
D O I
10.1176/appi.ajp.160.2.303
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
objective: The authors tested the hypothesis that a dopamine D-2 receptor Occupancy level between 60% and 70% in patients with recent-onset schizophrenia would result in optimal subjective experience. in addition, they sought preliminary evidence on whether subjective experience is better with low-dose olanzapine than with low-dose haloperidol. Method: Subjects (N=24) who met DSM-IV criteria for schizophrenia were randomly assigned to 6 weeks of double-blind treatment with either olanzapine, 7.5 mg/day, or haloperidol, 2.5 mg/day. Subjective experience, psychopathology, and extrapyramidal symptoms were assessed at baseline and at endpoint. After 6 weeks, D-2 receptor occupancy was assessed with [I-123]iodobenzamide single photon emission computed tomography. Results: The two study groups were similar at baseline. After 6 weeks, patients receiving olanzapine had a significantly lower mean dopamine D-2 receptor occupancy (51.0%, range=36%-67%) than those given halopericlol (65.5%, range=45%-75%). Receptor occupancy between 60% and 70% was associated with optimal subjective experience, and subjective experience improved significantly in the haloperidol group. Conclusions: A level of D-2 receptor occupancy between 60% and 70% is optimal for subjective experience of patients with recent-onset schizophrenia. Substantial interindividual variation in D-2 receptor occupancy was seen at fixed low-dose levels of olanzapine and halopericlol. Olanzapine, 7.5 mg/day, showed no superior subjective response over halopericlol, 2.5 mg/day. Olanzapine may need to be dosed higher than 7.5 mg/day for most patients with recent-onset schizophrenia, and halopericlol needs to be individually titrated in the very low dose range to reach optimal occupancy.
引用
收藏
页码:303 / 309
页数:7
相关论文
共 33 条
[1]   ANTIPSYCHOTIC-DRUGS - IS MORE WORSE - A METAANALYSIS OF THE PUBLISHED RANDOMIZED CONTROL TRIALS [J].
BOLLINI, P ;
PAMPALLONA, S ;
ORZA, MJ ;
ADAMS, ME ;
CHALMERS, TC .
PSYCHOLOGICAL MEDICINE, 1994, 24 (02) :307-316
[2]   Striatal D2 blockade and depression in schizophrenia -: SPET findings [J].
Bressan, RA ;
Mulligan, RS ;
Costa, DC ;
Jones, HM ;
Ell, PJ ;
Kerwin, RW ;
Pilowsky, LS .
BIOLOGICAL PSYCHIATRY, 2000, 47 (08) :128S-128S
[3]   Dopamine D2 receptor blockade in schizophrenia [J].
Bressan, RA ;
Jones, HM ;
Ell, PJ ;
Pilowsky, LS .
AMERICAN JOURNAL OF PSYCHIATRY, 2001, 158 (06) :971-972
[4]  
BUIS W, 1992, AM J PSYCHIAT, V149, P844
[5]   Subjective experience and striatal dopamine D2 receptor occupancy in patients with schizophrenia stabilized by olanzapine or risperidone [J].
de Haan, L ;
Lavalaye, J ;
Linszen, D ;
Dingemans, PMAJ ;
Booij, J .
AMERICAN JOURNAL OF PSYCHIATRY, 2000, 157 (06) :1019-1020
[6]   Psychometric properties of the Subjective Well-Being Under Neuroleptics Scale and the Subjective Deficit Syndrome Scale [J].
de Haan, L ;
Weisfelt, M ;
Dingemans, PMAJ ;
Linszen, DH ;
Wouters, L .
PSYCHOPHARMACOLOGY, 2002, 162 (01) :24-28
[7]   A PET study of [C-11]FLB 457 binding to extrastriatal D-2-dopamine receptors in healthy subjects and antipsychotic drug-treated patients [J].
Farde, L ;
Suhara, T ;
Nyberg, S ;
Karlsson, P ;
Nakashima, Y ;
Hietala, J ;
Halldin, C .
PSYCHOPHARMACOLOGY, 1997, 133 (04) :396-404
[8]   QUANTITATIVE-ANALYSIS OF D2 DOPAMINE RECEPTOR-BINDING IN THE LIVING HUMAN-BRAIN BY PET [J].
FARDE, L ;
HALL, H ;
EHRIN, E ;
SEDVALL, G .
SCIENCE, 1986, 231 (4735) :258-261
[9]   Conventional versus atypical neuroleptics: Subjective quality of life in schizophrenic patients [J].
Franz, M ;
Lis, S ;
Pluddemann, K ;
Gallhofer, B .
BRITISH JOURNAL OF PSYCHIATRY, 1997, 170 :422-425
[10]  
HAASE HJ, 1961, SYSTEME EXTRAPYRAMID, P329