Correlation between plasma homovanillic acid levels and the response to atypical antipsychotics in male patients with schizophrenia

被引:3
|
作者
Kaneda, Y
Kawamura, I
Ohmori, T
机构
[1] Tokushima Univ Hosp, Dept Psychiat, Tokushima 7708503, Japan
[2] Fujii Hosp, Dept Neuropsychiat, Fuji, Shizuoka, Japan
关键词
atypical antipsychotic agents; olanzapine; perospirone; plasma homovanillic acid; quetiapine;
D O I
10.1097/01.wnf.0000192138.53769.43
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: The authors investigated the effects of atypical antipsychotic drugs-olanzapine, perospirone, and quetiapine-on plasma homovanillic acid (pHVA) in male patients with chronic schizophrenia. Methods: In this prospective, open-label study, the subjects were 30 inpatients who were diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders, 4th edition, criteria for schizophrenia. The authors switched patients from typical antipsychotic drugs to olanzapine, perospirone, or quetiapine. Each patient gave informed consent for the research. pHVA was assessed before and after switching medications. Results: After the switch, the authors found a significant improvement in psychotic symptoms, nonsignificant improvement in extrapyramidal symptoms, and a nonsignificant reduction in pHVA. In addition, the baseline pHVA correlated positively with the score changes from baseline in the Brief Psychiatric Rating Scale (BPRS) total, positive, and negative symptoms in the group with a whole sample and in the olanzapine-treated group, and with the score changes in the BPRS total and positive symptoms in the quetiapine-treated group. Conclusion: Our findings indicated that the preswitching pHVA levels could be used to predict changes in the psychotic symptoms of male patients with chronic schizophrenia when switching to atypical antipsychotic drugs.
引用
收藏
页码:262 / 264
页数:3
相关论文
共 50 条
  • [1] The effects of typical antipsychotic replacement by atypical antipsychotics on plasma homovanillic acid levels in male patients with chronic schizophrenia
    Kaneda, Y
    Fujii, A
    Ohmori, T
    INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 2005, 20 (03) : A7 - A7
  • [2] Plasma homovanillic acid levels in schizophrenic patients:: Correlation with negative symptoms
    Davila, Ricardo
    Zumarraga, Mercedes
    Basterreche, Nieves
    Arrue, Aurora
    Anguiano, Juan B.
    PSYCHIATRY RESEARCH, 2007, 151 (1-2) : 163 - 168
  • [3] PLASMA HOMOVANILLIC-ACID LEVELS AND SUBTYPING OF SCHIZOPHRENIA
    CHANG, WH
    CHEN, TY
    LEE, CF
    HUNG, JC
    HU, WH
    YEH, EK
    PSYCHIATRY RESEARCH, 1988, 23 (03) : 239 - 244
  • [4] EFFECT OF TYPICAL AND ATYPICAL ANTIPSYCHOTICS ON PLASMA PROLACTIN LEVELS IN SCHIZOPHRENIA
    Bilal, Muhammad Sami
    Rana, Mowadat Hussain
    GOMAL JOURNAL OF MEDICAL SCIENCES, 2014, 12 (03): : 142 - 146
  • [5] PLASMA HOMOVANILLIC-ACID AND DRUG RESPONSE IN SCHIZOPHRENIA
    DIAMOND, BI
    ONEAL, E
    WANG, J
    BORISON, RL
    SCHIZOPHRENIA RESEARCH, 1991, 4 (03) : 343 - 344
  • [6] Plasma levels of homovanillic acid and the response to risperidone in first episode untreated acute schizophrenia
    Yoshimura, R
    Ueda, N
    Shinkai, K
    Nakamura, J
    INTERNATIONAL CLINICAL PSYCHOPHARMACOLOGY, 2003, 18 (02) : 107 - 111
  • [7] Plasma homovanillic acid in schizophrenia
    Freedman, R
    SCHIZOPHRENIA BULLETIN, 2005, 31 (02) : 288 - 289
  • [8] CIRCADIAN VARIATION OF PLASMA HOMOVANILLIC-ACID LEVELS IS ATTENUATED BY FLUPHENAZINE IN PATIENTS WITH SCHIZOPHRENIA
    DORAN, AR
    LABARCA, R
    WOLKOWITZ, OM
    ROY, A
    DOUILLET, P
    PICKAR, D
    ARCHIVES OF GENERAL PSYCHIATRY, 1990, 47 (06) : 558 - 563
  • [9] PLASMA HOMOVANILLIC-ACID LEVELS IN FIRST-EPISODE SCHIZOPHRENIA - PSYCHOPATHOLOGY AND TREATMENT RESPONSE
    KOREEN, AR
    LIEBERMAN, J
    ALVIR, J
    MAYERHOFF, D
    LOEBEL, A
    CHAKOS, M
    AMIN, F
    COOPER, T
    ARCHIVES OF GENERAL PSYCHIATRY, 1994, 51 (02) : 132 - 138
  • [10] Dose Response and Atypical Antipsychotics in Schizophrenia
    Bruce J. Kinon
    Jonna Ahl
    Virginia L. Stauffer
    Angela L. Hill
    Peter F. Buckley
    CNS Drugs, 2004, 18 : 597 - 616