Fervaha Gagan, Takeuchi Hiroyoshi, Lee Jimmy, Foussias George, Fletcher Paul J, Agid Ofer, Remington Gary
1] Schizophrenia Division, Centre for Addiction and Mental Health, Toronto, Canada [2] Institute of Medical Science, University of Toronto, Toronto, Canada.
1] Schizophrenia Division, Centre for Addiction and Mental Health, Toronto, Canada [2] Department of Psychiatry, University of Toronto, Toronto, Canada.
Neuropsychopharmacology. 2015 May;40(6):1539-48. doi: 10.1038/npp.2015.3. Epub 2015 Jan 8.
Antipsychotic drugs are thought to produce secondary negative symptoms, which can also exacerbate primary negative symptoms. In the present study, we examined whether motivational deficits in particular were related to antipsychotic treatment in patients with schizophrenia in a dose-dependent manner. Five hundred and twenty individuals with schizophrenia who were receiving antipsychotic monotherapy for at least 6 months and followed prospectively were included in the present study. Participants were receiving one of five antipsychotic medications (olanzapine, perphenazine, quetiapine, risperidone, or ziprasidone), and analyses were conducted for patients receiving each drug separately. Analysis of covariance models were constructed to examine the effect of antipsychotic dose on level of motivational impairment, controlling for selected demographic and clinical variables (eg, positive symptoms). Level of motivation, or deficits therein, were evaluated using a derived measure from the Quality of Life Scale, and in addition with scores derived from the Positive and Negative Syndrome Scale. Antipsychotic dose was not related to the level of amotivation for any of the medications examined. Moreover, severity of sedation was not significantly related to the degree of amotivation. One hundred and twenty-one individuals were identified as antipsychotic-free at baseline, and after 6 months of antipsychotic treatment, no change in motivation was found. Chronic treatment with antipsychotics does not necessarily impede or enhance goal-directed motivation in patients with schizophrenia. It is possible that the negative impact of antipsychotics in this regard is overstated; conversely, the present results also indicate that we must look beyond antipsychotics in our efforts to improve motivation.
抗精神病药物被认为会产生继发性阴性症状,这也会加重原发性阴性症状。在本研究中,我们检验了动机缺陷是否尤其以剂量依赖的方式与精神分裂症患者的抗精神病药物治疗相关。本研究纳入了520名接受抗精神病药物单一疗法至少6个月并进行前瞻性随访的精神分裂症患者。参与者正在服用五种抗精神病药物之一(奥氮平、奋乃静、喹硫平、利培酮或齐拉西酮),并对每种药物的患者分别进行分析。构建协方差分析模型以检验抗精神病药物剂量对动机损害水平的影响,并控制选定的人口统计学和临床变量(如阳性症状)。使用从生活质量量表衍生的指标,以及从阳性和阴性症状量表得出的分数来评估动机水平或其中的缺陷。抗精神病药物剂量与所检查的任何药物的无动机水平均无关联。此外,镇静严重程度与无动机程度无显著关联。121名个体在基线时被确定为未服用抗精神病药物,在接受6个月的抗精神病药物治疗后,未发现动机有变化。抗精神病药物的长期治疗不一定会阻碍或增强精神分裂症患者的目标导向动机。抗精神病药物在这方面的负面影响可能被夸大了;相反,目前的结果也表明,我们在努力改善动机时必须超越抗精神病药物的范畴。