Schlosser Danielle A, Fisher Melissa, Gard David, Fulford Daniel, Loewy Rachel L, Vinogradov Sophia
University of California at San Francisco, San Francisco, CA, USA.
University of California at San Francisco, San Francisco, CA, USA; San Francisco Department of Veterans Affairs Medical Center, San Francisco, CA, USA.
Schizophr Res. 2014 Sep;158(1-3):52-7. doi: 10.1016/j.schres.2014.06.024. Epub 2014 Jul 5.
Motivational impairment is a critical factor that contributes to functional disability in schizophrenia and undermines an individual's ability to engage in and adhere to effective treatment. However, little is known about the developmental trajectory of deficits in motivation and whether these deficits are present prior to the onset of psychosis. We assessed several components of motivation including anticipatory versus consummatory pleasure (using the Temporal Experience of Pleasure Scale (TEPS)), and behavioral drive, behavioral inhibition, and reward responsivity (using the Behavioral Inhibition Scale/Behavioral Activation Scale (BIS/BAS)). A total of 234 participants completed study measures, including 60 clinical high risk (CHR) participants, 60 recent-onset schizophrenia participants (RO), 78 chronic schizophrenia participants (SZ) and 29 healthy controls (HC) age matched to the CHR group. CHR participants endorsed greater deficits in anticipatory pleasure and reward responsivity, relative to HC comparison participants and individuals diagnosed with schizophrenia. Motivational deficits were not more pronounced over the course of illness. Depressed mood was uniquely associated with impairments in motivation in the CHR sample, but not the schizophrenia participants. The results suggest that CHR individuals experience multiple contributors to impaired motivation, and thus multiple leverage points for treatment.
动机障碍是导致精神分裂症功能残疾的关键因素,会削弱个体参与并坚持有效治疗的能力。然而,对于动机缺陷的发展轨迹以及这些缺陷在精神病发作之前是否存在,我们知之甚少。我们评估了动机的几个组成部分,包括预期性愉悦与满足性愉悦(使用愉悦时间体验量表(TEPS)),以及行为驱动力、行为抑制和奖励反应性(使用行为抑制量表/行为激活量表(BIS/BAS))。共有234名参与者完成了研究测量,其中包括60名临床高危(CHR)参与者、60名近期发病的精神分裂症参与者(RO)、78名慢性精神分裂症参与者(SZ)以及29名与CHR组年龄匹配的健康对照者(HC)。与HC对照参与者和被诊断为精神分裂症的个体相比,CHR参与者在预期性愉悦和奖励反应性方面的缺陷更为明显。在疾病过程中,动机缺陷并没有更加明显。在CHR样本中,抑郁情绪与动机受损存在独特关联,但在精神分裂症参与者中并非如此。结果表明,CHR个体经历了多种导致动机受损的因素,因此有多个治疗切入点。