Center for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Mental Health Center Glostrup, Glostrup, Denmark.
Center for Neuropsychiatric Schizophrenia Research (CNSR) and Center for Clinical Intervention and Neuropsychiatric Schizophrenia Research (CINS), Mental Health Center Glostrup, Glostrup, Denmark; Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Functional Imaging Unit, Department of Clinical Physiology, Nuclear Medicine and PET, Rigshospitalet Glostrup, University of Copenhagen, Rigshospitalet, Glostrup, Denmark.
Psychiatry Res. 2023 Aug;326:115308. doi: 10.1016/j.psychres.2023.115308. Epub 2023 Jun 17.
Aberrant neuronal coding of reward processing has been linked to psychosis. It remains unresolved how treatment with a partial dopamine agonist affects reward processing, and whether treatment affects reward processing differently in patients responding and not responding to treatment. Here, 33 antipsychotic-naïve psychosis patients and 33 matched healthy controls underwent functional magnetic resonance imaging before and after patients received aripiprazole monotherapy for six weeks. Processing of motivational salient events and negative outcome evaluation (NOE) was examined using a monetary incentive delay task. Psychopathology was assessed with the Positive and Negative Syndrome Scale, and responders were identified by having ≥30% reduction in positive symptoms (N=21). At baseline, patients displayed an increased NOE signal in the caudate and dorsolateral prefrontal cortex compared to healthy controls. In the caudate, the NOE signal was normalized at follow-up, and normalization was driven by responders. In responders only, there was a significant improvement in the motivational salience signal in the caudate at follow-up. Motivational salience and NOE signals in the caudate may be associated with a dopaminergic mechanism in patients characterized as responders which may not be the case in non-responders. Likewise, non-dopaminergic mechanism may underly abnormal NOE processing in dorsolateral prefrontal cortex.
异常的神经元编码奖励处理与精神病有关。目前尚不清楚多巴胺部分激动剂治疗如何影响奖励处理,以及治疗是否会对治疗有反应和无反应的患者的奖励处理产生不同的影响。在这里,33 名未经抗精神病药物治疗的精神病患者和 33 名匹配的健康对照组在接受阿立哌唑单药治疗 6 周前后接受了功能磁共振成像。使用货币奖励延迟任务检查了动机显着事件和负性结果评估 (NOE) 的处理。使用阳性和阴性综合征量表评估了精神病学,并且通过具有≥30%阳性症状减少来识别响应者(N=21)。在基线时,与健康对照组相比,患者的尾状核和背外侧前额叶皮层的 NOE 信号增加。在尾状核中,NOE 信号在随访时正常化,正常化是由响应者驱动的。仅在响应者中,尾状核中的动机显着性信号在随访时显著改善。尾状核中的动机显着性和 NOE 信号可能与以响应者为特征的患者中的多巴胺能机制有关,而在非响应者中则不然。同样,异常的 NOE 处理可能是背外侧前额叶皮层中的非多巴胺能机制。