Department of Physical Therapy, The Stanley Steyer School of Health Professions, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel; Department of Psychiatry, University of Cambridge, Cambridge, UK; and Cambridgeshire and Peterborough NHS Foundation Trust, Fulbourn Hospital, Fulbourn, Cambridge, UK.
Department of Psychiatry, University of Cambridge, Cambridge, UK.
Br J Psychiatry. 2023 Jul;223(1):295-297. doi: 10.1192/bjp.2022.191.
Negative symptoms of schizophrenia manifest as reduced motivation and pleasure (MAP) and impaired emotional expressivity (EXP). These can occur as primary phenomena, but have also been suggested to occur secondary to other clinical factors, including antipsychotic-induced sedation. However, this relationship has not been established formally. Here, we examined the effect of antipsychotic-induced sedation (assessed via the proxy of total daily sleep duration) on MAP and EXP in a cohort of 187 clozapine-treated patients with schizophrenia followed for over 2 years on average, using multilevel regression and mediation models. MAP, but not EXP, was adversely influenced by sedation, independently of the severity of psychosis or depression. Moreover, clozapine impaired MAP indirectly by worsening sedation, but after accounting for clozapine-induced sedation, clozapine improved MAP. Our results highlight the importance of addressing sedative side-effects of antipsychotics to improve clinical outcomes.
精神分裂症的阴性症状表现为动机和快感降低(MAP)和情感表达能力受损(EXP)。这些症状可能是原发性的,但也有人认为它们是继发于其他临床因素,包括抗精神病药引起的镇静作用。然而,这种关系尚未得到正式确立。在这里,我们使用多层次回归和中介模型,检查了抗精神病药引起的镇静作用(通过总每日睡眠时间的代理指标评估)对 187 名接受氯氮平治疗的精神分裂症患者的 MAP 和 EXP 的影响,这些患者平均随访超过 2 年。MAP 而不是 EXP,独立于精神病或抑郁的严重程度,受到镇静作用的不利影响。此外,氯氮平通过加重镇静作用间接损害 MAP,但在考虑氯氮平引起的镇静作用后,氯氮平改善了 MAP。我们的研究结果强调了解决抗精神病药镇静副作用以改善临床结局的重要性。