Sleep oscillations and their relations with sleep-dependent memory consolidation in early course psychosis and first-degree relatives

IF 3.6 2区 医学 Q1 PSYCHIATRY Schizophrenia Research Pub Date : 2024-11-07 DOI:10.1016/j.schres.2024.10.026
Dan Denis , Bengi Baran , Dimitrios Mylonas , Courtney Spitzer , Nicolas Raymond , Christine Talbot , Erin Kohnke , Olivia Larson , Robert Stickgold , Matcheri Keshavan , Dara S. Manoach
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Abstract

Sleep spindles mediate sleep-dependent memory consolidation, particularly when coupled to neocortical slow oscillations (SOs). Schizophrenia is characterized by a deficit in sleep spindles that correlates with reduced overnight memory consolidation. Here, we examined sleep spindle activity, SO-spindle coupling, and both motor procedural and verbal declarative memory consolidation in early course, minimally medicated psychosis patients and non-psychotic first-degree relatives. Using a four-night experimental procedure, we observed significant deficits in spindle density and amplitude in patients relative to controls that were driven by individuals with schizophrenia. Schizophrenia patients also showed reduced sleep-dependent consolidation of motor procedural memory, which correlated with lower spindle density. Contrary to expectations, there were no group differences in the consolidation of declarative memory on a word pairs task. Nor did the relatives of patients differ in spindle activity or memory consolidation compared with controls, however increased consistency in the timing of SO-spindle coupling were seen in both patients and relatives. Our results extend prior work by demonstrating correlated deficits in sleep spindles and sleep-dependent motor procedural memory consolidation in early course, minimally medicated patients with schizophrenia, but not in first-degree relatives. This is consistent with other work in suggesting that impaired sleep-dependent memory consolidation has some specificity for schizophrenia and is a core feature rather than reflecting the effects of medication or chronicity.
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早期精神病和一级亲属的睡眠振荡及其与依赖睡眠的记忆巩固的关系。
睡眠棘介导依赖睡眠的记忆巩固,尤其是与新皮质慢振荡(SOs)结合时。精神分裂症的特征是睡眠纺锤体的缺失,而睡眠纺锤体的缺失与隔夜记忆巩固的减少有关。在这里,我们研究了病程早期、用药最少的精神病患者和非精神病患者一级亲属的睡眠主轴活动、SO-主轴耦合以及运动程序性记忆和言语陈述性记忆的巩固。通过四晚的实验过程,我们观察到相对于对照组,精神分裂症患者的纺锤体密度和振幅明显不足。精神分裂症患者还表现出依赖睡眠的运动程序记忆巩固能力下降,这与纺锤体密度较低有关。与预期相反的是,在单词配对任务中,陈述性记忆的巩固并无群体差异。与对照组相比,患者亲属在纺锤体活动或记忆巩固方面也没有差异,但在患者和亲属中,SO-纺锤体耦合的时间一致性都有所提高。我们的研究结果扩展了之前的研究,证明了早期精神分裂症患者在睡眠纺锤体和依赖睡眠的运动程序记忆巩固方面存在相关缺陷,而一级亲属中却没有这种缺陷。这与其他研究结果一致,表明依赖睡眠的记忆巩固功能受损对精神分裂症有一定的特异性,是精神分裂症的核心特征,而不是反映药物或慢性病的影响。
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来源期刊
Schizophrenia Research
Schizophrenia Research 医学-精神病学
CiteScore
7.50
自引率
8.90%
发文量
429
审稿时长
10.2 weeks
期刊介绍: As official journal of the Schizophrenia International Research Society (SIRS) Schizophrenia Research is THE journal of choice for international researchers and clinicians to share their work with the global schizophrenia research community. More than 6000 institutes have online or print (or both) access to this journal - the largest specialist journal in the field, with the largest readership! Schizophrenia Research''s time to first decision is as fast as 6 weeks and its publishing speed is as fast as 4 weeks until online publication (corrected proof/Article in Press) after acceptance and 14 weeks from acceptance until publication in a printed issue. The journal publishes novel papers that really contribute to understanding the biology and treatment of schizophrenic disorders; Schizophrenia Research brings together biological, clinical and psychological research in order to stimulate the synthesis of findings from all disciplines involved in improving patient outcomes in schizophrenia.
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