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杜兴氏肌肉营养不良症中与年龄相关的睡眠纺锤波特征

Age-associated sleep spindle characteristics in Duchenne muscular dystrophy.

作者信息

Simon Katharine C, Cadle Chelsea, Nakra Neal, Nagel Marni C, Malerba Paola

机构信息

Department of Pediatrics, School of Medicine, University of California, Irvine, Irvine, CA, USA.

Pulmonology Department, Children's Hospital of Orange County, Orange, CA, USA.

出版信息

Sleep Adv. 2024 Mar 14;5(1):zpae015. doi: 10.1093/sleepadvances/zpae015. eCollection 2024.

Abstract

Brain oscillations of non-rapid eye movement sleep, including slow oscillations (SO, 0.5-1.5 Hz) and spindles (10-16 Hz), mirror underlying brain maturation across development and are associated with cognition. Hence, age-associated emergence and changes in the electrophysiological properties of these rhythms can lend insight into cortical development, specifically in comparisons between pediatric populations and typically developing peers. We previously evaluated age-associated changes in SOs in male patients with Duchenne muscular dystrophy (DMD), finding a significant age-related decline between 4 and 18 years. While primarily a muscle disorder, male patients with DMD can also have sleep, cognitive, and cortical abnormalities, thought to be driven by altered dystrophin expression in the brain. In this follow-up study, we characterized the age-associated changes in sleep spindles. We found that age-dependent spindle characteristics in patients with DMD, including density, frequency, amplitude, and duration, were consistent with age-associated trends reported in the literature for typically developing controls. Combined with our prior finding of age-associated decline in SOs, our results suggest that SOs, but not spindles, are a candidate intervention target to enhance sleep in patients with DMD.

摘要

非快速眼动睡眠的脑振荡,包括慢振荡(SO,0.5 - 1.5赫兹)和纺锤波(10 - 16赫兹),反映了整个发育过程中潜在的脑成熟情况,并与认知相关。因此,这些节律的电生理特性随年龄的出现和变化有助于深入了解皮层发育,特别是在儿科人群与正常发育的同龄人之间进行比较时。我们之前评估了杜氏肌营养不良症(DMD)男性患者中慢振荡随年龄的变化,发现4至18岁之间存在显著的年龄相关下降。虽然DMD主要是一种肌肉疾病,但DMD男性患者也可能有睡眠、认知和皮层异常,据认为这是由大脑中肌营养不良蛋白表达改变所驱动的。在这项后续研究中,我们描述了睡眠纺锤波随年龄的变化。我们发现,DMD患者中与年龄相关的纺锤波特征,包括密度、频率、幅度和持续时间,与文献中报道的正常发育对照的年龄相关趋势一致。结合我们之前发现的慢振荡随年龄下降的结果,我们的研究结果表明,慢振荡而非纺锤波,是改善DMD患者睡眠的一个候选干预靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa86/10960605/b9e79040ab0c/zpae015_fig1.jpg

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