Significant nocturnal wakefulness after sleep onset in metabolic dysfunction-associated steatotic liver disease.

Frontiers in network physiology Pub Date : 2024-12-04 eCollection Date: 2024-01-01 DOI:10.3389/fnetp.2024.1458665
Sofia Schaeffer, Andrijana Bogdanovic, Talitha Hildebrandt, Emilio Flint, Anne Geng, Sylvia Pecenko, Paul Lussier, Michael A Strumberger, Martin Meyer, Jakob Weber, Markus H Heim, Christian Cajochen, Christine Bernsmeier
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Abstract

Metabolic dysfunction-associated steatotic liver disease (MASLD) is a multisystemic disease with a multifactorial pathogenesis involving dietary, environmental, and genetic factors. Previous mouse models suggested that circadian misalignment may additionally influence its development as it influences metabolism in diverse organs including the liver. Further, data from sleep questionnaires proved sleep-wake disruption in patients with MASLD. We objectively assessed sleep-wake rhythms in patients with biopsy-proven MASLD (n = 35) and healthy controls (HC, n = 16) using actigraphy 24/7 for 4 weeks. With the aim to re-align sleep rhythms a single standardized sleep hygiene education session was performed after 2 weeks. Actigraphy data revealed that MASLD patients had more awakenings per night (MASLD vs. HC 8.5 vs. 5.5, p = 0.0036), longer wakefulness after sleep onset (MASLD vs. HC 45.4 min vs. 21.3 min, p = 0.0004), and decreased sleep efficiency (MASLD vs. HC 86.5% vs. 92.8%, p = 0.0008) compared with HC despite comparable sleep duration. Patients with MASLD self-reported shorter sleep duration (MASLD vs. HC 6 h vs. 6 h 45 min, p = 0.01) and prolonged sleep latency contributing to poorer sleep quality. Standardized sleep hygiene education did not produce significant changes in sleep parameters. Our findings indicate fragmented nocturnal sleep in patients with MASLD, characterized by increased wakefulness and reduced sleep efficiency, perceived subjectively as shortened sleep duration and delayed onset. A single sleep hygiene education session did not improve sleep parameters.

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代谢功能障碍相关脂肪变性肝病患者睡眠后明显的夜间觉醒
代谢功能障碍相关脂肪变性肝病(MASLD)是一种多系统疾病,其发病机制涉及饮食、环境和遗传因素。先前的小鼠模型表明,昼夜节律失调可能会影响其发育,因为它会影响包括肝脏在内的多种器官的代谢。此外,来自睡眠问卷的数据证实了MASLD患者的睡眠-觉醒中断。我们客观地评估了活检证实的MASLD患者(n = 35)和健康对照(HC, n = 16)的睡眠-觉醒节律,使用活动记录仪24/7持续4周。为了重新调整睡眠节奏,两周后进行一次标准化的睡眠卫生教育。活动记录法数据显示,与HC相比,MASLD患者每晚醒来次数更多(MASLD vs. HC 8.5 vs. 5.5, p = 0.0036),睡眠开始后清醒时间更长(MASLD vs. HC 45.4 min vs. 21.3 min, p = 0.0004),睡眠效率下降(MASLD vs. HC 86.5% vs. 92.8%, p = 0.0008),尽管睡眠时间相当。MASLD患者自我报告的睡眠时间较短(MASLD vs. HC 6 h vs. 6 h 45 min, p = 0.01),睡眠潜伏期延长,导致睡眠质量较差。标准化的睡眠卫生教育未对睡眠参数产生显著影响。我们的研究结果表明,MASLD患者的夜间睡眠片段化,其特征是觉醒增加和睡眠效率降低,主观上被认为是睡眠时间缩短和发病延迟。单次睡眠卫生教育并没有改善睡眠参数。
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