Schaeffer Sofia, Bogdanovic Andrijana, Hildebrandt Talitha, Flint Emilio, Geng Anne, Pecenko Sylvia, Lussier Paul, Strumberger Michael A, Meyer Martin, Weber Jakob, Heim Markus H, Cajochen Christian, Bernsmeier Christine
Department of Biomedicine and Department of Clinical Research, University of Basel, Basel, Switzerland.
University Centre for Gastrointestinal and Liver Diseases, Basel, Switzerland.
Front Netw Physiol. 2024 Dec 4;4:1458665. doi: 10.3389/fnetp.2024.1458665. eCollection 2024.
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, = 0.0036), longer wakefulness after sleep onset (MASLD vs. HC 45.4 min vs. 21.3 min, = 0.0004), and decreased sleep efficiency (MASLD vs. HC 86.5% vs. 92.8%, = 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, = 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.
代谢功能障碍相关脂肪性肝病(MASLD)是一种多系统疾病,其发病机制多因素,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额外影响其发展,因为它会影响包括肝脏在内的多个器官的代谢。此外,睡眠问卷数据证明MASLD患者存在睡眠-觉醒中断。我们使用活动记录仪对35例经活检证实的MASLD患者和16例健康对照(HC)进行了为期4周的全天24小时监测,以客观评估其睡眠-觉醒节律。为了重新调整睡眠节律,在2周后进行了一次标准化的睡眠卫生教育课程。活动记录仪数据显示,与HC相比,MASLD患者每晚觉醒次数更多(MASLD组与HC组分别为8.5次与5.5次,P = 0.0036),睡眠开始后的清醒时间更长(MASLD组与HC组分别为45.4分钟与21.3分钟,P = 0.0004),睡眠效率降低(MASLD组与HC组分别为86.5%与92.8%,P = 0.0008),尽管睡眠时间相当。MASLD患者自我报告睡眠时间较短(MASLD组与HC组分别为6小时与6小时45分钟,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并未使睡眠参数产生显著变化。我们的研究结果表明,MASLD患者夜间睡眠碎片化,其特征是清醒时间增加和睡眠效率降低,主观上感觉睡眠时间缩短和入睡延迟。单次睡眠卫生教育课程并未改善睡眠参数。