Hendricks Jessie M, Metz Juriaan R, Boss H Myrthe, Collin Rob W J, de Vrieze Erik, van Wijk Erwin
Department of Otorhinolaryngology, Radboud University Medical Center, Nijmegen, The Netherlands.
Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
J Sleep Res. 2025 Aug;34(4):e14456. doi: 10.1111/jsr.14456. Epub 2024 Dec 30.
This study aimed to improve our understanding of sleep problems as a comorbidity of hereditary deaf-blindness due to Usher syndrome type 2a. Fifteen patients with Usher syndrome type 2a with a conclusive genetic diagnosis and 15 unaffected controls participated in comprehensive sleep and activity assessments for 2 weeks, using the MotionWatch 8 actigraph and consensus sleep diary. Various sleep parameters including sleep opportunity window, sleep latency, sleep efficiency, and self-reported sleep quality were analysed. Non-parametric circadian rhythm analysis was performed to evaluate circadian rhythmicity. Additionally, regression analyses were conducted to study potential correlations between sleep parameters and patients' demographics and disease progression. Patients with Usher syndrome type 2a exhibited significantly longer sleep latency and lower self-reported sleep and rest quality compared with controls. Additionally, day-to-day variability of sleep efficiency and sleep latency were significantly higher in the patient population. Non-parametric circadian rhythm analysis revealed no significant differences in circadian rhythmicity. Regression analyses indicated that having Usher syndrome type 2a was a significant predictor of poor sleep outcomes. No clear correlations were found between the level of visual impairment and sleep parameters, suggesting that the negative effects of Usher syndrome type 2a on sleep manifest independently of the progressive visual impairment. These findings suggest that, while circadian sleep-wake rhythm remain intact, patients with Usher syndrome type 2a suffer from sleep disturbances that likely arise from factors beyond their progressive blindness. With sleep problems being a major risk factor for physical and mental health problems, we advocate that sleep problems should be recognized as a hallmark symptom of Usher syndrome type 2a, warranting in-depth research for potential targeted therapeutic interventions.
本研究旨在增进我们对睡眠问题作为2a型Usher综合征所致遗传性聋盲合并症的理解。15例经基因诊断确诊的2a型Usher综合征患者和15名未受影响的对照者参与了为期2周的综合睡眠和活动评估,使用MotionWatch 8活动记录仪和统一睡眠日记。分析了包括睡眠机会窗口、入睡潜伏期、睡眠效率和自我报告的睡眠质量在内的各种睡眠参数。进行了非参数昼夜节律分析以评估昼夜节律性。此外,还进行了回归分析,以研究睡眠参数与患者人口统计学和疾病进展之间的潜在相关性。与对照组相比,2a型Usher综合征患者的入睡潜伏期明显更长,自我报告的睡眠和休息质量更低。此外,患者群体中睡眠效率和入睡潜伏期的每日变异性明显更高。非参数昼夜节律分析显示昼夜节律性无显著差异。回归分析表明,患有2a型Usher综合征是睡眠结果不佳的一个重要预测因素。未发现视力损害程度与睡眠参数之间存在明显相关性,这表明2a型Usher综合征对睡眠的负面影响独立于进行性视力损害而表现出来。这些发现表明,虽然昼夜睡眠-觉醒节律保持完整,但2a型Usher综合征患者存在睡眠障碍,这些障碍可能源于其进行性失明以外的因素。由于睡眠问题是身心健康问题的主要危险因素,我们主张应将睡眠问题视为2a型Usher综合征的标志性症状,值得对潜在的靶向治疗干预措施进行深入研究。