Steiner Oliver L, Angela Claudia, Klostermann Fabian
Department of Neurology, Motor and Cognition Group, Charité-Universitätsmedizin Berlin, Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
Berlin School of Mind and Brain, Humboldt-Universität zu Berlin, Berlin, Germany.
Eur J Neurol. 2025 Nov;32(11):e70408. doi: 10.1111/ene.70408.
Chronic inflammatory demyelinating polyneuropathy (CIDP) is a dysimmune disease leading to sensorimotor deficits due to peripheral nerve dysfunction, but recently additional non-sensorimotor symptoms (NSMS) were increasingly recognized. In this context, we compared the sleep behavior in persons with versus without CIDP and discussed the results with respect to further NSMS.
Twenty-five CIDP patients and 27 controls took part in this prospective, cross-sectional study. Clinically, sensorimotor disability (RODS), affective state (DESC-I), and fatigue levels (FSMC scores) were assessed. Regarding sleep-wake behavior, they wore actigraphic devices over 14 consecutive days and completed sleep diaries, chronotype questionnaires, and the Pittsburgh Sleep Quality Index (PSQI). The actigraphic data were analyzed with respect to sleep efficiency, wake after sleep onset (WASO), sleep onset latency, total sleep duration, intradaily variability (IV), and interdaily stability (IS).
Patients with CIDP reported significantly worse subjective sleep quality (p < 0.001). They also showed higher levels of fatigue (p < 0.001) and depressiveness (p = 0.046). The actigraphic results showed significantly reduced WASO (p = 0.012), especially early in the morning and immediately preceding waking up (p = 0.010). The sleep abnormalities were not linked to the raised clinical data (p > 0.05).
Beyond subjectively reduced sleep quality, actigraphic data show that persons with CIDP have lowered sleep efficacy and experience increased nocturnal arousals. This suggests that sleep disturbance is a genuine aspect of CIDP adding to the underrecognized problem of NSMS in this condition.
慢性炎性脱髓鞘性多发性神经病(CIDP)是一种免疫功能异常疾病,因周围神经功能障碍导致感觉运动功能缺损,但最近人们越来越多地认识到其存在额外的非感觉运动症状(NSMS)。在此背景下,我们比较了患有和未患有CIDP的人群的睡眠行为,并结合进一步的NSMS讨论了结果。
25例CIDP患者和27名对照者参与了这项前瞻性横断面研究。临床上,评估了感觉运动功能障碍(RODS)、情感状态(DESC-I)和疲劳水平(FSMC评分)。关于睡眠-觉醒行为,他们连续14天佩戴活动记录仪,并完成睡眠日记、昼夜节律问卷和匹兹堡睡眠质量指数(PSQI)。对活动记录仪数据进行了睡眠效率、睡眠后觉醒(WASO)、入睡潜伏期、总睡眠时间、日内变异性(IV)和日间稳定性(IS)方面的分析。
CIDP患者报告的主观睡眠质量明显更差(p < 0.001)。他们还表现出更高水平的疲劳(p < 0.001)和抑郁(p = 0.046)。活动记录仪结果显示WASO显著降低(p = 0.012),尤其是在清晨和即将醒来之前(p = 0.010)。睡眠异常与升高的临床数据无关(p > 0.05)。
除了主观上睡眠质量下降外,活动记录仪数据显示,CIDP患者的睡眠效率降低,夜间觉醒增加。这表明睡眠障碍是CIDP的一个真实方面,加重了这种情况下未被充分认识的NSMS问题。