Cardiovascular autonomic dysfunction and sleep abnormalities in children with Prader-Willi syndrome.

IF 3.9 3区 医学 Q1 CLINICAL NEUROLOGY
Rachel Debs, Gwenaëlle Diene, Julie Cortadellas, Catherine Molinas, Marc Kermorgant, Maïthé Tauber, Anne Pavy Le Traon
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Abstract

Purpose: Prader-Willi syndrome (PWS) is a rare genetic neurodevelopmental condition characterized by cognitive disabilities, behavioral problems, hypothalamic dysfunction with obesity, and sleep disorders. A few studies have reported autonomic nervous system dysfunction. Our aim was to investigate dysautonomia by combining sleep studies and standard autonomic testing in regularly followed children with PWS.

Methods: In this retrospective study, heart rate variability was analyzed during each sleep stage (polysomnography) using time and frequency domains in PWS children (N = 37) compared with age-matched controls (N = 20). Cardiovascular autonomic testing (Ewing tests) and sweating assessment (electrochemical skin conductance) were also performed in patients over 6 years (N = 23).

Results: Autonomic testing: Heart rate changes with active standing and with deep breathing were impaired in 47% and 22% of the children, respectively. Asymptomatic orthostatic hypotension (OH) was found in 26%. Baroreflex sensitivity in supine position was in normal range (14.1 ± 6.7 ms/mmHg). Electrochemical skin conductance was normal. Sleep study: 46% of the children with PWS had obstructive sleep apnea and 24% had central sleep apnea. None of these events were observed in the control group. Mean R-R and time domain heart rate variability parameters were significantly lower compared with controls in N2 and Rapid Eye Movement (REM) sleep stages. Narcoleptic-like phenotype was found in 47% associated with lower low-frequency (LF) power (sympathetic index) in REM sleep.

Conclusion: Our study confirms a decreased vagal modulation during both wakefulness and sleep in children with PWS. OH in some patients suggests a sympathetic dysfunction. These changes may contribute to the increased cardiovascular risk in PWS.

Prader-Willi综合征患儿的心血管自主神经功能障碍和睡眠异常。
目的:Prader-Willi综合征(PWS)是一种罕见的遗传性神经发育疾病,以认知障碍、行为问题、下丘脑功能障碍伴肥胖和睡眠障碍为特征。少数研究报告了自主神经系统功能障碍。我们的目的是通过结合睡眠研究和定期随访的PWS儿童的标准自主神经测试来研究自主神经障碍。方法:在这项回顾性研究中,使用时间和频率域分析PWS儿童(N = 37)与年龄匹配的对照组(N = 20)在每个睡眠阶段的心率变异性(多导睡眠图)。6岁以上的患者(N = 23)也进行了心血管自主测试(Ewing试验)和出汗评估(皮肤电导电化学)。结果:自主神经测试:47%和22%的儿童在主动站立和深呼吸时心率变化受损。无症状体位性低血压(OH)占26%。仰卧位压反射敏感性正常(14.1±6.7 ms/mmHg)。皮肤电导正常。睡眠研究:46%的PWS患儿患有阻塞性睡眠呼吸暂停,24%患有中枢性睡眠呼吸暂停。在对照组中没有观察到这些事件。N2和快速眼动(REM)睡眠阶段的平均R-R和时域心率变异性参数显著低于对照组。发作性睡样表型与REM睡眠中较低的低频(LF)功率(交感神经指数)相关的比例为47%。结论:我们的研究证实了PWS患儿清醒和睡眠时迷走神经调节的减少。部分患者的OH提示交感神经功能障碍。这些变化可能导致PWS患者心血管风险增加。
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来源期刊
Clinical Autonomic Research
Clinical Autonomic Research 医学-临床神经学
CiteScore
7.40
自引率
6.90%
发文量
65
审稿时长
>12 weeks
期刊介绍: Clinical Autonomic Research aims to draw together and disseminate research work from various disciplines and specialties dealing with clinical problems resulting from autonomic dysfunction. Areas to be covered include: cardiovascular system, neurology, diabetes, endocrinology, urology, pain disorders, ophthalmology, gastroenterology, toxicology and clinical pharmacology, skin infectious diseases, renal disease. This journal is an essential source of new information for everyone working in areas involving the autonomic nervous system. A major feature of Clinical Autonomic Research is its speed of publication coupled with the highest refereeing standards.
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