Ferri Raffaele, Miano Silvia, Bruni Oliviero, Vankova Jitka, Nevsimalova Sona, Vandi Stefano, Montagna Pasquale, Ferini-Strambi Luigi, Plazzi Giuseppe
Department of Neurology IC, Sleep Research Centre, Oasi Institute (IRCCS), Troina, Enna, Italy.
Clin Neurophysiol. 2005 Nov;116(11):2675-84. doi: 10.1016/j.clinph.2005.08.004. Epub 2005 Oct 10.
NREM sleep patterns of narcoleptic patients with cataplexy were studied, focusing on their sleep 'microstructure', by analyzing the cyclic alternating pattern (CAP).
Forty-nine HLA DQB1*0602-positive patients with narcolepsy/cataplexy (32 men and 17 women, aged 18-46 years) were included together with 37 age-matched normal controls. Each subject underwent one polysomnographic night recording after an adaptation night. Sleep stages were scored following standard criteria and CAP A phases were detected and classified into 3 subtypes (A1, A2, and A3). Power spectra for frequencies between 0.5 and 25 Hz were obtained for each CAP condition, separately in sleep stage 2 and SWS.
Narcoleptic patients displayed reduced total CAP rate. A selective reduction in the number of A1 subtypes/hour and a reduced A3 index were found in narcoleptics who had also a smaller average number of CAP sequences. Narcoleptic patients had higher power spectra for fast frequencies mostly during SWS, while REM sleep power spectra showed significantly higher power density for frequency bins 0.5-1.5, 8.5-9.5, and 17.5-25 Hz. Similarly, CAP A1 subtypes and NCAP epochs during SWS displayed significantly higher power density for fast frequency bins.
The main finding of this study is that the occurrence of the A1 CAP subtypes is impaired during NREM sleep in narcoleptic patients. Thus, narcolepsy seems to be accompanied not only by alterations of REM but also NREM sleep which is subtly but significantly impaired, as reflected by CAP and the corresponding EEG spectral analysis.
Our findings might indicate that in narcolepsy very-slow oscillation processes less effective than normal might be present, with a subtly impaired capability of grouping the other sleep EEG activities; this aspect deserves further insight in order to obtain a better understanding of its functional meaning.
通过分析周期性交替模式(CAP),研究发作性睡病伴猝倒患者的非快速眼动(NREM)睡眠模式,重点关注其睡眠“微观结构”。
纳入49例 HLA DQB1*0602 阳性的发作性睡病/猝倒患者(32例男性和17例女性,年龄18 - 46岁)以及37例年龄匹配的正常对照。每位受试者在适应一晚后进行一晚的多导睡眠图记录。按照标准标准对睡眠阶段进行评分,并检测CAP A期并分为3种亚型(A1、A2和A3)。分别在睡眠2期和慢波睡眠(SWS)中,针对每种CAP情况获取0.5至25Hz频率之间的功率谱。
发作性睡病患者的总CAP率降低。在平均CAP序列数也较少的发作性睡病患者中,发现每小时A1亚型数量选择性减少以及A3指数降低。发作性睡病患者大多在SWS期间快速频率的功率谱较高,而快速眼动(REM)睡眠功率谱在0.5 - 1.5、8.5 - 9.5和17.5 - 25Hz频段显示出明显更高的功率密度。同样,SWS期间的CAP A1亚型和非CAP(NCAP)时段在快速频率频段显示出明显更高的功率密度。
本研究的主要发现是发作性睡病患者在NREM睡眠期间A1 CAP亚型的出现受损。因此,发作性睡病似乎不仅伴有REM睡眠改变,而且NREM睡眠也受到细微但显著的损害,如CAP及相应脑电图频谱分析所反映的那样。
我们的发现可能表明,在发作性睡病中可能存在比正常情况效率更低的极慢振荡过程,将其他睡眠脑电图活动分组的能力受到细微损害;这方面值得进一步深入研究,以便更好地理解其功能意义。