Not Only Sleepwalking But NREM Parasomnia Irrespective of the Type Is Associated with HLA DQB1*05:01

被引:43
作者
Heidbreder, Anna [1 ,2 ]
Frauscher, Birgit [2 ]
Mitterling, Thomas [2 ]
Boentert, Matthias [1 ]
Schirmacher, Anja [1 ]
Hoertnagl, Paul [7 ]
Schennach, Harald [7 ]
Massoth, Christina [1 ]
Happe, Svenja [3 ,4 ]
Mayer, Geert [5 ,6 ]
Young, Peter [1 ]
Hoegl, Birgit [2 ]
机构
[1] Univ Hosp Muenster, Dept Sleep Med & Neuromuscular Disorders, Munster, Germany
[2] Med Univ Innsbruck, Dept Neurol, Anichstr 35, AU-6020 Innsbruck, Austria
[3] Clin Maria Frieden Telgte, Dept Neurol, Telgte, Germany
[4] Univ Gottingen, D-37073 Gottingen, Germany
[5] Hephata Klin Schwalmstadt Treysa, Schwalmstadt, Germany
[6] Univ Marburg, Dept Neurol, Marburg, Germany
[7] Med Univ Innsbruck, Cent Inst Blood Transfus & Immunol, A-6020 Innsbruck, Austria
来源
JOURNAL OF CLINICAL SLEEP MEDICINE | 2016年 / 12卷 / 04期
关键词
video-polysomnography; genotype; somnambulism; genetics; behavior; FRONTAL-LOBE EPILEPSY; ADULT SLEEPWALKERS; GENERAL-POPULATION; SLEEP-DEPRIVATION; NIGHT-TERRORS; SOMNAMBULISM; NARCOLEPSY; GENETICS; AROUSALS; PREVALENCE;
D O I
10.5664/jcsm.5692
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: Despite the high prevalence and clinical relevance of NREM parasomnias, data on supportive genetic markers are scarce, and mainly refer to sleepwalking only. Methods: We retrospectively analyzed clinical, polysomnographic, and HLA findings of 74 adults (37 men) with NREM parasomnia gathered from four neurological sleep centers. Parasomniac events were classified according to ICSD-2 criteria. HLA DQB1 genotyping was compared to regional-matched reference allele-frequencies. Results: Fifty-six patients had more than 2 different parasomnia type: 11 sleepwalking, 4 sleep terrors, 3 confusional arousals only. Parasomniac events were documented during video-polysomnography (V-PSG) in 70% (49/70) of subjects (71.4% confusional arousals, 8.2% sleep terrors, 4.1% sleepwalking, 16.3% >= 2 NREM parasomnia types). Violent behavior during V-PSG occurred in 8.5% (6/71). NREM parasomnia onset was reported after the age of 30 years in 6.8% (5/74). The HLA DQB1*05:01 allele was present in 41% (29/71) compared to 24.2% in the regional-matched reference allele group (p < 0.05). This haplotype prevalence did not differ within the NREM parasomnia type. Epworth Sleepiness Score was 10 or higher in 28.6%. Conclusions: This is a large polysomnography-based case series of patients with NREM parasomnia. In patients with suspected sleepwalking or sleep terrors, polysomnography is highly useful in detecting arousals from NREM sleep as a marker of NREM parasomnia. We confirmed previous findings by demonstrating a high prevalence of the HLA DQB1*05:01 genotype for different types of NREM parasomnias. Our findings therefore support a common genetic background, and corroborate the importance of video-polysomnography in the work-up of parasomnia.
引用
收藏
页码:565 / 570
页数:6
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