Silber Michael H
Center for Sleep Medicine and Department of Neurology, Mayo Clinic College of Medicine, Rochester, MN, USA.
Handb Clin Neurol. 2016;133:317-26. doi: 10.1016/B978-0-444-63432-0.00018-9.
A number of autoantibodies, some paraneoplastic, are associated with sleep disorders. Morvan syndrome and limbic encephalitis, associated with voltage-gated potassium channel-complex antibodies, principally against CASPR2 and LGI1, can result in profound insomnia and rapid eye movement sleep behavior disorder (RBD). Patients with aquaporin-4 antibodies and neuromyelitis optica may develop narcolepsy in association with other evidence of hypothalamic dysfunction, sometimes as the initial presentation. Central sleep apnea and central neurogenic hypoventilation are found in patients with anti-N-methyl-d-aspartate receptor antibody encephalitis, and obstructive sleep apnea, stridor, and hypoventilation are prominent features of a novel tauopathy associated with IgLON5 antibodies. In addition, paraneoplastic diseases may involve the hypothalamus and cause sleep disorders, particularly narcolepsy and RBD in those with Ma1 and Ma2 antibodies. Patients with antineuronal nuclear autoantibodies type 2 may develop stridor. Several lines of evidence suggest that narcolepsy is an autoimmune disorder. There is a strong relationship with the human leukocyte antigen (HLA) DQB1*06:02 haplotype and polymorphisms in the T-cell receptor alpha locus and purinergic receptor P2Y11 genes. Patients with recent-onset narcolepsy may have high titers of antistreptococcal or other antibodies, although none has yet been shown to be disease-specific but, supporting an immune basis, recent evidence indicates that narcolepsy in children can be precipitated by one type of vaccination against the 2009-2010 H1N1 influenza pandemic.
许多自身抗体,有些是副肿瘤性的,与睡眠障碍有关。莫旺综合征和边缘性脑炎与电压门控钾通道复合物抗体有关,主要针对接触蛋白相关蛋白2(CASPR2)和富含亮氨酸胶质瘤失活蛋白1(LGI1),可导致严重失眠和快速眼动睡眠行为障碍(RBD)。水通道蛋白4抗体阳性的视神经脊髓炎患者可能会出现发作性睡病,并伴有下丘脑功能障碍的其他证据,有时发作性睡病是首发表现。抗N-甲基-D-天冬氨酸受体抗体脑炎患者会出现中枢性睡眠呼吸暂停和中枢性神经源性通气不足,而与IgLON5抗体相关的一种新型tau蛋白病的突出特征是阻塞性睡眠呼吸暂停、喘鸣和通气不足。此外,副肿瘤性疾病可能累及下丘脑并导致睡眠障碍,特别是在有Ma1和Ma2抗体的患者中出现发作性睡病和RBD。2型抗神经元细胞核自身抗体阳性的患者可能会出现喘鸣。有几条证据表明发作性睡病是一种自身免疫性疾病。它与人类白细胞抗原(HLA)DQB1*06:02单倍型以及T细胞受体α基因座和嘌呤能受体P2Y11基因的多态性有很强的关联。近期发病的发作性睡病患者可能有高滴度的抗链球菌或其他抗体,尽管尚未证明其中任何一种抗体具有疾病特异性,但近期证据表明,针对2009 - 2010年甲型H1N1流感大流行的一种疫苗接种可能会引发儿童发作性睡病,这支持了其免疫基础。