Division of Cardiology, Department of Medicine, Columbia University Medical Center, Columbia University, 630 W 168th Street, New York, NY 10032, USA.
Europace. 2012 Aug;14(8):1188-94. doi: 10.1093/europace/eus014. Epub 2012 Feb 15.
Anti-N-methyl-D-aspartate receptor encephalitis (NMDARE) is a recently recognized form of autoimmune encephalitis that typically affects young women, often as a paraneoplastic syndrome related to ovarian teratoma. Clinical features include psychiatric and neurological disturbances, central hypoventilation, autonomic instability, and cardiac dysrhythmias. The prevalence, nature, and outcomes of cardiac dysrhythmias in patients with NMDARE have not been well described.
Records of 10 consecutive patients with NMDARE were reviewed to obtain clinical, laboratory, echocardiographic, electrocardiographic, and radiological data. Patients were all female with an average age of 23 ± 5.5 years. Echocardiograms revealed structurally normal hearts with the exception of mild left ventricular hypertrophy in two cases. Eight patients had inappropriate sinus tachycardia. Six patients developed significant sinus bradycardia, which included periods of sinus arrest in four cases. Five patients manifested both sinus bradycardia and tachycardia. Bradycardia was often triggered by identifiable vagal stimuli. Temporary pacing was instituted in three patients, but permanent pacing was not required in any of the patients. Magnetic resonance imaging (MRI) scans revealed mesial temporal abnormalities in nine patients. In all cases, the dysrhythmias resolved with treatment of the underlying immune disorder with immunotherapy and/or teratoma resection. There was no evidence of dysrhythmia recurrence in any patient at follow-up.
Anti-N-methyl-D-aspartate receptor encephalitis is a recently recognized cause of autoimmune encephalitis with a predilection to cause severe sinus node abnormalities. Temporary pacing is occasionally required, but permanent pacing appears to be unnecessary. An analysis of the clinical syndrome coupled with MRI and experimental data may offer insight into central mechanisms of heart rate regulation.
抗 N-甲基-D-天冬氨酸受体脑炎(NMDARE)是一种最近被认识到的自身免疫性脑炎形式,通常影响年轻女性,常作为与卵巢畸胎瘤相关的副肿瘤综合征。临床特征包括精神和神经紊乱、中枢性通气不足、自主神经不稳定和心律失常。NMDARE 患者心律失常的患病率、性质和结局尚未得到很好的描述。
回顾了 10 例连续 NMDARE 患者的记录,以获取临床、实验室、超声心动图、心电图和影像学数据。患者均为女性,平均年龄 23±5.5 岁。超声心动图显示除 2 例存在轻度左心室肥厚外,心脏结构正常。8 例患者出现不适当窦性心动过速。6 例患者出现明显窦性心动过缓,其中 4 例出现窦性停搏。5 例患者同时出现窦性心动过缓和心动过速。心动过缓常由可识别的迷走神经刺激触发。3 例患者进行了临时起搏,但所有患者均未进行永久性起搏。磁共振成像(MRI)扫描显示 9 例患者存在内侧颞叶异常。在所有情况下,心律失常均随着免疫治疗和/或畸胎瘤切除治疗潜在免疫性疾病而得到缓解。在随访中,没有任何患者出现心律失常复发的证据。
抗 N-甲基-D-天冬氨酸受体脑炎是一种最近被认识到的自身免疫性脑炎的病因,易引起严重的窦房结异常。偶尔需要临时起搏,但永久性起搏似乎是不必要的。对临床综合征的分析结合 MRI 和实验数据,可能有助于深入了解心率调节的中枢机制。