Clinical Characterization and Long-Term Outcome in Children and Adults With Anti-AMPA Receptor Encephalitis.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Chiara Milano, Ezgi Saylam, Claudia Papi, Laura Marmolejo, Alexandra Sankovic, Raphael Reinecke, Jeroen Kerstens, Chiara Pizzanelli, Mateus Mistieri Simabukuro, Marie Benaiteau, Bastien Joubert, Matteo Gastaldi, Lívia Almeida Dutra, Frank Leypoldt, Mareike Jansen, Izumi Kawachi, Hisanao Akiyama, Nikolas Boy, Silvia Bozzetti, Peter Broegger Christensen, Pietro Businaro, Alessandro Dinoto, Tal Friedman-Korn, Urara Fujiwara, Tatsuya Fukumoto, Kenshiro Fuse, Sam Ishmael Hooshmand, Lauren Hurst, Raffaele Iorio, Isabelle Korn-Lubetzki, André Filipe Lucchi Rodrigues, Sara Mariotto, Johannes Michael, Yuko Morimoto, Rinze Frederik Neuteboom, Amanda L Piquet, Andrea O Rossetti, Sabine Rumpler-Kreiner, Jonathan D Santoro, Florian Schwendinger, Brenda Shen, Steffen Syrbe, Johannes Troger, Ingrid Wagner, Christian G Bien, Eugenia Martinez-Hernandez, Thais Armangue, Romana Höftberger, Takahiro Iizuka, Maarten J Titulaer, Jerome Honnorat, Francesc Graus, Josep O Dalmau, Setty Magaña, Marianna Spatola
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引用次数: 0

Abstract

Background and objectives: Anti-alpha-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor (anti-AMPAR) encephalitis manifests as limbic encephalitis in adults and is often associated with cancer. Although some reports suggest that it may occur in children, the clinical features in this population, as well as the prognostic factors and long-term outcomes in children and adults, are unknown.

Methods: We performed a retrospective, international collaborative study of patients with anti-AMPAR encephalitis. Clinical information was reviewed, together with data from published pediatric patients. Clinical features of children and adults were compared with nonparametric tests. Survival rates (Kaplan-Meier curves) were compared using log-rank tests. Prognostic factors of poor outcome (modified Rankin Scale score >2) were identified using logistic regression models.

Results: A total of 115 patients were included, of whom 84 (71 adults, 13 children) had only AMPAR antibodies and 31 (27 adults, 4 children) had additional concurrent neural antibodies. Among patients with AMPAR antibodies alone, tumors were identified in 37 adults (56%) and none of the children (p < 0.0001). Children were more likely than adults to have behavioral/psychiatric symptoms (5/13, 39%, vs 8/71, 11%, p = 0.026) at onset, cerebellar dysfunction (6/13, 46%, vs 7/68, 10% p = 0.005) or movement disorders (5/13, 39%, vs 8/67, 12%, p = 0.032) during the disease course, and extratemporal brain MRI lesions (4/9, 44%, vs 5/44, 11%, p = 0.035). Among 34 patients with prolonged follow-up (>24 months), long-term neurocognitive sequelae were reported in 23 (68%), all adults. Failure to respond to first-line immunotherapy at multivariable analysis predicted a poor outcome (OR 8.0, 95% CI 1.1-59.2, p = 0.043). Among the 31 patients with concurrent neural autoantibodies, 22 (79%) had a tumor; those with high-risk antibodies had lower survival rates (p = 0.008).

Discussion: Children and adults with anti-AMPAR encephalitis show distinct clinical-radiologic features. At long-term follow-up, 68% of patients, all adults, have neurologic sequelae, with failure to respond to first-line immunotherapy being associated with worse outcomes.

儿童和成人抗ampa受体脑炎的临床特征和长期预后。
背景和目的:抗α -氨基-3-羟基-5-甲基-4-异恶唑-丙酸受体(anti-AMPAR)脑炎在成人中表现为边缘脑炎,通常与癌症相关。虽然一些报告表明它可能发生在儿童身上,但这一人群的临床特征,以及儿童和成人的预后因素和长期结果尚不清楚。方法:我们对抗ampar脑炎患者进行了回顾性的国际合作研究。我们回顾了临床资料,以及来自已发表的儿科患者的数据。采用非参数检验对儿童和成人的临床特征进行比较。生存率(Kaplan-Meier曲线)采用对数秩检验进行比较。采用logistic回归模型确定不良预后因素(改良Rankin量表评分>2)。结果:共纳入115例患者,其中84例(71例成人,13例儿童)仅携带AMPAR抗体,31例(27例成人,4例儿童)同时携带神经抗体。在单独携带AMPAR抗体的患者中,37名成人(56%)发现肿瘤,没有儿童(p < 0.0001)。儿童在发病时比成人更容易出现行为/精神症状(5/13,39%,对8/71,11%,p = 0.026),在病程中更容易出现小脑功能障碍(6/13,46%,对7/68,10% p = 0.005)或运动障碍(5/13,39%,对8/67,12%,p = 0.032),以及颞外脑MRI病变(4/9,44%,对5/44,11%,p = 0.035)。在34例延长随访(bbb - 24个月)的患者中,有23例(68%)报告了长期神经认知后遗症,均为成年人。在多变量分析中,对一线免疫治疗反应不佳的患者预后较差(OR 8.0, 95% CI 1.1-59.2, p = 0.043)。在并发神经自身抗体的31例患者中,22例(79%)有肿瘤;携带高危抗体的患者生存率较低(p = 0.008)。讨论:儿童和成人抗ampar脑炎表现出不同的临床-放射学特征。在长期随访中,68%的成人患者有神经系统后遗症,对一线免疫治疗无效的患者预后较差。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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