Child Neurology and Clinical Neurophysiology, Pediatric University Hospital, via Giustiniani n.3, Padua, Italy.
Department of Medical Sciences, Pediatric Section, University of Ferrara, Italy.
Arch Clin Neuropsychol. 2019 Nov 27;34(8):1309-1319. doi: 10.1093/arclin/acy088.
Anti-N-methyl-d-aspartate receptor (NMDAR) encephalitis is a severe, but treatable, autoimmune disorder, characterized by autoantibodies causing hypofunction of blocking NMDA receptors leading to a unique constellation of cognitive, motor, and psychiatric symptoms. Neuropsychological and psychopathological outcome has not been fully explored, particularly in children. Aim of this study was to investigate pediatric anti-NMDAR encephalitis as a model of impairment of the complex frontal-subcortical circuits who are implicated in several of the childhood neuropsychiatric disorders.
Seven children diagnosed with anti-NMDAR encephalitis at our department underwent an evaluation of the global mental functioning before discharge, a neuropsychological and psychological/behavioral standardized examination within one month after discharge and subsequently were followed up longitudinally for mean 35 months (range 24-48 months). Collected neuropsychological data were evaluated retrospectively.
Deficits in attention, executive functions and/or visual motor functions involving executive functions were seen in all children within one month after discharge. These deficits were long lasting in about a half of the patients. In addition, four patients developed persistent psychopathological dysfunctions: difficulties to regulate their own behavior, impulsivity, hyperactivity, irritability, apathy, and obsessive-compulsive symptoms.
Our data are in line with research suggesting a crucial role of the executive functions impairments in cognitive outcome disturbance of anti-NMDAR encephalitis. We found also behavioral and psychological deficits pointing to a more comprehensive framework of frontal-subcortical dysfunction, in which the NMDA mediated transmission appear to have a role, as suggested by neurobiological, pharmacological, and neuroimaging studies.
抗 N-甲基-D-天冬氨酸受体(NMDAR)脑炎是一种严重但可治疗的自身免疫性疾病,其特征是自身抗体导致 NMDA 受体功能障碍,从而引起认知、运动和精神症状的独特组合。神经心理学和精神病理学结果尚未得到充分探讨,尤其是在儿童中。本研究旨在探讨儿科抗 NMDAR 脑炎作为涉及多种儿童神经精神障碍的复杂额皮质下回路损伤的模型。
我们科室诊断出的 7 名抗 NMDAR 脑炎患儿在出院前接受了全面的精神功能评估,在出院后 1 个月内接受了神经心理学和心理/行为标准化检查,随后进行了平均 35 个月(24-48 个月)的纵向随访。回顾性评估收集的神经心理学数据。
所有患儿在出院后 1 个月内均出现注意力、执行功能和/或涉及执行功能的视觉运动功能缺陷。大约一半的患儿存在长期缺陷。此外,4 名患者出现持续的精神病理学功能障碍:难以控制自己的行为、冲动、多动、易怒、冷漠和强迫症状。
我们的数据与研究结果一致,表明执行功能障碍在抗 NMDAR 脑炎认知结果障碍中起着关键作用。我们还发现了行为和心理缺陷,表明额皮质下功能障碍的更全面框架,其中 NMDA 介导的传递似乎起作用,这得到了神经生物学、药理学和神经影像学研究的支持。