PMID- 30418503 OWN - NLM STAT- MEDLINE DCOM- 20200311 LR - 20200311 IS - 1873-5843 (Electronic) IS - 0887-6177 (Linking) VI - 34 IP - 8 DP - 2019 Nov 27 TI - Neuropsychological And Psychopathological Profile Of Anti-Nmdar Encephalitis: A Possible Pathophysiological Model For Pediatric Neuropsychiatric Disorders. PG - 1309-1319 LID - 10.1093/arclin/acy088 [doi] AB - OBJECTIVE: 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. METHOD: 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. RESULTS: 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. CONCLUSIONS: 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. CI - (c) The Author(s) 2018. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com. FAU - Cainelli, Elisa AU - Cainelli E AD - Child Neurology and Clinical Neurophysiology, Pediatric University Hospital, via Giustiniani n.3, Padua, Italy. FAU - Nosadini, Margherita AU - Nosadini M AD - Child Neurology and Clinical Neurophysiology, Pediatric University Hospital, via Giustiniani n.3, Padua, Italy. FAU - Sartori, Stefano AU - Sartori S AD - Child Neurology and Clinical Neurophysiology, Pediatric University Hospital, via Giustiniani n.3, Padua, Italy. FAU - Suppiej, Agnese AU - Suppiej A AD - Child Neurology and Clinical Neurophysiology, Pediatric University Hospital, via Giustiniani n.3, Padua, Italy. AD - Department of Medical Sciences, Pediatric Section, University of Ferrara, Italy. LA - eng PT - Journal Article PL - United States TA - Arch Clin Neuropsychol JT - Archives of clinical neuropsychology : the official journal of the National Academy of Neuropsychologists JID - 9004255 SB - IM MH - Adolescent MH - Anti-N-Methyl-D-Aspartate Receptor Encephalitis/*physiopathology/*psychology MH - Attention Deficit Disorder with Hyperactivity/etiology/psychology MH - Child MH - Child Behavior MH - Child Behavior Disorders/etiology/physiopathology/psychology MH - Child, Preschool MH - Executive Function MH - Female MH - Follow-Up Studies MH - Frontal Lobe/physiopathology MH - Humans MH - Longitudinal Studies MH - Male MH - Mental Disorders/etiology/*physiopathology/*psychology MH - Mental Processes MH - Nervous System Diseases/etiology/*physiopathology/*psychology MH - Neuropsychological Tests MH - Retrospective Studies OTO - NOTNLM OT - Behavioral OT - Executive functions OT - Frontal-subcortical circuits, NMDAR encephalitis OT - Psychological EDAT- 2018/11/13 06:00 MHDA- 2020/03/12 06:00 CRDT- 2018/11/13 06:00 PHST- 2018/05/16 00:00 [received] PHST- 2018/08/30 00:00 [revised] PHST- 2018/10/18 00:00 [accepted] PHST- 2018/11/13 06:00 [pubmed] PHST- 2020/03/12 06:00 [medline] PHST- 2018/11/13 06:00 [entrez] AID - 5173740 [pii] AID - 10.1093/arclin/acy088 [doi] PST - ppublish SO - Arch Clin Neuropsychol. 2019 Nov 27;34(8):1309-1319. doi: 10.1093/arclin/acy088.