Cognitive deficits following anti-NMDA receptor encephalitis

BackgroundAnti-NMDA receptor (NMDAR) encephalitis is a recently characterised autoimmune disorder mainly affecting young women. Although the clinical features of the acute disease are well characterised, cognitive long-term outcome has not been examined in detail.MethodsThe authors investigated cogn...

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Published inJournal of neurology, neurosurgery and psychiatry Vol. 83; no. 2; pp. 195 - 198
Main Authors Finke, Carsten, Kopp, Ute A, Prüss, Harald, Dalmau, Josep, Wandinger, Klaus-Peter, Ploner, Christoph J
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd 01.02.2012
BMJ Publishing Group
BMJ Publishing Group LTD
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Summary:BackgroundAnti-NMDA receptor (NMDAR) encephalitis is a recently characterised autoimmune disorder mainly affecting young women. Although the clinical features of the acute disease are well characterised, cognitive long-term outcome has not been examined in detail.MethodsThe authors investigated cognitive performance in nine patients with proven anti-NMDAR encephalitis after recovery from the acute disease period (median 43 months after disease onset, range 23 to 69). Patients underwent a comprehensive neuropsychological assessment, including memory tasks that have previously been shown to be sensitive for hippocampal dysfunction.ResultsSubstantial persistent cognitive impairments were observed in eight out of nine patients that mainly consisted of deficits in executive functions and memory. The severity of these deficits varied inter-individually. Patients with early immunotherapy performed significantly better. The most severe deficits were observed with inefficient or delayed initial treatment.ConclusionOur results suggest that cognitive deficits constitute a major long-term morbidity of anti-NMDAR encephalitis. These deficits relate to the distribution of NMDARs in the human brain and their functional role in normal cognition. Good cognitive long-term outcome may depend on early and aggressive treatment.
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PMID:21933952
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ArticleID:jnnp-2011-300411
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ISSN:0022-3050
1468-330X
DOI:10.1136/jnnp-2011-300411