作者
Mar Guasp,Mireia Rosa-Justícia,Amaia Muñoz‐Lopetegi,Eugenia Martínez‐Hernández,Thaís Armangué,Gisela Sugranyes,Heike Stein,R. Borras,Laia Prades,Helena Ariño,Jesús Planagumà,Elena De-La-Serna,Domingo Escudero,Sara Llufriú,Raquel Sánchez‐Valle,Joan Santamaría,Albert Compte,Josefina Castro‐Fornieles,Josep Dalmau,Dolores Páramo,Vicente Abril López de Medrano,V. Casado,Nicolau Guanyabens,Eloi Giné-Servén,María Ángeles del Real,J. R. Pardo,Leticia Martin-Gil,Francisco Javier Barrero,Nuria García‐Barragán,Mercè Falip,Marta Simó,E. Rodrı́guez,Juan José Ruiz Ezquerro,Luís Bataller,Gemma Safont,José Vicente-Hervàs,Luís Brieva,Ignacio Casado,Juan Carlos Portilla-Cuenca,Sònia Escalante,Juan F. Arenillas,Elena Erro,Ivonne Jericó-Pascual,Alejandro Fuerte‐Hortigón,Alba Morató,Albert Saiz,Yolanda Blanco,María Sepúlveda,Raquel Ruiz‐García,Laura Naranjo,Maria Rodés,Esther Aguilar,Mercè Alba,Eva Caballero
摘要
Anti-NMDA receptor (NMDAR) encephalitis is associated with a post-acute stage that is not well known. We aimed to describe the clinical features of this stage, similarities with schizophrenia spectrum disorders, and the factors that predict cognitive-psychiatric outcomes and could serve as prognostic biomarkers.In this prospective cohort study, participants (aged 12-60 years) with anti-NMDAR encephalitis during the post-acute stage visited Hospital Clínic de Barcelona (Barcelona, Spain) on three occasions (at study entry [V1], at 6 months [V2], and at 12 months [V3]) and underwent comprehensive neuropsychiatric evaluations. Similar evaluations were done in a group of age-matched participants with schizophrenia spectrum disorders and a group of age-matched and sex-matched healthy participants also recruited from Hospital Clínic de Barcelona. We analysed differences between and within groups in the longitudinal follow-up using multilevel linear mixed-effect models, adjusting for group, age, sex, and socioeconomic status to control for possible confounding.Between Jan 1, 2017, and Sept 30, 2020, 82 participants were recruited, 28 (34%) with anti-NMDAR encephalitis, 27 (33%) with schizophrenia spectrum disorders, and 27 (33%) healthy participants. Although, by V1 (median 4 months [IQR 3-7] from disease onset), many acute-stage symptoms in participants with anti-NMDAR encephalitis had resolved (acute stage median modified Rankin Scale [mRS] score 5 [IQR 4-5] vs V1 mRS score 2 [1-2]; p<0·0001), 25 (89%) participants showed deficits in at least one cognitive domain. In this group, 15 (68%) of 22 cognitive domain variables were impaired at V1, whereas only eight (36%) were altered at V3 (p=0·016). In participants with schizophrenia spectrum disorders, 11 (50%) of 22 variables (all shared with participants with anti-NMDAR encephalitis) were impaired at V1, without changes at V3. Two acute-stage features of anti-NMDAR encephalitis (ie, decreased consciousness and no improvement within the first 4 weeks of treatment) predicted cognitive domain outcomes, and a visuospatial task (ie, serial biases) at V1 showed potential in predicting learning and memory outcomes. At V1, all psychiatric symptom clusters were similarly altered in participants with anti-NMDAR encephalitis and in those with schizophrenia spectrum disorders, but only those in individuals with anti-NMDAR encephalitis subsequently improved (p=0·031). The greatest cognitive-psychiatric improvement in participants with anti-NMDAR encephalitis occurred between V1 and V2. During this interval, four (14%) participants with anti-NMDAR encephalitis would have met the diagnostic criteria of schizophrenia if CSF antibody findings had not been investigated.The cognitive-psychiatric symptoms of anti-NMDAR encephalitis in the post-acute stage resembled those of stabilised schizophrenia, but only those in participants with anti-NMDAR encephalitis progressively improved, predominantly during V1-V2. These findings are important for clinical trials on anti-NMDAR encephalitis and suggest that prompt cognitive-psychosocial rehabilitation might be a valuable intervention.Instituto Salud Carlos III, NEURON Network of European Funding for Neuroscience Research, National Alliance for Research in Schizophrenia and Affective Disorders, and la Caixa Health-Research Foundation.