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儿童和青少年的精神自身免疫性疾病:紧张症是严重程度的标志吗?

Psychiatric autoimmune conditions in children and adolescents: Is catatonia a severity marker?

机构信息

Department of Child and Adolescent Psychiatry, Sorbonne Université, Hôpital Pitié-Salpêtrière, AP-HP, 47-83 Boulevard de l'Hôpital, 75013 Paris, France; Department of Child and Adolescent Psychiatry, Université de Rouen, Hôpital Charles Nicolle, 1 rue de Germont, 76000 Rouen, France.

Department of Child and Adolescent Psychiatry, Hôpital Universitaire d'Angers, 4 Rue Larrey, 49100 Angers, France.

出版信息

Prog Neuropsychopharmacol Biol Psychiatry. 2021 Jan 10;104:110028. doi: 10.1016/j.pnpbp.2020.110028. Epub 2020 Jul 1.

Abstract

OBJECTIVES

Patients with autoimmune encephalitis (AE) are likely to exhibit an acute onset of severe psychiatric features, including psychosis and/or catatonia. Based on the high prevalence of catatonia in AE and our clinical experience, we hypothesized that catatonia might be a marker of severity requiring more aggressive treatment approaches.

METHODS

To reach a sufficient number of cases with brain-autoimmune conditions, we pooled two samples (N = 58): the first from the French National Network of Rare Psychiatric diseases and the second from the largest Italian neuro-pediatrics center for encephalopathies. Autoimmune conditions were diagnosed using a multidisciplinary approach and numerous paraclinical investigations. We retrospectively compared patients with and without catatonia for psychiatric and non-psychiatric clinical features, biological and imaging assessments, type of immunotherapy used and outcomes.

RESULTS

The sample included 25 patients (43%) with catatonia and 33 (57%) without catatonia. Forty-two patients (72.4%) had a definite AE (including 27 anti-NMDA receptor encephalitis) and 16 (27.6%) suspected autoimmune encephalitis. Patients with catatonia showed significantly more psychotic features [18 (72%) vs 9 (27.3%), p < 0.001)] and more movement disorders [25 (100%) vs 20 (60.6%), p < 0.001] than patients without catatonia. First line (corticoids, immunoglobulin and plasma exchanges) and second line (e.g., rituximab) therapies were more effective in patients with catatonia, with 24 (96%) vs 22 (66.7%) (p = 0.006) and 17 (68%) vs 9 (27.3%) (p = 0.002), respectively. However, those with catatonia received more combinations of first and second line treatments and had more relapses during outcomes.

CONCLUSION

Despite its exploratory design, the study supports the idea that autoimmune catatonia may be a marker of severity and morbidity in terms of initial presentation and relapses, requiring the need for early and aggressive treatment.

摘要

目的

自身免疫性脑炎(AE)患者可能表现出严重精神病特征的急性发作,包括精神病和/或紧张症。基于 AE 中紧张症的高患病率和我们的临床经验,我们假设紧张症可能是需要更积极治疗方法的严重程度标志物。

方法

为了达到具有脑自身免疫疾病的足够病例数,我们汇集了两个样本(N=58):第一个来自法国罕见精神病学疾病网络,第二个来自意大利最大的神经儿科脑病中心。使用多学科方法和许多临床前检查来诊断自身免疫性疾病。我们回顾性比较了有和没有紧张症的患者的精神病和非精神病临床特征、生物学和影像学评估、使用的免疫疗法类型和结局。

结果

该样本包括 25 名(43%)有紧张症的患者和 33 名(57%)没有紧张症的患者。42 名(72.4%)患者有明确的 AE(包括 27 名抗 NMDA 受体脑炎)和 16 名(27.6%)疑似自身免疫性脑炎。有紧张症的患者表现出明显更多的精神病特征[18 名(72%)比 9 名(27.3%),p<0.001]和更多的运动障碍[25 名(100%)比 20 名(60.6%),p<0.001]。与没有紧张症的患者相比,一线(皮质类固醇、免疫球蛋白和血浆置换)和二线(如利妥昔单抗)治疗更有效,分别有 24 名(96%)比 22 名(66.7%)(p=0.006)和 17 名(68%)比 9 名(27.3%)(p=0.002)。然而,那些有紧张症的患者接受了更多的一线和二线治疗组合,并且在结局期间有更多的复发。

结论

尽管设计为探索性,该研究支持自身免疫性紧张症可能是初始表现和复发方面严重程度和发病率的标志物的观点,需要早期和积极的治疗。

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