Comparative Study of Paraneoplastic and Nonparaneoplastic Autoimmune Encephalitis With GABABR Antibodies.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY Neurology® Neuroimmunology & Neuroinflammation Pub Date : 2024-05-01 Epub Date: 2024-04-24 DOI:10.1212/NXI.0000000000200229
Florian Lamblin, Jeroen Kerstens, Sergio Muñiz-Castrillo, Alberto Vogrig, David Goncalves, Veronique Rogemond, Geraldine Picard, Marine Villard, Anne-Laurie Pinto, Marleen H Van Coevorden-Hameete, Marienke A De Bruijn, Juna M De Vries, Marco Schreurs, Louise Tyvaert, Lucie Hopes, Jerome Aupy, Cecile Marchal, Dimitri Psimaras, Laurent Kremer, Veronique Bourg, Jean-Christophe G Antoine, Adrien Wang, Philippe Kahane, Sophie Demeret, Guido Ahle, Vicente Peris Sempere, Noemie Timestit, Mikail Nourredine, Aurelien Maureille, Marie Benaiteau, Bastien Joubert, Emmanuel Mignot, Maarten J Titulaer, Jerome Honnorat
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引用次数: 0

Abstract

Background and objectives: While patients with paraneoplastic autoimmune encephalitis (AE) with gamma-aminobutyric-acid B receptor antibodies (GABABR-AE) have poor functional outcomes and high mortality, the prognosis of nonparaneoplastic cases has not been well studied.

Methods: Patients with GABABR-AE from the French and the Dutch Paraneoplastic Neurologic Syndromes Reference Centers databases were retrospectively included and their data collected; the neurologic outcomes of paraneoplastic and nonparaneoplastic cases were compared. Immunoglobulin G (IgG) isotyping and human leukocyte antigen (HLA) genotyping were performed in patients with available samples.

Results: A total of 111 patients (44/111 [40%] women) were enrolled, including 84 of 111 (76%) paraneoplastic and 18 of 111 (16%) nonparaneoplastic cases (cancer status was undetermined for 9 patients). Patients presented with seizures (88/111 [79%]), cognitive impairment (54/111 [49%]), and/or behavioral disorders (34/111 [31%]), and 54 of 111 (50%) were admitted in intensive care unit (ICU). Nonparaneoplastic patients were significantly younger (median age 54 years [range 19-88] vs 67 years [range 50-85] for paraneoplastic cases, p < 0.001) and showed a different demographic distribution. Nonparaneoplastic patients more often had CSF pleocytosis (17/17 [100%] vs 58/78 [74%], p = 0.02), were almost never associated with KTCD16-abs (1/16 [6%] vs 61/70 [87%], p < 0.001), and were more frequently treated with second-line immunotherapy (11/18 [61%] vs 18/82 [22%], p = 0.003). However, no difference of IgG subclass or HLA association was observed, although sample size was small (10 and 26 patients, respectively). After treatment, neurologic outcome was favorable (mRS ≤2) for 13 of 16 (81%) nonparaneoplastic and 37 of 84 (48%) paraneoplastic cases (p = 0.03), while 3 of 18 (17%) and 42 of 83 (51%) patients had died at last follow-up (p = 0.008), respectively. Neurologic outcome no longer differed after adjustment for confounding factors but seemed to be negatively associated with increased age and ICU admission. A better survival was associated with nonparaneoplastic cases, a younger age, and the use of immunosuppressive drugs.

Discussion: Nonparaneoplastic GABABR-AE involved younger patients without associated KCTD16-abs and carried better neurologic and vital prognoses than paraneoplastic GABABR-AE, which might be due to a more intensive treatment strategy. A better understanding of immunologic mechanisms underlying both forms is needed.

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副肿瘤性和非副肿瘤性自身免疫性脑炎与 GABABR 抗体的比较研究
背景和目的:伴有γ-氨基丁酸B受体抗体(GABABR-AE)的副肿瘤性自身免疫性脑炎(AE)患者的功能预后差、死亡率高,而对非副肿瘤性病例的预后尚未进行深入研究:方法:回顾性纳入法国和荷兰副肿瘤性神经系统综合征参考中心数据库中的GABABR-AE患者并收集其数据;比较副肿瘤性和非副肿瘤性病例的神经系统预后。对有样本的患者进行了免疫球蛋白G(IgG)同型和人类白细胞抗原(HLA)基因分型:共有 111 名患者(44/111 [40%] 女性)入组,其中包括 111 例副肿瘤性病例中的 84 例(76%)和 111 例非副肿瘤性病例中的 18 例(16%)(9 例患者的癌症状态未确定)。患者表现为癫痫发作(88/111 [79%])、认知障碍(54/111 [49%])和/或行为障碍(34/111 [31%]),111 例患者中有 54 例(50%)入住重症监护室(ICU)。非副肿瘤性患者明显更年轻(中位年龄为 54 岁 [19-88 岁] ,副肿瘤性病例为 67 岁 [50-85 岁],P < 0.001),并且呈现出不同的人口分布。非副肿瘤性患者更常见 CSF 多细胞增多(17/17 [100%] vs 58/78 [74%],p = 0.02),几乎从未伴有 KTCD16-abs(1/16 [6%] vs 61/70 [87%],p < 0.001),更常接受二线免疫治疗(11/18 [61%] vs 18/82 [22%],p = 0.003)。不过,虽然样本量较少(分别为 10 例和 26 例患者),但未观察到 IgG 亚类或 HLA 相关性的差异。治疗后,16 例非副肿瘤性病例中有 13 例(81%)和 84 例副肿瘤性病例中有 37 例(48%)的神经功能预后良好(mRS ≤2)(p = 0.03),而在最后一次随访时,18 例患者中有 3 例(17%)死亡,83 例患者中有 42 例(51%)死亡(p = 0.008)。在对混杂因素进行调整后,神经系统结果不再存在差异,但似乎与年龄增加和入住重症监护室呈负相关。非副肿瘤性病例、年龄较小及使用免疫抑制剂的病例存活率较高:讨论:非副肿瘤性GABABR-AE的患者年龄较小,且不伴有KCTD16-abs,其神经系统和生命预后优于副肿瘤性GABABR-AE,这可能是由于采用了更强化的治疗策略。我们需要更好地了解这两种形式的免疫机制。
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来源期刊
CiteScore
15.60
自引率
2.30%
发文量
219
审稿时长
8 weeks
期刊介绍: Neurology Neuroimmunology & Neuroinflammation is an official journal of the American Academy of Neurology. Neurology: Neuroimmunology & Neuroinflammation will be the premier peer-reviewed journal in neuroimmunology and neuroinflammation. This journal publishes rigorously peer-reviewed open-access reports of original research and in-depth reviews of topics in neuroimmunology & neuroinflammation, affecting the full range of neurologic diseases including (but not limited to) Alzheimer's disease, Parkinson's disease, ALS, tauopathy, and stroke; multiple sclerosis and NMO; inflammatory peripheral nerve and muscle disease, Guillain-Barré and myasthenia gravis; nervous system infection; paraneoplastic syndromes, noninfectious encephalitides and other antibody-mediated disorders; and psychiatric and neurodevelopmental disorders. Clinical trials, instructive case reports, and small case series will also be featured.
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