Distinguishing Transient From Persistent Brain Structural Changes in Pediatric Patients With Acute Disseminated Encephalomyelitis.

IF 7.8 1区 医学 Q1 CLINICAL NEUROLOGY
Jason Michael Millward, Elias Pilgrim, Matthias Baumann, Eva-Maria Wendel, Ines El Naggar, Annikki Bertolini, Frederik Bartels, Carsten Finke, Friedemann Paul, Thoralf Niendorf, Kevin Rostásy, Sonia Waiczies
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引用次数: 0

Abstract

Background and objectives: Pediatric patients with acute disseminated encephalomyelitis (ADEM) are at risk of impaired brain growth, with long-term neuropsychiatric consequences. We previously reported transient expansions of cerebral ventricle volume (VV) in experimental autoimmune encephalomyelitis, which subsequently normalized. In this study, we investigated changes in VV in ADEM in relation to other brain structures and clinical outcomes.

Methods: We investigated brain MRI scans acquired in routine clinical practice from a multicenter cohort of 61 pediatric patients with ADEM, of whom 39 were myelin oligodendrocyte glycoprotein (MOG) antibody-positive. Patients were compared with 1,219 pediatric healthy controls (HCs). Volumes of multiple brain structures were computed using a contrast-agnostic machine learning-based tool and analyzed with mixed-effect models regarding other clinical parameters.

Results: Patients with ADEM had larger VV than HCs at initial clinical presentation, before immune therapy. Most of the patients showed further VV increases within 2 months after disease onset. Patients had smaller brain volumes than HCs, with specific reductions in deep gray matter structures. These changes were more pronounced in MOG antibody-negative patients.Of the patients with more than 2 MRI scans, 12 of 22 resolved their VV expansion back to within 15% of baseline values while 10 of 22 had persistently increased VV at the last available MRI within 1 year from onset. Patients with persistent VV expansion had greater reductions in volumes of other brain structures at the last MRI than patients whose VV resolved and were more likely to have residual neurologic signs. The VV resolving and nonresolving patients did not differ regarding age, sex, elevated CSF cell counts at baseline, or occurrence of relapses. However, patients with a larger magnitude of VV expansion-≥90% of baseline volume-were more likely to be in the nonresolving group.

Discussion: We could distinguish between 2 outcomes of VV changes in ADEM: one in which the VV expanded but ultimately returned to normal and one in which the expansions continued after disease onset and treatment but failed to resolve. The latter was associated with reduced brain volume, particularly in deep gray matter structures. This highlights the necessity for patients with ADEM to undergo regular MRI scans to assess whether developing VV expansions indicate a greater risk of permanent brain atrophy.

区分儿童急性播散性脑脊髓炎患者短暂性和持续性脑结构改变。
背景和目的:急性播散性脑脊髓炎(ADEM)患儿存在脑发育受损的风险,并具有长期的神经精神后果。我们之前报道了实验性自身免疫性脑脊髓炎患者脑室体积(VV)的短暂扩张,随后恢复正常。在这项研究中,我们研究了ADEM中VV的变化与其他脑结构和临床结果的关系。方法:我们研究了在常规临床实践中获得的61例小儿ADEM患者的脑MRI扫描,其中39例髓鞘少突胶质细胞糖蛋白(MOG)抗体阳性。将患者与1,219名儿童健康对照(hc)进行比较。使用基于对比不可告人的机器学习工具计算多个脑结构的体积,并使用混合效应模型分析其他临床参数。结果:在免疫治疗前,ADEM患者在初始临床表现时VV大于hc。大多数患者在发病后2个月内VV进一步升高。患者的脑容量比hc小,深度灰质结构明显减少。这些变化在MOG抗体阴性患者中更为明显。在接受2次以上MRI扫描的患者中,22人中有12人的VV扩张恢复到基线值的15%以内,而22人中有10人在发病后1年内的最后一次MRI检查中VV持续增加。与VV消退的患者相比,持续性VV扩张的患者在最后一次MRI检查中其他脑结构的体积减少更大,并且更可能有残留的神经系统体征。VV消退和非消退患者在年龄、性别、基线时脑脊液细胞计数升高或复发发生率方面没有差异。然而,VV扩张幅度较大(≥基线容量的90%)的患者更有可能属于非消退组。讨论:我们可以区分ADEM中VV变化的两种结果:一种是VV扩张但最终恢复正常,另一种是疾病发作和治疗后继续扩张但未能解决。后者与脑容量减少有关,尤其是在深部灰质结构中。这强调了对ADEM患者进行定期MRI扫描的必要性,以评估发生VV扩张是否表明永久性脑萎缩的风险更大。
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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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