Clinical and radiological characteristics of MOG antibody-associated disease (MOGAD): a comparative study between pediatric and adult cohorts.

IF 2 4区 医学 Q3 CLINICAL NEUROLOGY
Ahmet Kasim Kilic, Hanife Senturk, Safiye Gunes Sager
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引用次数: 0

Abstract

Objective: Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is a distinct inflammatory demyelinating disorder As being first national study of pediatric and adult Turkish MOGAD patients so we aimed to report the clinical presentations, radiological findings, and relapse characteristics between pediatric and adult patients with MOGAD.

, materials and methods: In this retrospective study, 26 patients (10 pediatric [≤ 17 years] and 16 adult [> 17 years]) who tested positive for MOG antibodies were included. Demographic data, precipitating factors, Expanded Disability Status Scale (EDSS) scores, cerebrospinal fluid (CSF) findings, and magnetic resonance imaging (MRI) features were analyzed.

Results: The mean age was 10.8 years for children and 32.5 years for adults. Precipitating factors, primarily upper respiratory infections, were more frequent in children (70% vs. 12.5%). Pediatric patients predominantly presented with polysymptomatic onset, including pyramidal signs (60%) and encephalopathy (30%), whereas adults most commonly presented with optic neuritis (62.5%). Although adults had higher mean EDSS scores during relapse compared to children (4.31 vs. 3.55), final follow-up EDSS scores were low for both groups (0.78 vs. 0.5). Relapses were recorded only in the adult group (mean rate 1.93). Radiologically, children showed significantly higher rates of brainstem (34.6% vs. 7.6%) and cortical involvement. Spinal MRI revealed the "H-sign" in both groups, but conus involvement was more prevalent in children (75% vs. 7.6%).

Conclusion: MOGAD exhibits age-dependent clinical and radiological phenotypes. While pediatric cases often follow a post-infectious, polysymptomatic, and monophasic course, adult cases frequently present as optic neuritis with a higher tendency for relapse. Despite significant acute disability, functional recovery at the last visit was favorable in both populations over a mean follow-up of 24.1 ± 8.2 months in children and 33.6 ± 36.7 months in adults.

MOG抗体相关疾病(MOGAD)的临床和放射学特征:儿童和成人队列的比较研究
目的:髓鞘少突胶质细胞糖蛋白抗体相关疾病(MOGAD)是一种独特的炎症性脱髓鞘疾病。作为首个针对土耳其儿童和成人MOGAD患者的全国性研究,我们旨在报告儿童和成人MOGAD患者的临床表现、影像学表现和复发特征。材料与方法:本回顾性研究纳入26例MOG抗体阳性患者(10例儿童[≤17岁],16例成人[bb0 17岁])。分析了人口统计数据、诱发因素、扩展残疾状态量表(EDSS)评分、脑脊液(CSF)检查结果和磁共振成像(MRI)特征。结果:儿童平均年龄10.8岁,成人平均年龄32.5岁。诱发因素,主要是上呼吸道感染,在儿童中更为常见(70%对12.5%)。儿童患者主要表现为多症状,包括锥体体征(60%)和脑病(30%),而成人最常表现为视神经炎(62.5%)。虽然与儿童相比,成人在复发期间的平均EDSS评分较高(4.31比3.55),但两组的最终随访EDSS评分均较低(0.78比0.5)。仅成年组有复发记录(平均1.93)。放射学上,儿童的脑干受累率(34.6%比7.6%)和皮质受累率明显更高。脊柱MRI显示两组均有“h征”,但儿童中圆锥受累更普遍(75%对7.6%)。结论:MOGAD表现出年龄依赖性的临床和放射学表型。虽然儿童病例通常遵循感染后,多症状和单相病程,成人病例经常表现为视神经炎,复发倾向较高。尽管有明显的急性残疾,但在儿童平均随访24.1±8.2个月,成人平均随访33.6±36.7个月后,两组患者在最后一次就诊时功能恢复良好。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Acta neurologica Belgica
Acta neurologica Belgica 医学-临床神经学
CiteScore
4.20
自引率
3.70%
发文量
300
审稿时长
6-12 weeks
期刊介绍: Peer-reviewed and published quarterly, Acta Neurologica Belgicapresents original articles in the clinical and basic neurosciences, and also reports the proceedings and the abstracts of the scientific meetings of the different partner societies. The contents include commentaries, editorials, review articles, case reports, neuro-images of interest, book reviews and letters to the editor. Acta Neurologica Belgica is the official journal of the following national societies: Belgian Neurological Society Belgian Society for Neuroscience Belgian Society of Clinical Neurophysiology Belgian Pediatric Neurology Society Belgian Study Group of Multiple Sclerosis Belgian Stroke Council Belgian Headache Society Belgian Study Group of Neuropathology
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