Department of Pediatrics, Division of Child and Adolescent Neurology, Southern Illinois University, Springfield, Illinois.
Pediatr Neurol. 2013 Nov;49(5):329-34. doi: 10.1016/j.pediatrneurol.2013.06.023. Epub 2013 Aug 27.
To evaluate the practical application of International Pediatrics Multiple Sclerosis study group definitions in children with inflammatory demyelination of the central nervous system and to identify predictors of multiple sclerosis.
Baseline data on 123 children with a first episode of acute central nervous system demyelination were collected. The initial diagnosis according to the International Pediatrics Multiple Sclerosis study group was recorded and compared with final diagnosis.
Forty-seven (38.2%) children met International Pediatrics Multiple Sclerosis study group criteria for acute disseminated encephalomyelitis and 67 (54.4%) had clinically isolated syndrome at the initial presentation. Four (3.2%) had the diagnosis of neuromyelitis optica and five (4%) did not meet any specific diagnosis per the study group criteria. Clinical follow-up was available on 118 of 123 children (95.9%), with a median of 61.5 months (quartile range 23, 110 months). Conversion from clinically isolated syndrome to multiple sclerosis occurred in 26 of 67 children (38.8%); acute disseminated encephalomyelitis to multiple sclerosis occurred in 4 of 47 children (8.5%). Adjusted multivariate logistic regression analysis for an outcome of future development of multiple sclerosis showed the following predictors: female gender (odds ratio 12.44; 95% confidence interval 1.03-149.3); initial diagnosis of monofocal brain stem or hemispheric dysfunction (odds ratio 24.57; 95% confidence interval 3.06-196.78); and Callen magnetic resonance imaging criteria if met (odds ratio 122.45; 95% confidence interval 16.57-904.57).
International Pediatrics Multiple Sclerosis study group criteria affirm that children with initial clinically isolated syndrome are more likely to develop future multiple sclerosis compared with those with an acute disseminated encephalomyelitis initial diagnosis. In addition, female gender, brain stem or hemispheric involvement, and Callen magnetic resonance imaging criteria predict the diagnosis of multiple sclerosis.
评估国际儿科多发性硬化症研究组(International Pediatrics Multiple Sclerosis study group,IPMSSG)定义在儿童中枢神经系统炎症性脱髓鞘疾病中的实际应用,并确定多发性硬化症的预测因素。
收集了 123 例首发急性中枢神经系统脱髓鞘患儿的基线资料。记录了根据 IPMSSG 作出的初始诊断,并与最终诊断进行了比较。
47 例(38.2%)患儿符合急性播散性脑脊髓炎的 IPMSSG 标准,67 例(54.4%)患儿在首发时表现为临床孤立综合征。4 例(3.2%)患儿诊断为视神经脊髓炎,5 例(4%)患儿不符合 IPMSSG 标准的任何特定诊断。123 例患儿中有 118 例(95.9%)获得了临床随访,中位随访时间为 61.5 个月(四分位距 23,110 个月)。67 例临床孤立综合征患儿中有 26 例(38.8%)发展为多发性硬化症,47 例急性播散性脑脊髓炎患儿中有 4 例(8.5%)发展为多发性硬化症。对多发性硬化症未来发展结局进行调整后的多变量逻辑回归分析显示,以下因素是预测指标:女性(比值比 12.44;95%置信区间 1.03-149.3)、首发为单灶性脑干或半球功能障碍(比值比 24.57;95%置信区间 3.06-196.78)、符合 Callen 磁共振成像标准(比值比 122.45;95%置信区间 16.57-904.57)。
IPMSSG 标准证实,与急性播散性脑脊髓炎初始诊断相比,初始表现为临床孤立综合征的患儿更有可能发展为未来的多发性硬化症。此外,女性、脑干或半球受累、Callen 磁共振成像标准可预测多发性硬化症的诊断。