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澳大利亚儿科队列中首次脱髓鞘综合征后多发性硬化症的风险:临床、影像学特征及 McDonald 2010 MRI 标准的应用。

Risk of multiple sclerosis after a first demyelinating syndrome in an Australian Paediatric cohort: clinical, radiological features and application of the McDonald 2010 MRI criteria.

机构信息

Institute for Neuroscience and Muscle Research, The Children's Hospital at Westmead, University of Sydney, Australia.

出版信息

Mult Scler. 2013 Nov;19(13):1749-59. doi: 10.1177/1352458513484377. Epub 2013 Apr 11.

DOI:10.1177/1352458513484377
PMID:23579092
Abstract

BACKGROUND

The risk of multiple sclerosis (MS) is dependent on multiple variables, including geographical location. There is increasing interest in the early recognition and treatment of MS in children.

METHOD

Using univariate and multivariate analysis, we determined the clinical and radiological features that were predictive of MS in 88 children from New South Wales, Australia, with a first acute demyelinating syndrome (ADS) who were followed for a minimum of one year. We tested the McDonald, KIDMUS, Callen and Verhey MRI criteria for paediatric MS.

RESULTS

After a mean follow-up of 5.2 years, 13/88 (15%) of children had MS. Using multivariate analysis, preceding infection was protective of MS, and corpus callosal lesions, the combined presence of both well and poorly demarcated lesions, and contrast-enhancing lesions on MRI were predictive of MS. The sensitivity and specificity of the respective radiological criteria were McDonald 2005 (69%, 68%), McDonald 2010 (58%, 95%), KIDMUS (8%, 100%), Callen (69%, 85%) and Verhey (62%, 84%). When McDonald 2010 criteria were applied to baseline and serial scans, the sensitivity and specificity was 91% and 93%.

CONCLUSION

Despite the long follow-up, the risk of MS appears lower in New South Wales children compared to previously reported cohorts. Radiological features are more predictive than clinical features in predicting MS. The McDonald 2010 criteria performed well although the dissemination in time criteria on baseline scans is difficult to apply to children with encephalopathy.

摘要

背景

多发性硬化症(MS)的风险取决于多个变量,包括地理位置。人们越来越关注儿童 MS 的早期识别和治疗。

方法

我们使用单变量和多变量分析,确定了 88 名来自澳大利亚新南威尔士州的首发急性脱髓鞘综合征(ADS)患儿的临床和影像学特征,这些患儿至少随访 1 年,以预测 MS。我们测试了 McDonald、KIDMUS、Callen 和 Verhey 的儿科 MS MRI 标准。

结果

平均随访 5.2 年后,88 名儿童中有 13 名(15%)患有 MS。使用多变量分析,前驱感染对 MS 有保护作用,胼胝体病变、同时存在边界清楚和不清楚病变、MRI 上有增强病变是 MS 的预测因素。各自的放射学标准的敏感性和特异性为 McDonald 2005(69%,68%)、McDonald 2010(58%,95%)、KIDMUS(8%,100%)、Callen(69%,85%)和 Verhey(62%,84%)。当 McDonald 2010 标准应用于基线和系列扫描时,敏感性和特异性分别为 91%和 93%。

结论

尽管随访时间较长,但与之前报道的队列相比,新南威尔士州儿童的 MS 风险似乎较低。在预测 MS 方面,影像学特征比临床特征更具预测性。McDonald 2010 标准表现良好,尽管在基线扫描上应用时间分布标准对脑病患儿来说具有一定难度。

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