Escolar Maria L, Poe Michele D, Martin Holly R, Kurtzberg Joanne
Program for Neurodevelopmental Function in Rare Disorders, Clinical Center for the Study of Development and Learning, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7255, USA.
Pediatrics. 2006 Sep;118(3):e879-89. doi: 10.1542/peds.2006-0747. Epub 2006 Aug 21.
Infantile Krabbe disease, a rare neurodegenerative disorder that leads to rapid demyelination, dysmyelination, and death in the first 2 years of life, is responsive to treatment with umbilical cord blood transplantation provided that the patient is treated in the first weeks of life. At present, family history is the only way to identify patients that are asymptomatic with most patients being diagnosed after onset of symptoms. We hypothesized that a staging system based on clinical indicators and neurophysiological and neuroimaging measures can predict posttreatment variation in patients diagnosed with infantile Krabbe disease.
A retrospective review of pretransplant clinical indicators and neurodevelopmental, brain imaging and neurophysiological measures was performed in 42 patients being considered for treatment with umbilical cord blood transplantation. Based on these evaluations, an expert system approach was used to develop a staging system for infantile Krabbe disease. Another set of analyses in the subset of patients who were transplanted (n = 29) evaluated the association between pretransplant stage of disease and posttransplant neurodevelopmental outcomes.
A staging algorithm for infants with infantile Krabbe disease was developed and tested for predicting neurodevelopmental outcome after umbilical cord blood transplantation. Standard neurophysiological and neuroimaging tests were not useful in the staging algorithm. Clinical indicators were found to best classify stage of disease. Pretransplant stage was found to be predictive of neurodevelopmental outcome.
We conclude that the clinical staging system based solely on signs and symptoms of disease can be used to predict outcomes after umbilical cord blood transplantation. This staging system can be used prospectively to guide physicians unfamiliar with the disorder in evaluating, monitoring, and counseling families about treatment outcomes. The staging will be useful for both patients diagnosed with infantile Krabbe disease because of clinical symptoms and those identified through neonatal screening programs.
婴儿型克拉伯病是一种罕见的神经退行性疾病,会导致在生命的头两年内迅速出现脱髓鞘、髓鞘形成异常并死亡。若患者在生命的最初几周内接受治疗,脐带血移植治疗对此病有效。目前,家族病史是识别无症状患者的唯一方法,大多数患者在出现症状后才被诊断出来。我们假设基于临床指标以及神经生理学和神经影像学测量的分期系统可以预测婴儿型克拉伯病患者治疗后的变化情况。
对42名考虑接受脐带血移植治疗的患者移植前的临床指标以及神经发育、脑成像和神经生理学测量进行了回顾性分析。基于这些评估,采用专家系统方法开发了婴儿型克拉伯病的分期系统。对已接受移植的患者子集(n = 29)进行的另一组分析评估了移植前疾病分期与移植后神经发育结果之间的关联。
开发并测试了一种用于预测婴儿型克拉伯病婴儿脐带血移植后神经发育结果的分期算法。标准神经生理学和神经影像学检查在该分期算法中并无用处。发现临床指标最能对疾病分期进行分类。发现移植前分期可预测神经发育结果。
我们得出结论,仅基于疾病体征和症状的临床分期系统可用于预测脐带血移植后的结果。该分期系统可前瞻性地用于指导不熟悉该疾病的医生评估、监测并就治疗结果向家庭提供咨询。该分期对于因临床症状而被诊断为婴儿型克拉伯病的患者以及通过新生儿筛查项目识别出的患者均有用处。