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伊利诺伊州克拉贝病新生儿筛查经验:神经鞘氨醇在该疾病诊断中的作用

Newborn Screening for Krabbe Disease-Illinois Experience: Role of Psychosine in Diagnosis of the Disease.

作者信息

Basheeruddin Khaja, Shao Rong, Balster Fran, Gardley Pearlie, Ashbaugh Laura

机构信息

Newborn Screening Laboratory, Illinois Department of Public Health, Chicago, IL 60612, USA.

Office of Health Promotion, Illinois Department of Public Health, Springfield, IL 62671, USA.

出版信息

Int J Neonatal Screen. 2021 May 9;7(2):24. doi: 10.3390/ijns7020024.

Abstract

Population-based newborn screening for Krabbe disease was initiated by measurement of galactocerebrosidase (GALC) activity in the state of Illinois in December 2017. Due to the poor specificity of GALC for the diagnosis of Krabbe disease, second-tier testing services were provided to reduce the false positive rates for disease monitoring. Using ultra-pressure liquid chromatography coupled to mass spectrometry assay, a total of 497,147 newborns were screened. In total, 288 infants' specimens (0.06%) having reduced GALC activity were sent out for second-tier testing to a reference laboratory. All newborns' reduced GALC specimens were tested for psychosine levels, the presence of a 30-kb deletion and GALC sequencing. The results showed that two infants had elevated psychosine levels (10 and 35 nM) and were referred immediately for evaluation and treatment for Infantile Krabbe disease, and six infants had intermediate PSY levels (≥2 to 5 nM) and are under observation as suspected candidates for late-onset Krabbe disease. In addition, 178 infants had pseudodeficiency alleles, all having psychosine levels < 2.0 nM. Our data show that a high percentage of reduced GALC activity (62%) was due to the presence of pseudodeficiency alleles in the GALC gene. In conclusion, incorporation of psychosine measurements can identify infants with infantile Krabbe disease and probable late-onset Krabbe infants. Furthermore, Krabbe disease screening can be achieved at public health laboratories, and infants with infantile Krabbe disease can be diagnosed in timely manner for better outcome.

摘要

2017年12月,伊利诺伊州通过检测半乳糖脑苷脂酶(GALC)活性启动了基于人群的克拉伯病新生儿筛查。由于GALC对克拉伯病诊断的特异性较差,因此提供了二级检测服务以降低疾病监测的假阳性率。使用超高压液相色谱-质谱联用分析法,共筛查了497147名新生儿。共有288名婴儿的标本(0.06%)GALC活性降低,被送往参考实验室进行二级检测。所有GALC活性降低的新生儿标本均检测了精神鞘氨醇水平、30 kb缺失的存在情况以及GALC测序。结果显示,两名婴儿的精神鞘氨醇水平升高(分别为10和35 nM),被立即转诊以评估和治疗婴儿型克拉伯病,六名婴儿的精神鞘氨醇水平处于中间值(≥2至5 nM),作为晚发型克拉伯病疑似候选者正在接受观察。此外,178名婴儿存在假缺陷等位基因,其精神鞘氨醇水平均<2.0 nM。我们的数据表明,GALC活性降低的高比例(62%)是由于GALC基因中存在假缺陷等位基因。总之,纳入精神鞘氨醇测量可以识别婴儿型克拉伯病患儿以及可能的晚发型克拉伯病婴儿。此外,克拉伯病筛查可在公共卫生实验室实现,婴儿型克拉伯病患儿可得到及时诊断,从而获得更好的预后。

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