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通过串联质谱法对干血斑中的酶进行直接多重检测用于溶酶体贮积症的新生儿筛查。

Direct multiplex assay of enzymes in dried blood spots by tandem mass spectrometry for the newborn screening of lysosomal storage disorders.

作者信息

Gelb Michael H, Turecek Frantisek, Scott C Ron, Chamoles Nestor A

机构信息

Department of Chemistry, University of Washington, Seattle, Washington, USA.

出版信息

J Inherit Metab Dis. 2006 Apr-Jun;29(2-3):397-404. doi: 10.1007/s10545-006-0265-4.

Abstract

Tandem mass spectrometry is currently used in newborn screening programmes to quantify the level of amino acids and acylcarnitines in dried blood spots for detection of metabolites associated with treatable diseases. We have developed assays for lysosomal enzymes in rehydrated dried blood spots in which a set of substrates is added and the set of corresponding enzymatic products are quantified using tandem mass spectrometry with the aid of mass-differentiated internal standards. We have developed a multiplex assay of the set of enzymes that, when deficient, cause the lysosomal storage disorders Fabry, Gaucher, Hurler, Krabbe, Niemann-Pick A/B and Pompe diseases. These diseases were selected because treatments are now available or expected to emerge shortly. The discovery that acarbose is a selective inhibitor of maltase glucoamylase allows the Pompe disease enzyme, acid alpha-glucosidase, to be selectively assayed in white blood cells and dried blood spots. When tested with dried blood spots from 40 unaffected individuals and 10-12 individuals with the lysosomal storage disorder, the tandem mass spectrometry assay led to the correct identification of the affected individuals with 100% sensitivity. Many of the reagents needed for the new assays are commercially available, and those that are not are being prepared under Good Manufacturing Procedures for approval by the FDA. Our newborn screening assay for Krabbe disease is currently being put in place at the Wadsworth Center in New York State for the analysis of approximately 1000 dried blood spots per day. Summary We have developed tandem mass spectrometry for the direct assay of lysosomal enzymes in rehydrated dried blood spots that can be implemented for newborn screening of lysosomal storage disorders. Several enzymes can be analysed by a single method (multiplex analysis) and in a high-throughput manner appropriate for newborn screening laboratories.

摘要

串联质谱目前用于新生儿筛查项目,以定量干血斑中氨基酸和酰基肉碱的水平,用于检测与可治疗疾病相关的代谢物。我们已经开发了用于复水干血斑中溶酶体酶的检测方法,其中添加一组底物,并使用串联质谱借助质量区分内标对相应的酶产物组进行定量。我们已经开发了一组酶的多重检测方法,这些酶缺乏时会导致溶酶体贮积症,如法布里病、戈谢病、胡尔勒病、克拉贝病、尼曼-皮克A/B病和庞贝病。选择这些疾病是因为现在已有治疗方法或预计不久将会出现。发现阿卡波糖是麦芽糖酶葡糖淀粉酶的选择性抑制剂,这使得可以在白细胞和干血斑中选择性地检测庞贝病酶,即酸性α-葡萄糖苷酶。当用来自40名未受影响个体和10 - 12名患有溶酶体贮积症个体的干血斑进行测试时,串联质谱检测以100%的灵敏度正确识别出受影响的个体。新检测所需的许多试剂都有商业供应,那些没有的正在按照良好生产规范制备,以待美国食品药品监督管理局批准。我们针对克拉贝病的新生儿筛查检测目前正在纽约州的沃兹沃思中心开展,每天分析约1000个干血斑。总结 我们已经开发出串联质谱法,用于直接检测复水干血斑中的溶酶体酶,可用于新生儿溶酶体贮积症的筛查。几种酶可以通过单一方法(多重分析)并以适合新生儿筛查实验室的高通量方式进行分析。

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