首页> 外文期刊>Clinical Chemistry: Journal of the American Association for Clinical Chemists >Tandem Mass Spectrometry Has a Larger Analytical Range than Fluorescence Assays of Lysosomal Enzymes: Application to Newborn Screening and Diagnosis of Mucopolysaccharidoses Types II, IVA, and VI
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Tandem Mass Spectrometry Has a Larger Analytical Range than Fluorescence Assays of Lysosomal Enzymes: Application to Newborn Screening and Diagnosis of Mucopolysaccharidoses Types II, IVA, and VI

机译:串联质谱法比溶酶体酶的荧光分析法具有更大的分析范围:在II型,IVA型和VI型粘多糖酶的新生儿筛查和诊断中的应用

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BACKGROUND: There is interest in newborn screening and diagnosis of lysosomal storage diseases because of the development of treatment options that improve clinical outcome. Assays of lysosomal enzymes with high analytical range (ratio of assay response from the enzymatic reaction divided by the assay response due to nonenzymatic processes) are desirable because they are predicted to lead to a lower rate of false positives in population screening and to more accurate diagnoses.METHODS: We designed new tandem mass spectrometry (MS/MS) assays that give the largest analytical ranges reported to date for the use of dried blood spots (DBS) for detection of mucopolysaccharidoses type II (MPS-II), MPS-IVA, and MPS-VI. For comparison, we carried out fluorometric assays of 6 lysosomal enzymes using 4-methylumbelliferyl (4MU)-substrate conjugates.RESULTS: The MS/MS assays for MPS-II, -IVA, and -VI displayed analytical ranges that are 1–2 orders of magnitude higher than those for the corresponding fluorometric assays. The relatively small analytical ranges of the 4MU assays are due to the intrinsic fluorescence of the 4MU substrates, which cause high background in the assay response.CONCLUSIONS: These highly reproducible MS/MS assays for MPS-II, -IVA, and -VI can support multiplex newborn screening of these lysosomal storage diseases. MS/MS assays of lysosomal enzymes outperform 4MU fluorometric assays in terms of analytical range. Ongoing pilot studies will allow us to gauge the impact of the increased analytical range on newborn screening performance.
机译:背景:由于开发了可改善临床结局的治疗选择,人们对新生儿的溶酶体贮积病筛查和诊断感兴趣。具有较高分析范围的溶酶体酶测定(酶促反应的测定应答比率除以非酶促过程引起的测定应答的比率)是可取的,因为预计它们会导致群体筛选中假阳性的发生率降低,并且诊断更加准确方法:我们设计了新的串联质谱(MS / MS)分析方法,该方法提供了迄今为止报道的最大分析范围,可用于使用干血斑(DBS)检测II型黏多糖多糖(MPS-II),MPS-IVA,和MPS-VI。为了进行比较,我们使用4-甲基伞形酮(4MU)-底物偶联物对6种溶酶体酶进行了荧光分析。结果:MPS-II,-IVA和-VI的MS / MS分析显示的分析范围为1-2个数量级的数量级高于相应的荧光测定法。 4MU分析的相对较小的分析范围归因于4MU底物的固有荧光,这导致了分析响应中的高背景。结论:这些用于MPS-II,-IVA和-VI的高重现性MS / MS分析可以支持对这些溶酶体贮积病进行多重新生儿筛查。就分析范围而言,溶酶体酶的MS / MS分析优于4MU荧光分析。正在进行的试点研究将使我们能够评估增加的分析范围对新生儿筛查性能的影响。

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