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串联质谱技术改变代谢物检测和新生儿筛查:从实验室到临床的经验教训。

Altered metabolism and newborn screening using tandem mass spectrometry: lessons learned from the bench to bedside.

机构信息

Pediatrix Center for Research, Education and Quality, Pediatrix Medical Group, 1301 Concord Terrace Sunrise, FL 33323, USA.

出版信息

Curr Pharm Biotechnol. 2011 Jul;12(7):965-75. doi: 10.2174/138920111795909104.

DOI:10.2174/138920111795909104
PMID:21466463
Abstract

The use of tandem mass spectrometry (MS/MS) for screening of inherited metabolic disease in newborns has afforded many unique opportunities in the understanding of the benefits early their early detection, diagnosis and treatment. From the standpoint of the laboratory and modern analytical methods, the use of MS based analysis demonstrated that a multiple metabolite-multiple disease screen-one method approach expanded screening significantly. MS/MS and newborn screening has served as a model of one type of approach in preventative health care that has shown proven benefits. It has been nearly 20 years since the introduction of MS/MS analysis of dried blood spots from newborns. There have been many lessons learned in both the analytical approach as well as follow-up at the bedside. These lessons can be applied to future applications of MS/MS in newborn screening as well as other areas of metabolism and metabolic profiles such as that from acquired disease, environmental disease and other factors such as nutrition and age. The use of a highly specific, sensitive and multiplex platform such as MS/MS will continue to grow and experience in the newborn screening application will insure this outcome.

摘要

串联质谱(MS/MS)在新生儿遗传代谢病筛查中的应用,为我们了解早期检测、诊断和治疗的益处提供了许多独特的机会。从实验室和现代分析方法的角度来看,基于 MS 的分析方法表明,一种多代谢物-多种疾病的筛查方法可以显著扩大筛查范围。MS/MS 和新生儿筛查已经成为预防性保健的一种模式,已经证明了其益处。自新生儿干血斑的 MS/MS 分析引入以来,已经过去了将近 20 年。在分析方法和床边随访方面都吸取了很多经验教训。这些经验教训可以应用于未来 MS/MS 在新生儿筛查以及代谢和代谢谱的其他领域的应用,例如获得性疾病、环境疾病以及营养和年龄等其他因素。MS/MS 等高度特异性、高灵敏度和多重检测平台的应用将继续增长,新生儿筛查应用的经验将确保这一结果。

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