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A Novel Tandem Mass Spectrometry Method for Rapid Confirmation of Medium- and Very Long-Chain acyl-CoA Dehydrogenase Deficiency in Newborns

机译:快速确认新生儿中链和长链酰基辅酶A脱氢酶缺乏症的新型串联质谱方法

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摘要

BackgroundNewborn screening for medium- and very long-chain acyl-CoA dehydrogenase (MCAD and VLCAD, respectively) deficiency, using acylcarnitine profiling with tandem mass spectrometry, has increased the number of patients with fatty acid oxidation disorders due to the identification of additional milder, and so far silent, phenotypes. However, especially for VLCADD, the acylcarnitine profile can not constitute the sole parameter in order to reliably confirm disease. Therefore, we developed a new liquid chromatography tandem mass spectrometry (LC-MS/MS) method to rapidly determine both MCAD- and/or VLCAD-activity in human lymphocytes in order to confirm diagnosis.
机译:背景技术使用酰基肉碱轮廓分析和串联质谱法对中链和超长链酰基辅酶A脱氢酶(分别为MCAD和VLCAD)进行新生儿筛查,由于鉴定出其他轻度脂肪酸,增加了患有脂肪酸氧化障碍的患者人数,到目前为止,没有表现型。但是,尤其对于VLCADD,酰基肉碱谱不能构成唯一的参数以可靠地确认疾病。因此,我们开发了一种新的液相色谱串联质谱法(LC-MS / MS),以快速确定人淋巴细胞中的MCAD和/或VLCAD活性,从而确定诊断。

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