干血斑液相色谱串联质谱法快速测定甲基丙二酸、丙酰肉碱和总同型半胱氨酸的临床应用

Q3 Medicine
Hiroyuki Iijima, Nobuyuki Ishige, M. Kubota
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引用次数: 1

摘要

甲基丙二酸血症(MMA)应在婴儿期早期诊断并在诊断后及时接受适当的治疗,以防止严重并发症导致死亡。目前,一种新生儿筛查(NBS)方法采用串联质谱法(MS/MS)通过升高丙酰基肉碱来鉴定疑似MMA患者。此外,采用干血斑的液相色谱串联质谱法(LC/MS/MS)作为二级检测,可有效检测部分代谢物,降低了NBS的假阳性率。然而,这些测试仅用于筛选,而不是用于评估治疗的检查。在此,我们描述了一个57天的MMA女孩在钴胺素治疗下尿甲基丙二酸水平升高。我们采用分离柱的LC/MS/MS方法评估她的钴胺素反应性,并比使用其他方法更早地发现钴胺素剂量不足。根据目前的资料,该方法似乎适用于MMA患者治疗的随访。然而,这应该通过更多的病例和更广泛的疾病谱来证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Application of Liquid Chromatography Tandem Mass Spectrometry Using Dried Blood Spot as a More Rapid Method for Determination of Methylmalonic Acid, Propionylcarnitine, and Total Homocysteine
Methylmalonic acidemia (MMA) should be diagnosed in early infancy and receive appropriate management promptly after the diagnosis to prevent severe complications leading to death. At present, a newborn screening (NBS) method using tandem mass spectrometry (MS/MS) identifies suspected patients with MMA by elevated propionylcarnitine. In addition, a liquid chromatography tandem mass spectrometry (LC/MS/MS) method using dried blood spot is effective to detect some metabolites as a second-tier test, and reduces the false-positive rate in NBS. However, these tests were only used in screening, and not applied as an examination for evaluating treatment. Herein, we describe a 57-day-old girl with MMA under treatment with cobalamin who had elevated urinary methylmalonic acid levels. We applied the LC/MS/MS method with a separation column to evaluate her cobalamin responsiveness, and discovered an insufficient cobalamin dose earlier than would have been possible using other methods. Based on the current data, this method seems to be applicable for the follow-up of the treatment of MMA patients. However, this should be confirmed with more experience with a larger number of cases and a wider spectrum of disorders.
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来源期刊
CiteScore
0.60
自引率
0.00%
发文量
7
审稿时长
12 weeks
期刊介绍: The Journal of Inborn Errors of Metabolism and Screening (JIEMS) is an online peer-reviewed open access journal devoted to publishing clinical and experimental research in inherited metabolic disorders and screening, for health professionals and scientists. Original research articles published in JIEMS range from basic findings that have implications for disease pathogenesis and therapy, passing through diagnosis and screening of metabolic diseases and genetic conditions, and therapy development and outcomes as well. Original articles, reviews on specific topics, brief communications and case reports are welcome. JIEMS aims to become a key resource for geneticists, genetic counselors, biochemists, molecular biologists, reproductive medicine researchers, obstetricians/gynecologists, neonatologists, pediatricians, pathologists and other health professionals interested in inborn errors of metabolism and screening.
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