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二氢硫辛酰胺脱氢酶缺乏症的新生儿筛查:瓜氨酸作为一种有用的分析物。

Newborn screening for dihydrolipoamide dehydrogenase deficiency: Citrulline as a useful analyte.

作者信息

Quinonez Shane C, Seeley Andrea H, Seeterlin Mary, Stanley Eleanor, Ahmad Ayesha

机构信息

University of Michigan, Department of Pediatrics, Division of Pediatric Genetics, 1500 East Medical Center Drive, D5240 MPB/Box 5718, Ann Arbor, MI 48109-5718, USA.

Newborn Screening Section, Michigan Department of Community Health, Bureau of Laboratories, Chemistry and Toxicology, 3350 N. MLK Jr. Blvd., Lansing, MI 48906, USA.

出版信息

Mol Genet Metab Rep. 2014 Aug 15;1:345-349. doi: 10.1016/j.ymgmr.2014.07.007. eCollection 2014.

Abstract

Dihydrolipoamide dehydrogenase deficiency, also known as maple syrup urine disease (MSUD) type III, is caused by the deficiency of the E3 subunit of branched chain alpha-ketoacid dehydrogenase (BCKDH), α-ketoglutarate dehydrogenase (αKGDH), and pyruvate dehydrogenase (PDH). DLD deficiency variably presents with either a severe neonatal encephalopathic phenotype or a primarily hepatic phenotype. As a variant form of MSUD, it is considered a core condition recommended for newborn screening. The detection of variant MSUD forms has proven difficult in the past with no asymptomatic DLD deficiency patients identified by current newborn screening strategies. Citrulline has recently been identified as an elevated dried blood spot (DBS) metabolite in symptomatic patients affected with DLD deficiency. Here we report the retrospective DBS analysis and second-tier allo-isoleucine testing of 2 DLD deficiency patients. We show that an elevated citrulline and an elevated allo-isoleucine on second-tier testing can be used to successfully detect DLD deficiency. We additionally recommend that DLD deficiency be included in the "citrullinemia/elevated citrulline" ACMG Act Sheet and Algorithm.

摘要

二氢硫辛酰胺脱氢酶缺乏症,也称为枫糖尿症(MSUD)III型,是由支链α-酮酸脱氢酶(BCKDH)、α-酮戊二酸脱氢酶(αKGDH)和丙酮酸脱氢酶(PDH)的E3亚基缺乏引起的。DLD缺乏症表现为严重的新生儿脑病表型或主要为肝脏表型。作为MSUD的一种变异形式,它被认为是新生儿筛查推荐的核心疾病。过去,检测MSUD变异形式一直很困难,目前的新生儿筛查策略尚未发现无症状的DLD缺乏症患者。最近发现,在患有DLD缺乏症的有症状患者中,瓜氨酸是干血斑(DBS)中升高的代谢物。在此,我们报告了对2例DLD缺乏症患者的回顾性DBS分析和二线别异亮氨酸检测。我们表明,二线检测中瓜氨酸升高和别异亮氨酸升高可用于成功检测DLD缺乏症。我们还建议将DLD缺乏症纳入“瓜氨酸血症/瓜氨酸升高”ACMG行动清单和算法中。

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引用本文的文献

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本文引用的文献

1
Elevated plasma citrulline: look for dihydrolipoamide dehydrogenase deficiency.
Eur J Pediatr. 2014 Feb;173(2):243-5. doi: 10.1007/s00431-013-2153-x. Epub 2013 Aug 31.
2
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Maple syrup urine disease: further evidence that newborn screening may fail to identify variant forms.
Mol Genet Metab. 2010 Jun;100(2):136-42. doi: 10.1016/j.ymgme.2009.11.010. Epub 2009 Dec 5.
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Newborn screening may fail to identify intermediate forms of maple syrup urine disease.
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