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明尼苏达州新生儿肾上腺脑白质营养不良筛查的见解:5年更新

Insights From Minnesota on Newborn Screening for Adrenoleukodystrophy: A 5-Year Update.

作者信息

Rayannavar Arpana, Billington Charles J, Tryon Rebecca, Kaye Tory, Gupta Ashish, Lund Troy C, Lteif Aida, Adriatico Katherine, Orchard Paul J, Miller Bradley S, Pillai Nishitha R

机构信息

Division of Pediatric Endocrinology, Department of Pediatrics, University of Minnesota, Minneapolis, Minnesota, USA.

M Health Fairview Masonic Children's Hospital, Minneapolis, Minnesota, USA.

出版信息

Am J Med Genet A. 2025 May;197(5):e63995. doi: 10.1002/ajmg.a.63995. Epub 2025 Jan 13.

Abstract

Our objectives are to report on the outcomes of adrenal insufficiency (AI) and cerebral ALD (cALD) in children diagnosed with X-linked adrenoleukodystrophy (ALD) identified by newborn screening (NBS) in Minnesota in the first 5 years following initiation of NBS in 02/2017. A retrospective chart review was conducted for children diagnosed with ALD via Minnesota NBS from 02/06/2017 through 02/06/2022. Data reviewed included newborn screening data, diagnostic very long chain fatty acid levels, ABCD1 molecular testing results, serial measurements of ACTH and cortisol, and serial brain MRI results. Thirty-two boys and 11 girls were molecularly and/or biochemically confirmed to have ALD. Of these 32 boys, six (2-7 years; median age:18 months) developed AI. Two boys developed cALD and underwent stem cell transplantation, one of whom also has been diagnosed with AI. All the pathogenic/likely pathogenic variants detected during the first 5 years had initial C26:0 lysophosphatidylcholine (C26:0 lysoPC) values over 0.3 μmol/L at the time of newborn screening. The addition of ALD to NBS in Minnesota has allowed for early detection of asymptomatic AI in six young patients and asymptomatic cALD in two patients. Data from our study shows a positive correlation between high newborn screening LysoPC levels and variant pathogenicity.

摘要

我们的目标是报告2017年2月明尼苏达州开展新生儿筛查(NBS)后的头5年中,通过NBS确诊为X连锁肾上腺脑白质营养不良(ALD)的儿童的肾上腺功能不全(AI)和脑型ALD(cALD)的结局。对2017年6月2日至2022年6月2日期间通过明尼苏达州NBS确诊为ALD的儿童进行了回顾性病历审查。审查的数据包括新生儿筛查数据、诊断性极长链脂肪酸水平、ABCD1分子检测结果、促肾上腺皮质激素(ACTH)和皮质醇的系列测量结果以及系列脑部磁共振成像(MRI)结果。32名男孩和11名女孩经分子和/或生化确诊患有ALD。在这32名男孩中,6名(2至7岁;中位年龄:18个月)出现了AI。2名男孩患上了cALD并接受了干细胞移植,其中1名也被诊断出患有AI。在头5年中检测到的所有致病/可能致病变异在新生儿筛查时的初始C26:0溶血磷脂酰胆碱(C26:0 lysoPC)值均超过0.3μmol/L。明尼苏达州将ALD纳入NBS后,得以早期发现6名年轻患者的无症状AI和2名患者的无症状cALD。我们的研究数据显示,新生儿筛查LysoPC水平高与变异致病性之间存在正相关。

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