新生儿VLCADD筛查综述:威斯康星州的经验。

IF 4 Q1 GENETICS & HEREDITY
Breanna Mitchell, Jessica Scott-Schwoerer, Ashley Kuhl, Kristina Garcia, Patrice Held
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引用次数: 0

摘要

超长链酰基辅酶a脱氢酶缺乏症(VLCADD)是由于长链脂肪酸代谢缺陷引起的。患有VLCADD的婴儿可能会出现心肌病、低血糖,甚至死亡;因此,早期发现和干预至关重要。然而,疾病谱和新生儿代谢的自然变化导致患病个体和未患病个体之间酰基肉碱值重叠,这导致难以识别真阳性病例,同时最大限度地减少假阳性病例。2000年,VLCADD被添加到威斯康星州的新生儿筛查(NBS)小组中。之前对2000年至2014年期间发现的VLCADD筛查阳性病例进行的回顾性审查导致筛查算法发生变化。实施后,在2015年至2021年期间,假阳性筛查比例从25.3%降至20.4%。由于确定的携带者数量增加(2000-2014年占病例的27.5%,2015-2021年占病例的51.8%),总体PPV也从37.2%下降到28%。数据回顾还发现了三种长链酰基肉碱浓度(C14:1、C14:1/C16和C14:1/C2)在真阳性人群和假阳性人群中具有统计学显著差异。在新生儿筛查中使用C14:1、C14:1/C16和C14:1/C2值可以更清楚地区分真阳性和携带人群,并增加该筛查的PPV。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Review of Newborn Screening for VLCADD: The Wisconsin Experience.

Very-long-chain acyl-CoA dehydrogenase deficiency (VLCADD) is due to a defect in metabolism of long-chain fatty acids. Infants with VLCADD may experience cardiomyopathy, hypoglycemia, or even death; thus, early detection and intervention is crucial. The spectrum of disease and natural variation in newborn metabolism, however, lead to overlap in acylcarnitine values between affected and unaffected individuals, which contributes to the difficulty in identifying true positive cases while minimizing false positive cases. VLCADD was added to the state of Wisconsin's newborn screening (NBS) panel in 2000. A previous retrospective review of VLCADD screen positive cases identified between 2000 and 2014 resulted in a change to the screening algorithm. Following implementation, a reduction in the percentage of false positive screens from 25.3% to 20.4% was observed between 2015 and 2021. The overall PPV also decreased, from 37.2% to 28%, due to an increase in the number of carriers identified (27.5% of cases in 2000-2014 and 51.8% of cases in 2015-2021). A data review also identified three long-chain acylcarnitine elevations (C14:1, C14:1/C16, and C14:1/C2) that had statistically significant differences in concentrations in true positive populations versus false positive populations. Utilization of the C14:1, C14:1/C16, and C14:1/C2 values in newborn screening may provide clearer distinction between true positive and carrier populations and additionally increase the PPV of this screen.

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来源期刊
International Journal of Neonatal Screening
International Journal of Neonatal Screening Medicine-Pediatrics, Perinatology and Child Health
CiteScore
6.70
自引率
20.00%
发文量
56
审稿时长
11 weeks
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