The new frontier of newborn screening: integrating genomics, metabolomics, and data science for inborn errors of metabolism.

IF 3.6 2区 医学 Q2 GENETICS & HEREDITY
Muhammad Wasim, Yajun Wang, Guoda Ma
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引用次数: 0

Abstract

Newborn screening (NBS) for inborn errors of metabolism (IEMs) represents one of the most successful public health initiatives of the past century. Originating with the simple bacterial inhibition assay for phenylketonuria, the field was revolutionized by tandem mass spectrometry (MS/MS). Today, we stand at the precipice of a second, more profound revolution driven by the convergence of high-throughput genomics, next-generation metabolomics, and advanced data science. This review articulates this paradigm shift, detailing how MS/MS is being augmented by targeted DNA analysis and how whole genome sequencing and untargeted metabolomics, integrated with artificial intelligence, are expanding the detectable universe of disorders and enabling precision interventions. However, this powerful multi-omic approach raises critical challenges: incomplete penetrance, overdiagnosis, economic burden, psychosocial impacts, algorithm biases, and the genomic data gap that exacerbates health disparities. We critically examine the practical limitations of AI, the lack of evidence for cost-effectiveness, the slow pace of database updates, and the need for short-term reanalysis systems to "rescue" cases left undiagnosed. Global policy variations and data-sharing governance frameworks are also addressed. We conclude that the future of NBS lies not in sequential technology replacement, but in the responsible creation of a sophisticated, multi-omic biomedical information system to transform NBS into a foundational pillar of precision pediatric medicine.

新生儿筛查的新前沿:整合基因组学,代谢组学和数据科学的先天性代谢错误。
新生儿筛查(NBS)先天性代谢错误(IEMs)是上个世纪最成功的公共卫生举措之一。起源于苯丙酮尿的简单细菌抑制试验,串联质谱(MS/MS)彻底改变了这一领域。今天,在高通量基因组学、下一代代谢组学和先进数据科学的融合推动下,我们正站在第二次更深刻的革命的边缘。这篇综述阐述了这种范式转变,详细介绍了靶向DNA分析如何增强质谱/质谱,以及全基因组测序和非靶向代谢组学如何与人工智能相结合,扩大了可检测的疾病范围,并实现了精确干预。然而,这种强大的多组学方法提出了严峻的挑战:不完全外显率、过度诊断、经济负担、社会心理影响、算法偏差以及加剧健康差距的基因组数据差距。我们严格审查了人工智能的实际局限性,缺乏成本效益证据,数据库更新速度缓慢,以及需要短期再分析系统来“拯救”未诊断的病例。还讨论了全球政策变化和数据共享治理框架。我们得出结论,NBS的未来不在于连续的技术替代,而在于负责任地创建一个复杂的多基因组生物医学信息系统,使NBS成为精准儿科医学的基础支柱。
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来源期刊
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases 医学-医学:研究与实验
CiteScore
6.30
自引率
8.10%
发文量
418
审稿时长
4-8 weeks
期刊介绍: Orphanet Journal of Rare Diseases is an open access, peer-reviewed journal that encompasses all aspects of rare diseases and orphan drugs. The journal publishes high-quality reviews on specific rare diseases. In addition, the journal may consider articles on clinical trial outcome reports, either positive or negative, and articles on public health issues in the field of rare diseases and orphan drugs. The journal does not accept case reports.
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