Translational Metabolic Laboratory, Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
Methods Mol Biol. 2025;2855:555-571. doi: 10.1007/978-1-0716-4116-3_30.
Inborn errors of metabolism constitute a set of hereditary diseases that impose severe medical and physical challenges in the affected individual, in particular, for the pediatric patient population. Timely diagnosis is crucial for these patients, as any delay could result in irreversible health damage, underscoring the importance of early initiation of personalized treatment. Current routine diagnostic screening for inborn errors of metabolism relies on various targeted analyses of established biomarkers. However, this approach is time-consuming, focuses on a limited number of tests (based on clinical information) with a relatively small number of biomarkers, and does not facilitate the identification of new markers. In contrast, untargeted metabolomics-based screening offers a more efficient diagnostic solution, by assessing thousands of metabolites across multiple metabolic pathways in a single test. This not only saves time but also conserves resources for clinicians, the diagnostic laboratory, and for patients.This chapter describes the computational workflow of our "Next Generation Metabolic Screening" approach, which is a metabolomics-based method that is currently applied at the Translational Metabolic Laboratory of the Radboud University Medical Center (the Netherlands) for the diagnosis of inborn errors of metabolism.
先天性代谢缺陷构成了一组遗传性疾病,这些疾病会给受影响的个体带来严重的医疗和身体挑战,特别是儿科患者群体。对于这些患者来说,及时诊断至关重要,因为任何延误都可能导致不可逆转的健康损害,这凸显了尽早开始个性化治疗的重要性。目前,先天性代谢缺陷的常规诊断筛查依赖于对既定生物标志物的各种靶向分析。然而,这种方法既耗时,又只能针对相对较少数量的生物标志物进行有限数量的测试(基于临床信息),并且无法识别新的标志物。相比之下,基于非靶向代谢组学的筛查通过在单次测试中评估多个代谢途径中的数千种代谢物,提供了一种更有效的诊断解决方案。这不仅节省了时间,而且为临床医生、诊断实验室和患者节省了资源。本章描述了我们的“下一代代谢筛查”方法的计算工作流程,这是一种基于代谢组学的方法,目前在 Radboud 大学医学中心(荷兰)的转化代谢实验室中应用于先天性代谢缺陷的诊断。