Langeveld Mirjam, Sirrs Sandra, Schoenmakers Daphne H, Fazio Timothy, van der Klauw Melanie M, Maillot Francois, Sharma Reena, Tran Christel, Ziagaki Athanasia, Mochel Fanny
Department of Endocrinology and Metabolism and Amsterdam Gastroenterology Endocrinology and Metabolism Research Institute, Amsterdam University Medical Centers, Amsterdam, the Netherlands.
Department of Medicine, Division of Endocrinology, University of British Columbia, Vancouver, British Columbia, Canada.
J Inherit Metab Dis. 2025 Jul;48(4):e70057. doi: 10.1002/jimd.70057.
The number of inherited metabolic diseases (IMDs) in newborn screening (NBS) programs has increased significantly in the past decades. For some of the IMDs included in NBS (e.g., tyrosinemia type I), there are clear and substantial health benefits of NBS, while for others (e.g., very long chain acyl CoA dehydrogenase deficiency and 3-methylcrotonyl CoA carboxylase 1 deficiency), this is less clear as NBS identifies individuals who are asymptomatic or have milder forms of the disease. Therefore, knowledge of the full disease spectrum (including later onset forms) is needed when setting diagnostic metabolite cut-offs for NBS. Insights into the clinical, genetic and biochemical characteristics of different patient subsets can be used to redefine NBS protocols to identify patients with more severe forms of the disease who are most likely to benefit from identification in the newborn period. These insights require life-long monitoring of individuals identified based on symptoms versus those identified by NBS to determine long-term health outcomes and quantify the benefits of NBS. Adult metabolic specialists should be included in the development of NBS programs to provide data from this long-term monitoring and to contribute specific knowledge about later onset phenotypes of the IMDs included in NBS programs. The goal should be to develop NBS programs that identify newborns that benefit from early disease detection and treatment, without increasing psychological, social and management burden for individuals who may develop disease in adulthood with milder phenotype or potentially even not at all.
在过去几十年中,新生儿筛查(NBS)项目中遗传性代谢疾病(IMD)的数量显著增加。对于NBS所涵盖的一些IMD(例如I型酪氨酸血症),NBS具有明确且显著的健康益处,而对于其他一些疾病(例如极长链酰基辅酶A脱氢酶缺乏症和3 - 甲基巴豆酰辅酶A羧化酶1缺乏症),情况则不太明确,因为NBS所识别的个体无症状或患有症状较轻的疾病形式。因此,在为NBS设定诊断代谢物临界值时,需要了解完整的疾病谱(包括迟发型形式)。对不同患者亚组的临床、遗传和生化特征的深入了解可用于重新定义NBS方案,以识别患有更严重疾病形式的患者,这些患者最有可能从新生儿期的识别中受益。这些深入了解需要对基于症状识别的个体与通过NBS识别的个体进行终身监测,以确定长期健康结果并量化NBS的益处。在NBS项目的开发过程中应纳入成人代谢专家,以提供来自这种长期监测的数据,并贡献有关NBS项目中所包含的IMD迟发型表型的特定知识。目标应该是开发NBS项目,识别出能从早期疾病检测和治疗中受益的新生儿,同时又不增加那些成年后可能出现较轻表型疾病甚至可能根本不发病的个体的心理负担以及社会和管理负担。