Trampuž Domen, Schielen Peter C J I, Zetterström Rolf H, Scarpa Maurizio, Feillet François, Kožich Viktor, Tangeraas Trine, Drole Torkar Ana, Mlinarič Matej, Perko Daša, Remec Žiga Iztok, Lampret Barbka Repič, Battelino Tadej, van Spronsen Francjan J, Bonham James R, Grošelj Urh
Clinical Institute for Special Laboratory Diagnostics, University Children's Hospital, Ljubljana University Medical Center, Vrazov trg 1, 1000 Ljubljana, Slovenia.
International Society for Neonatal Screening, Reigerskamp 273, 3607 HP Stichtse Vecht, The Netherlands.
Int J Neonatal Screen. 2025 Feb 26;11(1):18. doi: 10.3390/ijns11010018.
Newborn screening for Phenylketonuria enables early detection and timely treatment with a phenylalanine-restricted diet to prevent severe neurological impairment. Although effective and in use for 60 years, screening, diagnostic, and treatment practices still vary widely across countries and centers. To evaluate the Phenylketonuria newborn screening practices internationally, we designed a survey with questions focusing on the laboratory aspect of the screening system. We analyzed 24 completed surveys from 23 countries. Most participants used the same sampling age range of 48-72 h; they used tandem mass spectrometry and commercial non-derivatized kits to measure phenylalanine (Phe), and had non-negative cut-off values (COV) set mostly at 120 µmol/L of Phe. Participants mostly used genetic analysis of blood and detailed amino acid analysis from blood plasma as their confirmatory methods and set the COV for the initiation of dietary therapy at 360 µmol/L of Phe. There were striking differences in practice as well. While most participants reported a 48-72 h range for age at sampling, that range was overall quite diverse Screening COV varied as well. Additional screening parameters, e.g., the phenylalanine/tyrosine ratio were used by some participants to determine the screening result. Some participants included testing for tetrahydrobiopterin deficiency, or galactosemia in their diagnostic process. Results together showed that there is room to select a best practice from the many practices applied. Such a best practice of PKU-NBS parameters and post-screening parameters could then serve as a generally applicable guideline.
苯丙酮尿症新生儿筛查能够实现早期检测,并通过限制苯丙氨酸饮食进行及时治疗,以预防严重的神经损伤。尽管该筛查方法有效且已使用60年,但各国和各中心的筛查、诊断及治疗方法仍存在很大差异。为了评估国际上苯丙酮尿症新生儿筛查的实践情况,我们设计了一项调查,问题聚焦于筛查系统的实验室方面。我们分析了来自23个国家的24份完整调查问卷。大多数参与者采用相同的48 - 72小时采样年龄范围;他们使用串联质谱法和商业非衍生化试剂盒来测量苯丙氨酸(Phe),且非负临界值(COV)大多设定为120 μmol/L的苯丙氨酸。参与者大多采用血液基因分析和血浆详细氨基酸分析作为确诊方法,并将饮食治疗起始的临界值设定为360 μmol/L的苯丙氨酸。实践中也存在显著差异。虽然大多数参与者报告采样年龄范围为48 - 72小时,但该范围总体差异较大。筛查临界值也各不相同。一些参与者使用其他筛查参数,例如苯丙氨酸/酪氨酸比值来确定筛查结果。一些参与者在诊断过程中包括对四氢生物蝶呤缺乏症或半乳糖血症的检测。结果共同表明,在众多应用的方法中仍有选择最佳实践的空间。这样一种苯丙酮尿症新生儿筛查参数及筛查后参数的最佳实践随后可作为普遍适用的指南。