Matern Dietrich, Basheeruddin Khaja, Klug Tracy L, McKee Gwendolyn, Edge Patricia U, Hall Patricia L, Kurtzberg Joanne, Orsini Joseph J
Biochemical Genetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Illinois Department of Public Health, Chicago, IL 60612, USA.
Int J Neonatal Screen. 2024 Jan 28;10(1):10. doi: 10.3390/ijns10010010.
Krabbe disease (KD) is part of newborn screening (NBS) in 11 states with at least one additional state preparing to screen. In July 2021, KD was re-nominated for addition to the federal Recommended Uniform Screening Panel (RUSP) in the USA with a two-tiered strategy based on psychosine (PSY) as the determinant if an NBS result is positive or negative after a first-tier test revealed decreased galactocerebrosidase activity. Nine states currently screening for KD include PSY analysis in their screening strategy. However, the nomination was rejected in February 2023 because of perceived concerns about a high false positive rate, potential harm to newborns with an uncertain prognosis, and inadequate data on presymptomatic treatment benefit or harm. To address the concern about false positive NBS results, a survey was conducted of the eight NBS programs that use PSY and have been screening for KD for at least 1 year. Seven of eight states responded. We found that: (1) the use of PSY is variable; (2) when modeling the data based on the recommended screening strategy for KD, and applying different cutoffs for PSY, each state could virtually eliminate false positive results without major impact on sensitivity; (3) the reason for the diverse strategies appears to be primarily the difficulty of state programs to adjust screening algorithms due to the concern of possibly missing even an adult-onset case following a change that focuses on infantile and early infantile KD. Contracts with outside vendors and the effort/cost of making changes to a program's information systems can be additional obstacles. We recommend that programs review their historical NBS outcomes for KD with their advisory committees and make transparent decisions on whether to accept false positive results for such a devastating condition or to adjust their procedures to ensure an efficient, effective, and manageable NBS program for KD.
克拉伯病(KD)是11个州新生儿筛查(NBS)的一部分,还有至少一个州正准备开展筛查。2021年7月,KD被重新提名加入美国联邦推荐统一筛查小组(RUSP),采用基于鞘氨醇(PSY)的两层策略,即在一级检测显示半乳糖脑苷脂酶活性降低后,根据PSY来判定NBS结果为阳性或阴性。目前有9个州对KD进行筛查,其筛查策略中包括PSY分析。然而,由于担心假阳性率高、对预后不确定的新生儿可能造成伤害以及缺乏症状前治疗益处或危害的充分数据,该提名在2023年2月被否决。为了解决对NBS假阳性结果的担忧,对8个使用PSY且已对KD进行至少1年筛查的NBS项目进行了一项调查。8个州中有7个做出了回应。我们发现:(1)PSY的使用情况各不相同;(2)在根据推荐的KD筛查策略对数据进行建模,并应用不同的PSY临界值时,每个州几乎都可以消除假阳性结果,而不会对敏感性产生重大影响;(3)策略多样的原因似乎主要是各州项目难以调整筛查算法,因为担心在专注于婴儿型和早发型KD的改变之后,甚至可能漏诊成人发病的病例。与外部供应商的合同以及对项目信息系统进行更改的工作量/成本可能是额外的障碍。我们建议各项目与其咨询委员会一起审查其KD的历史NBS结果,并就是否接受这种毁灭性疾病的假阳性结果或调整其程序以确保KD的NBS项目高效、有效且可管理做出透明的决定。