Newborn Screening for Krabbe Disease: Status Quo and Recommendations for Improvements

被引:2
作者
Matern, Dietrich [1 ]
Basheeruddin, Khaja [2 ]
Klug, Tracy L. [3 ]
McKee, Gwendolyn [4 ]
Edge, Patricia U. [5 ]
Hall, Patricia L. [1 ]
Kurtzberg, Joanne [6 ]
Orsini, Joseph J. [7 ]
机构
[1] Dept Lab Med & Pathol, Mayo Clin, Biochem Genet Lab, Rochester, MN 55905 USA
[2] Illinois Dept Publ Hlth, Chicago, IL 60612 USA
[3] Missouri State Publ Hlth Lab, Jefferson City, MO 65101 USA
[4] Tennessee Dept Hlth, Div Lab Serv, Nashville, TN 37243 USA
[5] Penn Dept Hlth, Harrisburg, PA 17120 USA
[6] Duke Univ, Med Ctr, Dept Pediat, Durham, NC 27705 USA
[7] Wadsworth Ctr, New York State Dept Hlth, Newborn Screening Program, Albany, NY 12208 USA
关键词
Krabbe disease; newborn screening; globoid cell leukodystrophy; galactocerebrosidase; psychosine; false positive rate; hematopoietic stem cell transplant; DRIED BLOOD SPOTS; PSYCHOSINE;
D O I
10.3390/ijns10010010
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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.
引用
收藏
页数:9
相关论文
共 25 条
[1]   Precision newborn screening for lysosomal disorders [J].
Baerg, Melissa M. Minter ;
Stoway, Stephanie D. ;
Hart, Jeremy ;
Mott, Lea ;
Peck, Dawn S. ;
Nett, Stephanie L. ;
Eckerman, Jason S. ;
Lacey, Jean M. ;
Turgeon, Coleman T. ;
Gavrilov, Dimitar ;
Oglesbee, Devin ;
Raymond, Kimiyo ;
Tortorelli, Silvia ;
Matern, Dietrich ;
Morkrid, Lars ;
Rinaldo, Piero .
GENETICS IN MEDICINE, 2018, 20 (08) :847-854
[2]   A prospective natural history study of Krabbe disease in a patient cohort with onset between 6 months and 3 years of life [J].
Bascou, Nicholas ;
DeRenzo, Anthony ;
Poe, Michele D. ;
Escolar, Maria L. .
ORPHANET JOURNAL OF RARE DISEASES, 2018, 13
[3]   Newborn Screening for Krabbe Disease-Illinois Experience: Role of Psychosine in Diagnosis of the Disease [J].
Basheeruddin, Khaja ;
Shao, Rong ;
Balster, Fran ;
Gardley, Pearlie ;
Ashbaugh, Laura .
INTERNATIONAL JOURNAL OF NEONATAL SCREENING, 2021, 7 (02)
[4]   Determination of psychosine concentration in dried blood spots from newborns that were identified via newborn screening to be at risk for Krabbe disease [J].
Chuang, Wei-Lien ;
Pacheco, Josh ;
Zhang, X. Kate ;
Martin, Monica M. ;
Biski, Chad K. ;
Keutzer, Joan M. ;
Wenger, David A. ;
Caggana, Michele ;
Orsini, Joseph J., Jr. .
CLINICA CHIMICA ACTA, 2013, 419 :73-76
[5]   Low Psychosine in Krabbe Disease with Onset in Late Infancy: A Case Report [J].
Corre, Camille S. ;
Matern, Dietrich ;
Pellegrino, Joan E. ;
Saavedra-Matiz, Carlos A. ;
Orsini, Joseph J. ;
Thompson-Stone, Robert .
INTERNATIONAL JOURNAL OF NEONATAL SCREENING, 2021, 7 (02)
[6]   Transplantation of umbilical-cord blood in babies with infantile Krabbe's disease [J].
Escolar, ML ;
Poe, MD ;
Provenzale, JM ;
Richards, KC ;
Allison, J ;
Wood, S ;
Wenger, DA ;
Pietryga, D ;
Wall, D ;
Champagne, M ;
Morse, R ;
Krivit, W ;
Kurtzberg, J .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 352 (20) :2069-2081
[7]   The critical role of psychosine in screening, diagnosis, and monitoring of Krabbe disease [J].
Guenzel, Adam J. ;
Turgeon, Coleman T. ;
Nickander, Kim K. ;
White, Amy L. ;
Peck, Dawn S. ;
Pino, Gisele B. ;
Studinski, April L. ;
Prasad, Vinod K. ;
Kurtzberg, Joanne ;
Escolar, Maria L. ;
Lasio, Maria Laura Duque ;
Pellegrino, Joan E. ;
Sakonju, Ai ;
Hickey, Rachel E. ;
Shallow, Natalie M. ;
Ream, Margie A. ;
Orsini, Joseph J. ;
Gelb, Michael H. ;
Raymond, Kimiyo ;
Gavrilov, Dimitar K. ;
Oglesbee, Devin ;
Rinaldo, Piero ;
Tortorelli, Silvia ;
Matern, Dietrich .
GENETICS IN MEDICINE, 2020, 22 (06) :1108-1118
[8]   PATHOLOGICAL AND BIOCHEMICAL-STUDIES OF FETAL KRABBE DISEASE [J].
IDA, H ;
RENNERT, OM ;
WATABE, K ;
ETO, Y ;
MAEKAWA, K .
BRAIN & DEVELOPMENT, 1994, 16 (06) :480-484
[9]   Weighing the evidence for newborn screening for early-infantile Krabbe disease [J].
Kemper, Alex R. ;
Knapp, Alixandra A. ;
Green, Nancy S. ;
Comeau, Anne Marie ;
Metterville, Danielle R. ;
Perrin, James M. .
GENETICS IN MEDICINE, 2010, 12 (09) :539-543
[10]   A new familial, infantile form of diffuse brain-sclerosis [J].
Krabbe, K .
BRAIN, 1916, 39 :74-114