Clinical outcomes of children with abnormal newborn screening results for Krabbe disease in New York State.

Published

Journal Article

BACKGROUND: Early infantile Krabbe disease is rapidly fatal, but hematopoietic stem cell transplantation (HSCT) may improve outcomes if performed soon after birth. New York State began screening all newborns for Krabbe disease in 2006. METHODS: Infants with abnormal newborn screen results for Krabbe disease were referred to specialty-care centers. Newborns found to be at high risk for Krabbe disease underwent a neurodiagnostic battery to determine the need for emergent HSCT. RESULTS: Almost 2 million infants were screened. Five infants were diagnosed with early infantile Krabbe disease. Three died, two from HSCT-related complications and one from untreated disease. Two children who received HSCT have moderate to severe developmental delays. Forty-six currently asymptomatic children are considered to be at moderate or high risk for development of later-onset Krabbe disease. CONCLUSIONS: These results show significant HSCT-associated morbidity and mortality in early infantile Krabbe disease and raise questions about its efficacy when performed in newborns diagnosed through newborn screening. The unanticipated identification of "at risk" children introduces unique ethical and medicolegal issues. New York's experience raises questions about the risks, benefits, and practicality of screening newborns for Krabbe disease. It is imperative that objective assessments be made on an ongoing basis as additional states begin screening for this disorder.Genet Med 18 12, 1235-1243.

Full Text

Duke Authors

Cited Authors

  • Wasserstein, MP; Andriola, M; Arnold, G; Aron, A; Duffner, P; Erbe, RW; Escolar, ML; Estrella, L; Galvin-Parton, P; Iglesias, A; Kay, DM; Kronn, DF; Kurtzberg, J; Kwon, JM; Langan, TJ; Levy, PA; Naidich, TP; Orsini, JJ; Pellegrino, JE; Provenzale, JM; Wenger, DA; Caggana, M

Published Date

  • December 2016

Published In

Volume / Issue

  • 18 / 12

Start / End Page

  • 1235 - 1243

PubMed ID

  • 27171547

Pubmed Central ID

  • 27171547

Electronic International Standard Serial Number (EISSN)

  • 1530-0366

Digital Object Identifier (DOI)

  • 10.1038/gim.2016.35

Language

  • eng

Conference Location

  • United States