Abstract

Started in 1963 by Robert Guthrie, newborn screening (NBS) is considered to be one of the great public health achievements. Its original goal was to screen newborns for conditions that could benefit from presymptomatic treatment, thereby reducing associated morbidity and mortality. With advances in technology, the number of disorders included in NBS programs increased. Pompe disease is a good candidate for NBS. Because decisions regarding which diseases should be included in NBS panels are made regionally and locally, programs and efforts for NBS for Pompe disease have been inconsistent both in the United States and globally. In this article, published in the "Newborn Screening, Diagnosis, and Treatment for Pompe Disease" guidance supplement, the Pompe Disease Newborn Screening Working Group, an international group of experts in both NBS and Pompe disease, review the methods used for NBS for Pompe disease and summarize results of current and ongoing NBS programs in the United States and other countries. Challenges and potential drawbacks associated with NBS also are discussed.

Highlights

  • The effectiveness of newborn screening Recommended Uniform Screening Panel (RUSP) (NBS) in LSDs to improve outcomes was first demonstrated in Pompe disease

  • Results of NBS have been summarized for 473 738 newborn samples screened for Pompe disease

  • Two assays were performed at screening: acid α-glucosidase infantile-onset Pompe disease (IOPD) (GAA) activity measured at pH 3.8 in the presence of acarbose and neutral α-glucosidase (NAG) activity measured at pH 7.0 without acarbose

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Summary

Newborn Screening for Pompe Disease

Ronald Scott, MD,b Roberto Giugliani, MD, PhD,c on behalf of the Pompe Disease Newborn Screening Working Group abstract. Started in 1963 by Robert Guthrie, newborn screening (NBS) is considered to be one of the great public health achievements. Because decisions regarding which diseases should be included in NBS panels are made regionally and locally, programs and efforts for NBS for Pompe disease have been inconsistent both in the United States and globally. In this article, published in the “Newborn Screening, Diagnosis, and Treatment for Pompe Disease” guidance supplement, the Pompe Disease Newborn Screening Working Group, an international group of experts in both NBS and Pompe disease, review the methods used for NBS for Pompe disease and summarize results of current and ongoing NBS programs in the United States and other countries. The guidelines/recommendations in this article are not American Academy of Pediatrics policy, and publication does not imply endorsement. 2017; 140(s1):e20160280C

NEWBORN SCREENING
NBS AND POMPE DISEASE
FOR NBS FOR POMPE DISEASE
Yes Yes Yes Yes Missouri
New Yorkd
MOLECULAR SEQUENCING
PSEUDODEFICIENCY IN POMPE DISEASE AND ITS EFFECT IN NBS
SUMMARY OF RESULTS OF NBS PROGRAMS FOR POMPE DISEASE
Global NBS Initiatives
NBS Programs in the United States
New York
Full Text
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