Newborn screening for the full set of mucopolysaccharidoses in dried blood spots based on first-tier enzymatic assay followed by second-tier analysis of glycosaminoglycans

Mol Genet Metab. 2023 Nov;140(3):107698. doi: 10.1016/j.ymgme.2023.107698. Epub 2023 Sep 7.

Abstract

Newborn screening (NBS) for the full set of mucopolysaccharidoses (MPSs) is now possible by either measuring all of the relevant enzymatic activities in dried blood spots (DBS) using tandem mass spectrometry followed by measurement of accumulated glycosaminoglycans (GAGs) or the vice-versa approach. In this study we considered multiple factors in detail including reagent costs, time per analysis, false positive rates, instrumentation requirements, and multiplexing capability. Both NBS approaches are found to provide acceptable solutions for comprehensive MPS NBS, but the enzyme-first approach allows for better multiplexing to include numerous additional diseases that are appropriate for NBS expansion. By using a two-tier NBS approach, the false positive and false negatives rates are expected to acceptably low and close to zero.

Keywords: Biochemical genetics; Inborn errors of metabolism; Lysosomal storage diseases; Newborn screening; Tandem mass spectrometry.

Publication types

  • Review
  • Research Support, N.I.H., Extramural

MeSH terms

  • Enzyme Assays
  • Glycosaminoglycans*
  • Humans
  • Infant, Newborn
  • Mucopolysaccharidoses*
  • Neonatal Screening / methods
  • Tandem Mass Spectrometry / methods

Substances

  • Glycosaminoglycans