lunes, 18 de marzo de 2013

Identification of Infants at Risk for Developing F... [J Pediatr. 2013] - PubMed - NCBI

Identification of Infants at Risk for Developing F... [J Pediatr. 2013] - PubMed - NCBI


2013 Mar 1. pii: S0022-3476(13)00065-6. doi: 10.1016/j.jpeds.2013.01.031. [Epub ahead of print]


Identification of Infants at Risk for Developing Fabry, Pompe, or Mucopolysaccharidosis-I from Newborn Blood Spots by Tandem Mass Spectrometry.





Source


Department of Pediatrics, University of Washington, Seattle, WA. Electronic address: crscott@u.washington.edu.



Abstract




OBJECTIVE:


To assess the performance of a tandem mass spectrometry (MS/MS) technology in a newborn screening laboratory to simultaneously measure α-galactosidase, acid-α-glucosidase, and α-L-iduronidase for the detection of infants at risk to develop Fabry, Pompe, or mucopolysaccharidosis (MPS)-I diseases.


STUDY DESIGN:


Enzyme activity was assayed from a 3.2-mm punch from 100 000+ anonymous newborn blood spots. Punches with low enzyme activity were further evaluated by nucleotide sequence analysis of the responsible gene. Confirmation of affected infants was dependent on identification of mutations compatible with diminished enzyme activity.


RESULTS:


The technology for simultaneously measuring multiple enzyme activities by MS/MS was successful. The confirmation of diagnosis for Fabry, Pompe, or MPS-I, by DNA sequencing estimated the prevalence of Fabry disease at 1/7800 males (95% CI 1/17 800-1/3600); Pompe disease at 1/27 800 newborns (95% CI 1/90 000-1/10 200); and MPS-I at 1/35 500 newborns (95% CI 1/143 000-1/11 100). These estimates of prevalence are 2 to 4 times greater than the prevalence estimated by clinical diagnosis. The combined prevalence for the 3 disorders was 1/7500 newborns (95% CI 1/13 500-1/4500).


CONCLUSIONS:


MS/MS for the simultaneous assay of multiple lysosomal enzymes can be successfully introduced into a routine newborn screening laboratory. The technology has a positive predictive value equal to, or better, than methods currently used for the detection of nonlysosomal disorders. Using newborn blood spots, the combined prevalence of Fabry, Pompe, and MPS-I is estimated at 1/7500 newborns based on low-enzyme activity and confirmation by mutation analysis.
Copyright © 2013 Mosby, Inc. All rights reserved.






PMID:

23465405
[PubMed - as supplied by publisher]



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