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Cited by 677

The DOI matches its Crossref record; 15 of the 15 references it cites were found in a registry or an index.

Screening Newborns for Inborn Errors of Metabolism by Tandem Mass Spectrometry

Wilcken, Bridget, Wiley, Veronica, Hammond, Judith, Carpenter, Kevin·2003·New England Journal of Medicine

Abstract

BACKGROUND: The recent development of electrospray tandem mass spectrometry makes it possible to screen newborns for many rare inborn errors of metabolism, but the efficacy and outcomes of screening remain unknown. We examined the effect of the screening of newborns by tandem mass spectrometry on the rates of diagnosis of 31 disorders. METHODS: We compared the rates of detection of 31 inborn errors affecting the metabolism of the urea cycle, amino acids, and organic acids and fatty-acid oxidation among 362,000 newborns screened by tandem mass spectrometry over a four-year period (April 1998 through March 2002) with the rates in six preceding four-year birth cohorts in New South Wales and the Australian Capital Territory, Australia, where screening, diagnostic, and clinical services were centralized. RESULTS: The overall prevalence of disorders during the periods when clinical diagnosis was used did not vary between 1982 and 1998. In the cohort screened with tandem mass spectrometry, the prevalence of inborn errors, excluding phenylketonuria, was 15.7 per 100,000 births (95 percent confidence interval, 11.9 to 20.4), as compared with adjusted rates of 8.6 to 9.5 per 100,000 births in the four preceding four-year cohorts. Of the 57 cases diagnosed after the introduction of newborn screening, 15 were diagnosed clinically; 7 of the 15 newborns had a normal result on screening. The rate of detection was increased specifically for medium-chain acyl-coenzyme A dehydrogenase deficiency (P<0.001) and other disorders of fatty-acid oxidation (P=0.007), as compared with the 16-year period before the implementation of neonatal screening for these disorders. CONCLUSIONS: More cases of inborn errors of metabolism are diagnosed by screening with tandem mass spectrometry than are diagnosed clinically. It is not yet clear which patients with disorders diagnosed by such screening would have become symptomatic if screening had not been performed.

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Metadata

Authors
Wilcken, B., Wiley, V., Hammond, J., & Carpenter, K.
Venue
New England Journal of Medicine
Published
2003-06-05
Volume
348
Issue
23
Pages
2304-2312
ISSN
  • 0028-4793 (ISSN-L)
  • 1533-4406
OpenAlex
W2004235323
Cited by
677
References
15
FWCI
21.30
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Screening Newborns for Inborn Errors of Metabolism by Tandem Mass Spectrometry. https://app.cochat.ai/papers/10.1056/nejmoa025225
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Wilcken, B., Wiley, V., Hammond, J., & Carpenter, K. (2003). Screening Newborns for Inborn Errors of Metabolism by Tandem Mass Spectrometry. New England Journal of Medicine. https://doi.org/10.1056/nejmoa025225

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.