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
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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Farrell, P. M., Kosorok, M. R., Rock, M. J., Laxova, A., Zeng, L., Lai, H.-C., Hoffman, G., Laessig, R. H., Splaingard, M. L., & the Wisconsin Cystic Fibrosis Neonatal Screening Study Group (2001) · Pediatrics · doi:10.1542/peds.107.1.1 · Cited by 837
Zytkovicz, T. H., Fitzgerald, E. F., Marsden, D., Larson, C. A., Shih, V. E., Johnson, D. M., Strauss, A. W., Comeau, A. M., Eaton, R. B., & Grady, G. F. (2001) · Clinical Chemistry · doi:10.1093/clinchem/47.11.1945 · Cited by 505
Medium–chain acyl-coenzyme A dehydrogenase deficiency: Clinical course in 120 affected children
Iafolla, A. K., Thompson, R. J., & Roe, C. R. (1994) · The Journal of Pediatrics · doi:10.1016/s0022-3476(94)70363-9 · Cited by 274
Chatfield, S., Owen, G., Ryley, H. C., Williams, J., Alfaham, M., Goodchild, M. C., & Weller, P. (1991) · Archives of Disease in Childhood · doi:10.1136/adc.66.1_spec_no.29 · Cited by 158
Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia
Wiley, V. C., Carpenter, K. H., & Wilcken, B. M. (1999) · Acta Paediatrica · doi:10.1111/j.1651-2227.1999.tb01157.x · Cited by 131
Self-citationRapid Diagnosis of Methylmalonic and Propionic Acidemias
Chace, D. H., DiPerna, J. C., Kalas, T. A., Johnson, R. W., & Naylor, E. W. (2001) · Clinical Chemistry · doi:10.1093/clinchem/47.11.2040 · Cited by 98
Wilcken, B., Wiley, V. C., Sim, K. G., & Carpenter, K. H. (2001) · The Journal of Pediatrics · doi:10.1067/mpd.2001.111813 · Cited by 84
Self-citationGibson, K. M., Bennett, M. J., Naylor, E., & Morton, D. H. (1998) · The Journal of Pediatrics · doi:10.1016/s0022-3476(98)70032-0 · Cited by 83
Diagnosis of Very Long Chain Acyl-Dehydrogenase Deficiency From an Infant's Newborn Screening Card
Wood, J. C., Magera, M. J., Rinaldo, P., Seashore, M. R., Strauss, A. W., & Friedman, A. (2001) · Pediatrics · doi:10.1542/peds.108.1.e19 · Cited by 62
Reduction of False Negative Results in Screening of Newborns for Homocystinuria
Peterschmitt, M., Simmons, J. R., & Levy, H. L. (1999) · New England Journal of Medicine · doi:10.1056/nejm199911183412103 · Cited by 62
Cited by
Addona, T. A., Abbatiello, S. E., Schilling, B., Skates, S. J., Mani, D. R., Bunk, D. M., Spiegelman, C. H., Zimmerman, L. J., Ham, A.-J. L., Keshishian, H., et al. (2009) · Nature Biotechnology · doi:10.1038/nbt.1546 · Cited by 1,037
Use of Tandem Mass Spectrometry for Multianalyte Screening of Dried Blood Specimens from Newborns
Chace, D. H., Kalas, T. A., & Naylor, E. W. (2003) · Clinical Chemistry · doi:10.1373/clinchem.2003.022178 · Cited by 621
Philip, A. G. S. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000151693.46655.66 · Cited by 592
Metabolic Fingerprinting As A Diagnostic Tool
Ellis, D. I., Dunn, W. B., Griffin, J. L., Allwood, J. W., & Goodacre, R. (2007) · Pharmacogenomics · doi:10.2217/14622416.8.9.1243 · Cited by 396
Acylcarnitines—old actors auditioning for new roles in metabolic physiology
McCoin, C. S., Knotts, T. A., & Adams, S. H. (2015) · Nature Reviews Endocrinology · doi:10.1038/nrendo.2015.129 · Cited by 344
Metadata
- Authors
- Wilcken, B., Wiley, V., Hammond, J., & Carpenter, K.
- Venue
- New England Journal of Medicine
- Publisher
- Massachusetts Medical Society
- 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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