Literature DB >> 16601872

The tandem mass spectrometry newborn screening experience in North Carolina: 1997-2005.

D M Frazier1, D S Millington, S E McCandless, D D Koeberl, S D Weavil, S H Chaing, J Muenzer.   

Abstract

North Carolina (NC) was the first US state to initiate universal tandem mass spectrometry (MS/MS) newborn screening. This began as a statewide pilot project in 1997 to determine the incidence and feasibility of screening for fatty acid oxidation, organic acid and selected amino acid disorders. The MS/MS analyses were done by a commercial laboratory and all follow-up and confirmatory testing was performed through the NC Newborn Screening (NBS) Program. In April 1999, the NC NBS Laboratory began the MS/MS analyses in-house. Between 28 July 1997 and 28 July 2005, 944,078 infants were screened and 219 diagnoses were confirmed on newborns with elevated screening results, for an overall incidence of 1:4,300. Ninety-nine infants were identified with fatty acid oxidation disorders, 58 with organic acidaemias and 62 with aminoacidopathies. Medium-chain acyl-CoA dehydrogenase deficiency, 3-methylcrotonyl-CoA carboxylase deficiency and disorders of phenylalanine metabolism were the most common disorders detected. Identification of affected infants has allowed retrospective testing of other family members, resulting in an additional 16 diagnoses. Seven neonates died from complications of their metabolic disorders/prematurity despite timely MS/MS screening. In addition, there were six infants who were not identified by elevated NBS results but who presented with symptoms later in infancy. The NC MS/MS NBS Program uses a two-tier system, categorizing results as either 'borderline' or 'diagnostic' elevated, for both the cutoffs and follow-up protocol. Infants with an initial borderline result had only a repeat screen. Infants with a diagnostic or two borderline results were referred for confirmatory testing. The positive predictive value of the NC MS/MS NBS for those infants requiring confirmatory testing was 53% for 2003 and 2004. The success of the NC MS/MS NBS Program in identifying infants with metabolic disorders was dependent on a comprehensive follow-up protocol integrating the public health laboratory and the academic metabolic centres.

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Year:  2006        PMID: 16601872     DOI: 10.1007/s10545-006-0228-9

Source DB:  PubMed          Journal:  J Inherit Metab Dis        ISSN: 0141-8955            Impact factor:   4.982


  13 in total

1.  AN AUTOMATED PROCEDURE FOR BLOOD PHENYLALANINE.

Authors:  J B HILL; G K SUMMER; M W PENDER; N O ROSZEL
Journal:  Clin Chem       Date:  1965-05       Impact factor: 8.327

2.  Tandem mass spectrometry: a new method for acylcarnitine profiling with potential for neonatal screening for inborn errors of metabolism.

Authors:  D S Millington; N Kodo; D L Norwood; C R Roe
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

3.  Tandem mass spectrometric analysis for amino, organic, and fatty acid disorders in newborn dried blood spots: a two-year summary from the New England Newborn Screening Program.

Authors:  T H Zytkovicz; E F Fitzgerald; D Marsden; C A Larson; V E Shih; D M Johnson; A W Strauss; A M Comeau; R B Eaton; G F Grady
Journal:  Clin Chem       Date:  2001-11       Impact factor: 8.327

4.  Glutaric acidemia, type I, missed by newborn screening in an infant with dystonia following promethazine administration.

Authors:  W E Smith; D S Millington; D D Koeberl; P S Lesser
Journal:  Pediatrics       Date:  2001-05       Impact factor: 7.124

5.  Rare disorders of metabolism with elevated butyryl- and isobutyryl-carnitine detected by tandem mass spectrometry newborn screening.

Authors:  Dwight D Koeberl; Sarah P Young; Niels S Gregersen; Jerry Vockley; Wendy E Smith; Daniel Kelly Benjamin; Yan An; Susan D Weavil; Shu H Chaing; Deeksha Bali; Marie T McDonald; Priya S Kishnani; Y-T Chen; David S Millington
Journal:  Pediatr Res       Date:  2003-05-07       Impact factor: 3.756

6.  Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: diagnosis by acylcarnitine analysis in blood.

Authors:  J L Van Hove; W Zhang; S G Kahler; C R Roe; Y T Chen; N Terada; D H Chace; A K Iafolla; J H Ding; D S Millington
Journal:  Am J Hum Genet       Date:  1993-05       Impact factor: 11.025

7.  Expanded newborn screening for inborn errors of metabolism by electrospray ionization-tandem mass spectrometry: results, outcome, and implications.

Authors:  Andreas Schulze; Martin Lindner; Dirk Kohlmüller; Katharina Olgemöller; Ertan Mayatepek; Georg F Hoffmann
Journal:  Pediatrics       Date:  2003-06       Impact factor: 7.124

8.  Screening newborns for inborn errors of metabolism by tandem mass spectrometry.

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Journal:  N Engl J Med       Date:  2003-06-05       Impact factor: 91.245

9.  Evaluation of 3-methylcrotonyl-CoA carboxylase deficiency detected by tandem mass spectrometry newborn screening.

Authors:  D D Koeberl; D S Millington; W E Smith; S D Weavil; J Muenzer; S E McCandless; P S Kishnani; M T McDonald; S Chaing; A Boney; E Moore; D M Frazier
Journal:  J Inherit Metab Dis       Date:  2003       Impact factor: 4.982

10.  Frequencies of inherited organic acidurias and disorders of mitochondrial fatty acid transport and oxidation in Germany.

Authors:  Georg F Hoffmann; Rüdiger von Kries; Daniela Klose; Martin Lindner; Andreas Schulze; Ania C Muntau; Wulf Röschinger; Bernhard Liebl; Ertan Mayatepek; Adelbert A Roscher
Journal:  Eur J Pediatr       Date:  2004-01-09       Impact factor: 3.183

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  50 in total

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Authors:  Yannis L Loukas; Georgios-Stefanos Soumelas; Yannis Dotsikas; Vassiliki Georgiou; Elina Molou; Georgia Thodi; Maria Boutsini; Sofia Biti; Konstantinos Papadopoulos
Journal:  J Inherit Metab Dis       Date:  2010-08-19       Impact factor: 4.982

Review 2.  Potential Uses and Inherent Challenges of Using Genome-Scale Sequencing to Augment Current Newborn Screening.

Authors:  Jonathan S Berg; Cynthia M Powell
Journal:  Cold Spring Harb Perspect Med       Date:  2015-10-05       Impact factor: 6.915

Review 3.  Newborn blood spot screening: new opportunities, old problems.

Authors:  R J Pollitt
Journal:  J Inherit Metab Dis       Date:  2009-05-04       Impact factor: 4.982

4.  Agency discretion and public health service delivery.

Authors:  Pamela J Clouser McCann
Journal:  Health Serv Res       Date:  2009-08-17       Impact factor: 3.402

Review 5.  Genetic screening.

Authors:  Wylie Burke; Beth Tarini; Nancy A Press; James P Evans
Journal:  Epidemiol Rev       Date:  2011-06-27       Impact factor: 6.222

6.  Sequencing from dried blood spots in infants with "false positive" newborn screen for MCAD deficiency.

Authors:  Shawn E McCandless; Ram Chandrasekar; Sharon Linard; Sandra Kikano; Lorrie Rice
Journal:  Mol Genet Metab       Date:  2012-10-24       Impact factor: 4.797

Review 7.  Systematic review and meta-analysis to estimate the birth prevalence of five inherited metabolic diseases.

Authors:  Sowmiya Moorthie; Louise Cameron; Gurdeep S Sagoo; Jim R Bonham; Hilary Burton
Journal:  J Inherit Metab Dis       Date:  2014-07-15       Impact factor: 4.982

8.  Beta-Ketothiolase Deficiency Presenting with Metabolic Stroke After a Normal Newborn Screen in Two Individuals.

Authors:  Monica H Wojcik; Klaas J Wierenga; Lance H Rodan; Inderneel Sahai; Sacha Ferdinandusse; Casie A Genetti; Meghan C Towne; Roy W A Peake; Philip M James; Alan H Beggs; Catherine A Brownstein; Gerard T Berry; Pankaj B Agrawal
Journal:  JIMD Rep       Date:  2017-07-20

9.  Performance of succinylacetone assays and their associated proficiency testing outcomes.

Authors:  B W Adam; E M Hall; N K Meredith; T H Lim; C A Haynes; V R De Jesus; W H Hannon
Journal:  Clin Biochem       Date:  2012-08-11       Impact factor: 3.281

10.  Metabolomics applied to diabetes research: moving from information to knowledge.

Authors:  James R Bain; Robert D Stevens; Brett R Wenner; Olga Ilkayeva; Deborah M Muoio; Christopher B Newgard
Journal:  Diabetes       Date:  2009-11       Impact factor: 9.461

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