Literature DB >> 27344647

Newborn Screening Programmes in Europe, Arguments and Efforts Regarding Harmonisation: Focus on Organic Acidurias.

Friederike Hörster1, Stefan Kölker2, J Gerard Loeber3, Martina C Cornel4, Georg F Hoffmann2, Peter Burgard2.   

Abstract

BACKGROUND: The state of newborn screening (NBS) programmes for organic acidurias in Europe was assessed by a web-based questionnaire in the EU programme of Community Action in Public Health 2010/2011 among the - at that time - 27 EU member states, candidate countries, potential candidates and three EFTA countries.
RESULTS: Thirty-seven data sets from 39 target countries were analysed. Newborn screening for glutaric aciduria type I (GA-I) was performed in ten, for isovaleric aciduria (IVA) in nine and for methylmalonic aciduria including cblA, cblB, cblC and cblD (MMACBL) as well as for propionic aciduria (PA) in seven countries. Samples were obtained at a median age of 2.5 days and laboratory analysis began at median age of 4.5 days. Positive screening results were mostly confirmed in specialised centres by analysis of organic acids in urine. Confirmation of a positive screening result usually did not start before the second week of life (median ages: 9.5 days [IVA], 9 days [GA-I], 8.5 days [PA, MMACBL]) and was completed early in the third week of life (median ages: 15 days [IVA, PA, MMA], 14.5 days [GA-I]). Treatment was initiated in GA-I and IVA at a median age of 14 days and in MMACBL and PA at a median age of 15 days.
CONCLUSION: NBS for organic acidurias in Europe is variable and less often established than for amino acid disorders. While for GA-I its benefit has already been demonstrated, there is room for debate of NBS for IVA and especially PA and MMACBL.

Entities:  

Keywords:  Europe; Glutaric aciduria type I; Isovaleric aciduria; Methylmalonic acidurias; Newborn screening; Propionic aciduria; cblA, cblB, cblC and cblD

Year:  2016        PMID: 27344647      PMCID: PMC5362556          DOI: 10.1007/8904_2016_537

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  24 in total

1.  Rapid diagnosis of methylmalonic and propionic acidemias: quantitative tandem mass spectrometric analysis of propionylcarnitine in filter-paper blood specimens obtained from newborns.

Authors:  D H Chace; J C DiPerna; T A Kalas; R W Johnson; E W Naylor
Journal:  Clin Chem       Date:  2001-11       Impact factor: 8.327

2.  Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme.

Authors:  Ma Luz Couce; Daisy E Castiñeiras; Ma Dolores Bóveda; Ana Baña; José A Cocho; Agustín J Iglesias; Cristobal Colón; José R Alonso-Fernández; José M Fraga
Journal:  Mol Genet Metab       Date:  2011-09-22       Impact factor: 4.797

3.  Use of guidelines improves the neurological outcome in glutaric aciduria type I.

Authors:  Jana Heringer; S P Nikolas Boy; Regina Ensenauer; Birgit Assmann; Johannes Zschocke; Inga Harting; Thomas Lücke; Esther M Maier; Chris Mühlhausen; Gisela Haege; Georg F Hoffmann; Peter Burgard; Stefan Kölker
Journal:  Ann Neurol       Date:  2010-11       Impact factor: 10.422

4.  Natural history, outcome, and treatment efficacy in children and adults with glutaryl-CoA dehydrogenase deficiency.

Authors:  Stefan Kölker; Sven F Garbade; Cheryl R Greenberg; James V Leonard; Jean-Marie Saudubray; Antonia Ribes; H Serap Kalkanoglu; Allan M Lund; Begoña Merinero; Moacir Wajner; Mónica Troncoso; Monique Williams; John H Walter; Jaume Campistol; Milagros Martí-Herrero; Melissa Caswill; Alberto B Burlina; Florian Lagler; Esther M Maier; Bernd Schwahn; Aysegul Tokatli; Ali Dursun; Turgay Coskun; Ronald A Chalmers; David M Koeller; Johannes Zschocke; Ernst Christensen; Peter Burgard; Georg F Hoffmann
Journal:  Pediatr Res       Date:  2006-04-26       Impact factor: 3.756

Review 5.  Methylmalonic and propionic aciduria.

Authors:  Federica Deodato; Sara Boenzi; Filippo M Santorelli; Carlo Dionisi-Vici
Journal:  Am J Med Genet C Semin Med Genet       Date:  2006-05-15       Impact factor: 3.908

Review 6.  Isovaleric acidemia: new aspects of genetic and phenotypic heterogeneity.

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7.  Newborn screening for isovaleric acidemia using tandem mass spectrometry: data from 1.6 million newborns.

Authors:  Regina Ensenauer; Ralph Fingerhut; Esther M Maier; Roman Polanetz; Bernhard Olgemöller; Wulf Röschinger; Ania C Muntau
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8.  Decline of acute encephalopathic crises in children with glutaryl-CoA dehydrogenase deficiency identified by newborn screening in Germany.

Authors:  Stefan Kölker; Sven F Garbade; Nikolas Boy; Esther M Maier; Thomas Meissner; Chris Mühlhausen; Julia B Hennermann; Thomas Lücke; Johannes Häberle; Jochen Baumkötter; Wolfram Haller; Edith Muller; Johannes Zschocke; Peter Burgard; Georg F Hoffmann
Journal:  Pediatr Res       Date:  2007-09       Impact factor: 3.756

9.  The impact of screening for propionic and methylmalonic acidaemia.

Authors:  James V Leonard; Suresh Vijayaraghavan; John H Walter
Journal:  Eur J Pediatr       Date:  2003-10-30       Impact factor: 3.183

Review 10.  Diagnosis and management of glutaric aciduria type I--revised recommendations.

Authors:  Stefan Kölker; Ernst Christensen; James V Leonard; Cheryl R Greenberg; Avihu Boneh; Alberto B Burlina; Alessandro P Burlina; Marjorie Dixon; Marinus Duran; Angels García Cazorla; Stephen I Goodman; David M Koeller; Mårten Kyllerman; Chris Mühlhausen; Edith Müller; Jürgen G Okun; Bridget Wilcken; Georg F Hoffmann; Peter Burgard
Journal:  J Inherit Metab Dis       Date:  2011-03-23       Impact factor: 4.982

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1.  Is Expanded Newborn Screening Adequate to Detect Indian Biochemical Low Excretor Phenotype Patients of Glutaric Aciduria Type I?

Authors:  Muntaj Shaik; Kruthika-Vinod T P; Mahesh Kamate; Vedamurthy A B
Journal:  Indian J Pediatr       Date:  2019-07-13       Impact factor: 1.967

Review 2.  An Overview of Hypoglycemia in Children Including a Comprehensive Practical Diagnostic Flowchart for Clinical Use.

Authors:  Alberto Casertano; Alessandro Rossi; Simona Fecarotta; Francesco Maria Rosanio; Cristina Moracas; Francesca Di Candia; Giancarlo Parenti; Adriana Franzese; Enza Mozzillo
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Review 3.  Organic acidurias in adults: late complications and management.

Authors:  Ali Tunç Tuncel; Nikolas Boy; Marina A Morath; Friederike Hörster; Ulrike Mütze; Stefan Kölker
Journal:  J Inherit Metab Dis       Date:  2018-01-15       Impact factor: 4.982

4.  Guidelines for the diagnosis and management of methylmalonic acidaemia and propionic acidaemia: First revision.

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5.  Simultaneous determination of 3-hydroxypropionic acid, methylmalonic acid and methylcitric acid in dried blood spots: Second-tier LC-MS/MS assay for newborn screening of propionic acidemia, methylmalonic acidemias and combined remethylation disorders.

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Journal:  PLoS One       Date:  2017-09-15       Impact factor: 3.240

6.  Diagnosis of inborn errors of metabolism within the expanded newborn screening in the Madrid region.

Authors:  Álvaro Martín-Rivada; Laura Palomino Pérez; Pedro Ruiz-Sala; Rosa Navarrete; Ana Cambra Conejero; Pilar Quijada Fraile; Ana Moráis López; Amaya Belanger-Quintana; Elena Martín-Hernández; Marcello Bellusci; Elvira Cañedo Villaroya; Silvia Chumillas Calzada; María Teresa García Silva; Ana Bergua Martínez; Sinziana Stanescu; Mercedes Martínez-Pardo Casanova; Miguel L F Ruano; Magdalena Ugarte; Belén Pérez; Consuelo Pedrón-Giner
Journal:  JIMD Rep       Date:  2022-01-27

7.  Retrospective evaluation of the Dutch pre-newborn screening cohort for propionic acidemia and isolated methylmalonic acidemia: What to aim, expect, and evaluate from newborn screening?

Authors:  Hanneke A Haijes; Femke Molema; Mirjam Langeveld; Mirian C Janssen; Annet M Bosch; Francjan van Spronsen; Margot F Mulder; Nanda M Verhoeven-Duif; Judith J M Jans; Ans T van der Ploeg; Margreet A Wagenmakers; M Estela Rubio-Gozalbo; Martijn C G J Brouwers; Maaike C de Vries; Janneke G Langendonk; Monique Williams; Peter M van Hasselt
Journal:  J Inherit Metab Dis       Date:  2019-12-22       Impact factor: 4.982

  7 in total

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