Literature DB >> 20373143

Newborn screening for disorders of fatty-acid oxidation: experience and recommendations from an expert meeting.

Martin Lindner1, Georg F Hoffmann, Dietrich Matern.   

Abstract

Experience with new-born screening (NBS) for disorders of fatty-acid oxidation (FAOD) is now becoming available from an increasing number of programs worldwide. The spectrum of FAOD differs widely between ethnic groups. Incidence calculations from reports from Australia, Germany, and the USA of a total of 5,256,999 newborns give a combined incidence of all FAOD of approximately 1:9,300. However, it appears to be much lower in Asians. Consequently, a significant prevalence and evidence for a clear benefit of NBS is proven for medium-chain acyl-CoA dehydrogenase deficiency (MCAD) only in countries with a high percentage of Caucasians, with very-long-chain acyl-CoA dehydrogenase deficiency (VLCAD) and long-chain 3-hydroxy acyl-CoA dehydrogenase deficiency (LCHAD) being additional candidates. The long-term benefit for many disorders has still to be evaluated and will require international collaboration, especially for the rarest disorders. Short-chain acyl-CoA dehydrogenase deficiency (SCAD) [as well as Systemic carnitine transporter deficiency (CTD) and dienoyl-CoA reductase deficiency (DE-RED)] are conditions of uncertain clinical significance, but most FAOD have a spectrum of clinical presentations (healthy-death). Confirmatory diagnostic procedures should be agreed upon to ensure international comparability of results and evidence-based modifications. The case of short-chain acyl-CoA dehydrogenase deficiency (SCAD) deficiency shows that even inclusion of conditions without a clearly known natural course may prove useful with respect to gain of knowledge and consecutive exclusion of a biochemical abnormality without clinical significance, although this line of argument implies the existence of structured follow-up programs and bears ethical controversies. As a final conclusion, the accumulated evidence suggests all FAOD should to be included into tandem mass spectrometry (MS/MS)-based NBS programs provided sufficient laboratory performance is guaranteed.

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Year:  2010        PMID: 20373143     DOI: 10.1007/s10545-010-9076-8

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


  13 in total

1.  Making the case for objective performance metrics in newborn screening by tandem mass spectrometry.

Authors:  Piero Rinaldo; Saba Zafari; Silvia Tortorelli; Dietrich Matern
Journal:  Ment Retard Dev Disabil Res Rev       Date:  2006

2.  Clinical, biochemical, and genetic heterogeneity in short-chain acyl-coenzyme A dehydrogenase deficiency.

Authors:  Bianca T van Maldegem; Marinus Duran; Ronald J A Wanders; Klary E Niezen-Koning; Marije Hogeveen; Lodewijk Ijlst; Hans R Waterham; Frits A Wijburg
Journal:  JAMA       Date:  2006-08-23       Impact factor: 56.272

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

Review 4.  Neonatal screening for congenital adrenal hyperplasia.

Authors:  Hetty J van der Kamp; Jan M Wit
Journal:  Eur J Endocrinol       Date:  2004-11       Impact factor: 6.664

5.  Short-chain acyl-CoA dehydrogenase (SCAD) deficiency: an examination of the medical and neurodevelopmental characteristics of 14 cases identified through newborn screening or clinical symptoms.

Authors:  S E Waisbren; H L Levy; M Noble; D Matern; N Gregersen; K Pasley; D Marsden
Journal:  Mol Genet Metab       Date:  2008-08-03       Impact factor: 4.797

6.  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

7.  Dissection of biochemical borderline phenotypes in carriers and genetic variants of medium-chain acyl-CoA dehyrogenase deficiency: implications for newborn screening [corrected].

Authors:  E M Maier; J Pongratz; A C Muntau; B Liebl; U Nennstiel-Ratzel; U Busch; R Fingerhut; B Olgemöller; A A Roscher; W Röschinger
Journal:  Clin Genet       Date:  2009-08       Impact factor: 4.438

8.  VLCAD deficiency: pitfalls in newborn screening and confirmation of diagnosis by mutation analysis.

Authors:  A Boneh; B S Andresen; N Gregersen; M Ibrahim; N Tzanakos; H Peters; J Yaplito-Lee; J J Pitt
Journal:  Mol Genet Metab       Date:  2006-02-20       Impact factor: 4.797

9.  Cost-effectiveness of neonatal screening for medium chain acyl-CoA dehydrogenase deficiency: the homogeneous population of The Netherlands.

Authors:  Christian S van der Hilst; Terry G J Derks; Dirk-Jan Reijngoud; G Peter A Smit; Elisabeth M TenVergert
Journal:  J Pediatr       Date:  2007-08       Impact factor: 4.406

10.  Novel mutations causing medium chain acyl-CoA dehydrogenase deficiency: under-representation of the common c.985 A > G mutation in the New York state population.

Authors:  Matthew J Nichols; Carlos A Saavedra-Matiz; Kenneth A Pass; Michele Caggana
Journal:  Am J Med Genet A       Date:  2008-03-01       Impact factor: 2.802

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  60 in total

1.  VLCAD enzyme activity determinations in newborns identified by screening: a valuable tool for risk assessment.

Authors:  Lars Hoffmann; Ulrike Haussmann; Martina Mueller; Ute Spiekerkoetter
Journal:  J Inherit Metab Dis       Date:  2011-09-20       Impact factor: 4.982

Review 2.  Cell and gene therapy for genetic diseases: inherited disorders affecting the lung and those mimicking sudden infant death syndrome.

Authors:  Allison M Keeler; Terence R Flotte
Journal:  Hum Gene Ther       Date:  2012-06       Impact factor: 5.695

3.  Recurrent ACADVL molecular findings in individuals with a positive newborn screen for very long chain acyl-coA dehydrogenase (VLCAD) deficiency in the United States.

Authors:  Marcus J Miller; Lindsay C Burrage; James B Gibson; Meghan E Strenk; Edward J Lose; David P Bick; Sarah H Elsea; V Reid Sutton; Qin Sun; Brett H Graham; William J Craigen; Victor Wei Zhang; Lee-Jun C Wong
Journal:  Mol Genet Metab       Date:  2015-09-02       Impact factor: 4.797

4.  Toxicity of octanoate and decanoate in rat peripheral tissues: evidence of bioenergetic dysfunction and oxidative damage induction in liver and skeletal muscle.

Authors:  Giselli Scaini; Kellen R Simon; Anelise M Tonin; Estela N B Busanello; Alana P Moura; Gustavo C Ferreira; Moacir Wajner; Emilio L Streck; Patrícia F Schuck
Journal:  Mol Cell Biochem       Date:  2011-10-21       Impact factor: 3.396

5.  Normal Levels of Plasma Free Carnitine and Acylcarnitines in Follow-Up Samples from a Presymptomatic Case of Carnitine Palmitoyl Transferase 1 (CPT1) Deficiency Detected Through Newborn Screening in Denmark.

Authors:  Luise Borch; Allan Meldgaard Lund; Flemming Wibrand; Ernst Christensen; Charlotte Søndergaard; Birthe Gahrn; David Michael Hougaard; Brage Storstein Andresen; Niels Gregersen; Rikke Katrine Jentoft Olsen
Journal:  JIMD Rep       Date:  2011-09-22

6.  Prevalence of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency in Estonia.

Authors:  K Joost; K Ounap; R Zordania; M-L Uudelepp; R K Olsen; K Kall; K Kilk; U Soomets; T Kahre
Journal:  JIMD Rep       Date:  2011-09-06

Review 7.  Short-chain acyl-CoA dehydrogenase deficiency: from gene to cell pathology and possible disease mechanisms.

Authors:  Zahra Nochi; Rikke Katrine Jentoft Olsen; Niels Gregersen
Journal:  J Inherit Metab Dis       Date:  2017-05-17       Impact factor: 4.982

8.  Clinical features and mutations in seven Chinese patients with very long chain acyl-CoA dehydrogenase deficiency.

Authors:  Rui-Nan Zhang; Yi-Fan Li; Wen-Juan Qiu; Jun Ye; Lian-Shu Han; Hui-Wen Zhang; Na Lin; Xue-Fan Gu
Journal:  World J Pediatr       Date:  2014-05-07       Impact factor: 2.764

9.  Molecular and cellular pathology of very-long-chain acyl-CoA dehydrogenase deficiency.

Authors:  Manuel Schiff; Al-Walid Mohsen; Anuradha Karunanidhi; Elizabeth McCracken; Renita Yeasted; Jerry Vockley
Journal:  Mol Genet Metab       Date:  2013-02-13       Impact factor: 4.797

10.  Sports in LCHAD Deficiency: Maximal Incremental and Endurance Exercise Tests in a 13-Year-Old Patient with Long-Chain 3-Hydroxy Acyl-CoA Dehydrogenase Deficiency (LCHADD) and Heptanoate Treatment.

Authors:  D Karall; G Mair; U Albrecht; K Niedermayr; T Karall; W Schobersberger; S Scholl-Bürgi
Journal:  JIMD Rep       Date:  2014-07-06
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