Literature DB >> 14714182

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

Georg F Hoffmann1, Rüdiger von Kries, Daniela Klose, Martin Lindner, Andreas Schulze, Ania C Muntau, Wulf Röschinger, Bernhard Liebl, Ertan Mayatepek, Adelbert A Roscher.   

Abstract

UNLABELLED: The lack of epidemiological data on the frequency and/or burden of organic acidurias (OA) and mitochondrial fatty acid transport and oxidation disorders (mtFATOD) is one reason for hesitation to expand newborn screening (NBS) by tandem mass spectrometry (MS-MS). From 1999 to 2000, the frequency of ten potentially treatable OA and mtFATOD was assessed by active nation-wide surveillance on cases presenting with clinical symptoms using the German Paediatric Surveillance Unit (ESPED) system. Case ascertainment was complemented by a second independent source: 3-monthly inquiries in the metabolic laboratories performing secondary selected screening for OA and mtFATOD. Frequency estimates for clinically symptomatic cases older than 7 days in a birth cohort of 844,575 conventionally screened children was compared to the frequency found in a cohort of 382,247 screened by MS-MS in Bavaria and Baden-Württemberg. The overall frequency of the ten conditions considered was 1:8,000 (95% CI 1:11,000-1:6,000) by MS-MS as compared to 1:23,000 (95% CI 1:36,000-1:17,000) in symptomatic cases presenting mainly with metabolic crisis. The contributions of medium-chain acyl-CoA dehydrogenase deficiency (MCADD), other mtFATOD and OA were 29, 4 and 13 among the 46 cases identified by MS-MS, and 19, 1 and 13 among the 33 clinically symptomatic cases, respectively. Acute metabolic crisis, with a lethal outcome in four patients, was reported for 22/33 clinically symptomatic cases. No clinically symptomatic cases were reported from cohorts with screened by MS-MS.
CONCLUSION: ten potentially treatable organic acidurias and mitochondrial fatty acid transport and oxidations disorders were more common than phenylketonuria with organic acidurias accounting for 28% of the cases detected by newborn screening and 39% of the cases identified on high risk screening. These conditions were related to considerable morbidity and mortality. Considerations for their inclusion in expanded newborn screening programmes might be warranted.

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Year:  2004        PMID: 14714182     DOI: 10.1007/s00431-003-1246-3

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  10 in total

1.  Screening for inherited metabolic disease in newborn infants using tandem mass spectrometry.

Authors:  James V Leonard; Carol Dezateux
Journal:  BMJ       Date:  2002-01-05

2.  Newborn screening by tandem mass spectrometry: a new era.

Authors:  H L Levy
Journal:  Clin Chem       Date:  1998-12       Impact factor: 8.327

Review 3.  Newborn screening for inborn errors of metabolism: a systematic review.

Authors:  C A Seymour; M J Thomason; R A Chalmers; G M Addison; M D Bain; F Cockburn; P Littlejohns; J Lord; A H Wilcox
Journal:  Health Technol Assess       Date:  1997       Impact factor: 4.014

4.  Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosis.

Authors:  C J Wilson; M P Champion; J E Collins; P T Clayton; J V Leonard
Journal:  Arch Dis Child       Date:  1999-05       Impact factor: 3.791

5.  Ascertainment corrected rates: applications of capture-recapture methods.

Authors:  D J McCarty; E S Tull; C S Moy; C K Kwoh; R E LaPorte
Journal:  Int J Epidemiol       Date:  1993-06       Impact factor: 7.196

Review 6.  Evaluating newborn screening programmes based on dried blood spots: future challenges.

Authors:  C Dezateux
Journal:  Br Med Bull       Date:  1998       Impact factor: 4.291

7.  Neonatal screening for medium-chain acyl-CoA dehydrogenase deficiency.

Authors:  M Pourfarzam; A Morris; M Appleton; A Craft; K Bartlett
Journal:  Lancet       Date:  2001-09-29       Impact factor: 79.321

8.  Prospective surveillance study of medium chain acyl-CoA dehydrogenase deficiency in the UK.

Authors:  R J Pollitt; J V Leonard
Journal:  Arch Dis Child       Date:  1998-08       Impact factor: 3.791

9.  Intellectual performance of children with maple syrup urine disease.

Authors:  C Hilliges; D Awiszus; U Wendel
Journal:  Eur J Pediatr       Date:  1993-02       Impact factor: 3.183

Review 10.  Selective screening for inborn errors of metabolism--past, present and future.

Authors:  G F Hoffmann
Journal:  Eur J Pediatr       Date:  1994       Impact factor: 3.183

  10 in total
  21 in total

Review 1.  The clinical manifestation of MCAD deficiency: challenges towards adulthood in the screened population.

Authors:  Ulrich A Schatz; Regina Ensenauer
Journal:  J Inherit Metab Dis       Date:  2010-06-08       Impact factor: 4.982

2.  Impact of inborn errors of metabolism on admission and mortality in a pediatric intensive care unit.

Authors:  Philippe Jouvet; Guy Touati; Fabrice Lesage; Laurent Dupic; Marisa Tucci; Jean Marie Saudubray; Philippe Hubert
Journal:  Eur J Pediatr       Date:  2006-08-29       Impact factor: 3.183

3.  Acceptance of extended newborn screening: the problem of parental non-compliance.

Authors:  Adrian C Sewell; Boris Gebhardt; Jürgen Herwig; Ernst W Rauterberg
Journal:  Eur J Pediatr       Date:  2004-12       Impact factor: 3.183

4.  Beyond counting cases: public health impacts of national Paediatric Surveillance Units.

Authors:  D Grenier; E J Elliott; Y Zurynski; R Rodrigues Pereira; M Preece; R Lynn; R von Kries; H Zimmermann; N P Dickson; D Virella
Journal:  Arch Dis Child       Date:  2006-12-11       Impact factor: 3.791

5.  Expanded newborn screening in Europe 2007.

Authors:  O A Bodamer; G F Hoffmann; M Lindner
Journal:  J Inherit Metab Dis       Date:  2007-07-23       Impact factor: 4.982

Review 6.  Fetal fatty acid oxidation disorders, their effect on maternal health and neonatal outcome: impact of expanded newborn screening on their diagnosis and management.

Authors:  Prem S Shekhawat; Dietrich Matern; Arnold W Strauss
Journal:  Pediatr Res       Date:  2005-04-06       Impact factor: 3.756

7.  Incidence of medium-chain acyl-CoA dehydrogenase deficiency in Canada using the Canadian Paediatric Surveillance Program: Role of newborn screening.

Authors:  Chitra Prasad; Kathy N Speechley; Sarah Dyack; Charles A Rupar; Pranesh Chakraborty; Jonathan B Kronick
Journal:  Paediatr Child Health       Date:  2012-04       Impact factor: 2.253

Review 8.  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

9.  Clinical and biological features at diagnosis in mitochondrial fatty acid beta-oxidation defects: a French pediatric study of 187 patients.

Authors:  Julien Baruteau; Philippe Sachs; Pierre Broué; Michèle Brivet; Hendy Abdoul; Christine Vianey-Saban; Hélène Ogier de Baulny
Journal:  J Inherit Metab Dis       Date:  2012-10-03       Impact factor: 4.982

10.  Cognitive functioning and psychiatric disorders in children with a metabolic disease.

Authors:  Annik Simons; François Eyskens; Ann De Groof; Ellen Van Diest; Dirk Deboutte; Robert Vermeiren
Journal:  Eur Child Adolesc Psychiatry       Date:  2006-03-10       Impact factor: 4.785

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