Adrenoleukodystrophy Newborn Screening in the Netherlands (SCAN Study): The X-Factor.

X chromosome adrenoleukodystrophy dried bloodspots gender heel prick neonatal newborn screening peroxisomes

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2020
Historique:
received: 08 04 2020
accepted: 25 05 2020
entrez: 7 7 2020
pubmed: 7 7 2020
medline: 7 7 2020
Statut: epublish

Résumé

X-linked adrenoleukodystrophy (ALD) is a devastating metabolic disorder affecting the adrenal glands, brain and spinal cord. Males with ALD are at high risk for developing adrenal insufficiency or progressive cerebral white matter lesions (cerebral ALD) at an early age. If untreated, cerebral ALD is often fatal. Women with ALD are not at risk for adrenal insufficiency or cerebral ALD. Newborn screening for ALD in males enables prospective monitoring and timely therapeutic intervention, thereby preventing irreparable damage and saving lives. The Dutch Ministry of Health adopted the advice of the Dutch Health Council to add a boys-only screen for ALD to the newborn screening panel. The recommendation made by the Dutch Health Council to only screen boys, without gathering any unsolicited findings, posed a challenge. We were invited to set up a prospective pilot study that became known as the SCAN study (SCreening for ALD in the Netherlands). The objectives of the SCAN study are: (1) designing a boys-only screening algorithm that identifies males with ALD and without unsolicited findings; (2) integrating this algorithm into the structure of the Dutch newborn screening program without harming the current newborn screening; (3) assessing the practical and ethical implications of screening only boys for ALD; and (4) setting up a comprehensive follow-up that is both patient- and parent-friendly. We successfully developed and validated a screening algorithm that can be integrated into the Dutch newborn screening program. The core of this algorithm is the "X-counter." The X-counter determines the number of X chromosomes without assessing the presence of a Y chromosome. The X-counter is integrated as second tier in our 4-tier screening algorithm. Furthermore, we ensured that our screening algorithm does not result in unsolicited findings. Finally, we developed a patient- and parent-friendly, multidisciplinary, centralized follow-up protocol. Our boys-only ALD screening algorithm offers a solution for countries that encounter similar ethical considerations, for ALD as well as for other X-linked diseases. For ALD, this alternative boys-only screening algorithm may result in a more rapid inclusion of ALD in newborn screening programs worldwide.

Identifiants

pubmed: 32626714
doi: 10.3389/fcell.2020.00499
pmc: PMC7311642
doi:

Types de publication

Journal Article

Langues

eng

Pagination

499

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2020 Barendsen, Dijkstra, Visser, Alders, Bliek, Boelen, Bouva, van der Crabben, Elsinghorst, van Gorp, Heijboer, Jansen, Jaspers, van Lenthe, Metgod, Mooij, van der Sluijs, van Trotsenburg, Verschoof-Puite, Vaz, Waterham, Wijburg, Engelen, Dekkers and Kemp.

Références

J Inherit Metab Dis. 2017 Nov;40(6):875-881
pubmed: 28677031
Neuropediatrics. 2000 Oct;31(5):227-39
pubmed: 11204280
Mol Genet Metab. 2009 Jul;97(3):212-20
pubmed: 19423374
N Engl J Med. 1990 Jun 28;322(26):1860-6
pubmed: 2348839
Bull World Health Organ. 2008 Apr;86(4):317-9
pubmed: 18438522
Orphanet J Rare Dis. 2014 Jan 13;9:6
pubmed: 24410807
Clin Chim Acta. 1986 Aug 30;159(1):77-82
pubmed: 3757269
Nat Rev Endocrinol. 2016 Oct;12(10):606-15
pubmed: 27312864
Methods Mol Biol. 2017;1595:45-54
pubmed: 28409450
Mol Genet Metab. 2006 Sep-Oct;89(1-2):185-7
pubmed: 16828324
Eur J Pediatr. 2011 Aug;170(8):1049-54
pubmed: 21279382
Brain. 2014 Mar;137(Pt 3):693-706
pubmed: 24480483
Am J Hum Genet. 1995 Aug;57(2):292-301
pubmed: 7668254
Nature. 1993 Feb 25;361(6414):726-30
pubmed: 8441467
Orphanet J Rare Dis. 2012 Aug 13;7:51
pubmed: 22889154
Mol Genet Metab. 1999 Feb;66(2):128-36
pubmed: 10068516
J Pediatr. 2005 Apr;146(4):528-32
pubmed: 15812458
Lab Hematol. 2004;10(1):42-53
pubmed: 15070217
Neurology. 2014 Dec 9;83(24):2227-31
pubmed: 25378668
Pediatr Res. 1984 Mar;18(3):286-90
pubmed: 6728562
Ann Neurol. 2001 Feb;49(2):186-94
pubmed: 11220738
J Pediatr. 2019 Aug;211:211-214
pubmed: 31101408
J Clin Endocrinol Metab. 2018 Nov 1;103(11):4324-4331
pubmed: 30289543
Immunol Allergy Clin North Am. 2019 Nov;39(4):583-591
pubmed: 31563191
Mol Genet Metab. 2017 Dec;122(4):209-215
pubmed: 29089175
Neurology. 1998 Aug;51(2):334 and 9 pages following
pubmed: 9709997
J Inherit Metab Dis. 1996;19(5):667-74
pubmed: 8892025
Mol Genet Metab. 2015 Jan;114(1):46-50
pubmed: 25481105
J Clin Endocrinol Metab. 2019 Jan 1;104(1):118-126
pubmed: 30252065
J Med Genet. 2017 May;54(5):330-337
pubmed: 27799409
Int J Neonatal Screen. 2016 Dec;2(4):
pubmed: 31467997
Orphanet J Rare Dis. 2019 Feb 7;14(1):30
pubmed: 30732635
Mol Genet Metab. 2017 Nov;122(3):134-139
pubmed: 28739201
Nat Clin Pract Neurol. 2007 Mar;3(3):140-51
pubmed: 17342190
Am J Med Genet. 1998 Apr 13;76(5):415-9
pubmed: 9556301
Ann Neurol. 1999 Jan;45(1):100-10
pubmed: 9894883
Biol Blood Marrow Transplant. 2019 Mar;25(3):538-548
pubmed: 30292747
J Sex Res. 2002 Aug;39(3):174-8
pubmed: 12476264
Mol Genet Metab. 2015 Apr;114(4):599-603
pubmed: 25724074
Acta Paediatr Jpn. 1989 Apr;31(2):136-43
pubmed: 2516693

Auteurs

Rinse W Barendsen (RW)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.
Pediatric Metabolic Diseases, Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, Netherlands.

Inge M E Dijkstra (IME)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.

Wouter F Visser (WF)

Centre for Health Protection, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.

Mariëlle Alders (M)

Department of Clinical Genetics, Amsterdam UMC, Amsterdam Reproduction & Development, University of Amsterdam, Amsterdam, Netherlands.

Jet Bliek (J)

Department of Clinical Genetics, Amsterdam UMC, Amsterdam Reproduction & Development, University of Amsterdam, Amsterdam, Netherlands.

Anita Boelen (A)

Department of Clinical Chemistry, Neonatal Screening Laboratory, Endocrine Laboratory, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.

Marelle J Bouva (MJ)

Reference Laboratory for Neonatal Screening, Centre for Health Protection, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.

Saskia N van der Crabben (SN)

Department of Clinical Genetics, Amsterdam UMC, Amsterdam Reproduction & Development, University of Amsterdam, Amsterdam, Netherlands.

Ellen Elsinghorst (E)

Centre for Population Screening, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.

Ankie G M van Gorp (AGM)

Centre for Population Screening, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.

Annemieke C Heijboer (AC)

Department of Clinical Chemistry, Neonatal Screening Laboratory, Endocrine Laboratory, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.
Department of Clinical Chemistry, Endocrine Laboratory, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Mandy Jansen (M)

Department for Vaccine Supply and Prevention Programmes, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.

Yorrick R J Jaspers (YRJ)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.

Henk van Lenthe (H)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.

Ingrid Metgod (I)

Department of Clinical Chemistry, Neonatal Screening Laboratory, Endocrine Laboratory, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.
Department of Clinical Chemistry, Endocrine Laboratory, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, Vrije Universiteit Amsterdam, Amsterdam, Netherlands.

Christiaan F Mooij (CF)

Department of Pediatric Endocrinology, Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, Netherlands.

Elise H C van der Sluijs (EHC)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.

A S Paul van Trotsenburg (ASP)

Department of Pediatric Endocrinology, Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, Netherlands.

Rendelien K Verschoof-Puite (RK)

Department for Vaccine Supply and Prevention Programmes, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.

Frédéric M Vaz (FM)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.

Hans R Waterham (HR)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.

Frits A Wijburg (FA)

Pediatric Metabolic Diseases, Amsterdam UMC, Emma Children's Hospital, University of Amsterdam, Amsterdam, Netherlands.

Marc Engelen (M)

Department of Pediatric Neurology, Amsterdam UMC, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam Neuroscience, University of Amsterdam, Amsterdam, Netherlands.

Eugènie Dekkers (E)

Centre for Population Screening, National Institute for Public Health and the Environment (RIVM), Bilthoven, Netherlands.

Stephan Kemp (S)

Department of Clinical Chemistry, Laboratory Genetic Metabolic Diseases, Amsterdam UMC, Amsterdam Gastroenterology and Metabolism, University of Amsterdam, Amsterdam, Netherlands.
Department of Pediatric Neurology, Amsterdam UMC, Amsterdam Leukodystrophy Center, Emma Children's Hospital, Amsterdam Neuroscience, University of Amsterdam, Amsterdam, Netherlands.

Classifications MeSH