Literature DB >> 28125077

Cognitive outcomes and age of detection of severe mucopolysaccharidosis type 1.

Scott D Grosse1, Wendy K K Lam2, Lisa D Wiggins1, Alex R Kemper2.   

Abstract

The US Secretary of Health and Human Services recommended in February 2016 that mucopolysaccharidosis type 1 (MPS I) be added to the recommended uniform screening panel for state newborn screening programs. One of the key factors in this decision was the evidence suggesting that earlier treatment with hematopoietic cell transplantation (HCT) for the most severe form, Hurler syndrome (MPS IH), would lead to improved cognitive outcomes. Consistent evidence from peer-reviewed studies suggests that transplantation in the first year of life is associated with improved developmental quotient or intelligence quotient and continued cognitive growth, with earlier age of treatment associated with improved outcomes. However, available evidence suggests that cognitive functioning and attention can still lag behind unaffected age-matched children, leading to the need for special education services. Verbal and nonverbal cognitive abilities outcomes may be affected differently by HCT. With the recent addition of MPS I to the recommended uniform screening panel, future work is needed to evaluate the impact of earlier, presymptomatic detection and treatment initiation and other supportive therapies on cognitive outcomes.Genet Med advance online publication 26 January 2017.

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Mesh:

Year:  2017        PMID: 28125077      PMCID: PMC5763496          DOI: 10.1038/gim.2016.223

Source DB:  PubMed          Journal:  Genet Med        ISSN: 1098-3600            Impact factor:   8.822


  26 in total

Review 1.  The clinical outcome of Hurler syndrome after stem cell transplantation.

Authors:  Mieke Aldenhoven; Jaap Jan Boelens; Tom J de Koning
Journal:  Biol Blood Marrow Transplant       Date:  2008-05       Impact factor: 5.742

2.  Long-term outcome of Hurler syndrome patients after hematopoietic cell transplantation: an international multicenter study.

Authors:  Mieke Aldenhoven; Robert F Wynn; Paul J Orchard; Anne O'Meara; Paul Veys; Alain Fischer; Vassili Valayannopoulos; Benedicte Neven; Attilio Rovelli; Vinod K Prasad; Jakub Tolar; Heather Allewelt; Simon A Jones; Rossella Parini; Marleen Renard; Victoria Bordon; Nico M Wulffraat; Tom J de Koning; Elsa G Shapiro; Joanne Kurtzberg; Jaap Jan Boelens
Journal:  Blood       Date:  2015-01-26       Impact factor: 22.113

Review 3.  Early initiation of enzyme replacement therapy for the mucopolysaccharidoses.

Authors:  Joseph Muenzer
Journal:  Mol Genet Metab       Date:  2013-12-11       Impact factor: 4.797

4.  Enzyme replacement is associated with better cognitive outcomes after transplant in Hurler syndrome.

Authors:  Julie B Eisengart; Kyle D Rudser; Jakub Tolar; Paul J Orchard; Teresa Kivisto; Richard S Ziegler; Chester B Whitley; Elsa G Shapiro
Journal:  J Pediatr       Date:  2012-09-10       Impact factor: 4.406

5.  Neurocognition across the spectrum of mucopolysaccharidosis type I: Age, severity, and treatment.

Authors:  Elsa G Shapiro; Igor Nestrasil; Kyle Rudser; Kathleen Delaney; Victor Kovac; Alia Ahmed; Brianna Yund; Paul J Orchard; Julie Eisengart; Gregory R Niklason; Julian Raiman; Eva Mamak; Morton J Cowan; Mara Bailey-Olson; Paul Harmatz; Suma P Shankar; Stephanie Cagle; Nadia Ali; Robert D Steiner; Jeffrey Wozniak; Kelvin O Lim; Chester B Whitley
Journal:  Mol Genet Metab       Date:  2015-06-17       Impact factor: 4.797

Review 6.  Laronidase (Aldurazyme): enzyme replacement therapy for mucopolysaccharidosis type I.

Authors:  Gregory M Pastores
Journal:  Expert Opin Biol Ther       Date:  2008-07       Impact factor: 4.388

7.  Outcome of 27 patients with Hurler's syndrome transplanted from either related or unrelated haematopoietic stem cell sources.

Authors:  G Souillet; N Guffon; I Maire; M Pujol; P Taylor; F Sevin; N Bleyzac; C Mulier; A Durin; K Kebaili; C Galambrun; Y Bertrand; R Froissart; C Dorche; L Gebuhrer; C Garin; J Berard; P Guibaud
Journal:  Bone Marrow Transplant       Date:  2003-06       Impact factor: 5.483

8.  Transplantation in inborn errors of metabolism: current considerations and future perspectives.

Authors:  Jaap Jan Boelens; Paul J Orchard; Robert F Wynn
Journal:  Br J Haematol       Date:  2014-07-30       Impact factor: 6.998

9.  Cognitive and neuroradiological improvement in three patients with attenuated MPS I treated by laronidase.

Authors:  V Valayannopoulos; N Boddaert; V Barbier; M Le Merrer; C Caillaud; P de Lonlay
Journal:  Mol Genet Metab       Date:  2010-01-04       Impact factor: 4.797

10.  Early treatment with laronidase improves clinical outcomes in patients with attenuated MPS I: a retrospective case series analysis of nine sibships.

Authors:  Nouriya A Al-Sannaa; Luisa Bay; Deborah S Barbouth; Youssef Benhayoun; Cyril Goizet; Norberto Guelbert; Simon A Jones; Sandra Obikawa Kyosen; Ana Maria Martins; Chanika Phornphutkul; Celia Reig; Rebecca Pleat; Shari Fallet; Iva Ivanovska Holder
Journal:  Orphanet J Rare Dis       Date:  2015-10-07       Impact factor: 4.123

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  13 in total

1.  Quantifying medical manifestations in Hurler syndrome with the infant physical symptom score: associations with long-term physical and adaptive outcomes.

Authors:  Alia Ahmed; Kyle Rudser; Kelly E King; Julie B Eisengart; Paul J Orchard; Elsa Shapiro; Chester B Whitley
Journal:  Mol Genet Metab       Date:  2022-03-10       Impact factor: 4.204

2.  Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood-onset beta-mannosidosis.

Authors:  Troy C Lund; Weston P Miller; Julie B Eisengart; Katrina Simmons; Laura Pollard; Deborah L Renaud; David A Wenger; Marc C Patterson; Paul J Orchard
Journal:  Mol Genet Genomic Med       Date:  2019-05-21       Impact factor: 2.183

3.  Long term disease burden post-transplantation: three decades of observations in 25 Hurler patients successfully treated with hematopoietic stem cell transplantation (HSCT).

Authors:  N Guffon; M Pettazzoni; N Pangaud; C Garin; G Lina-Granade; C Plault; C Mottolese; R Froissart; A Fouilhoux
Journal:  Orphanet J Rare Dis       Date:  2021-01-31       Impact factor: 4.123

4.  Is hematopoietic stem cell transplantation a therapeutic option for mucolipidosis type II?

Authors:  Luise Sophie Ammer; Sandra Pohl; Sandra Rafaela Breyer; Charlotte Aries; Jonas Denecke; Anna Perez; Martin Petzoldt; Johanna Schrum; Ingo Müller; Nicole Maria Muschol
Journal:  Mol Genet Metab Rep       Date:  2021-01-14

5.  Beneath the floor: re-analysis of neurodevelopmental outcomes in untreated Hurler syndrome.

Authors:  Elsa G Shapiro; Chester B Whitley; Julie B Eisengart
Journal:  Orphanet J Rare Dis       Date:  2018-05-11       Impact factor: 4.123

6.  Long-term cognitive and somatic outcomes of enzyme replacement therapy in untransplanted Hurler syndrome.

Authors:  Julie B Eisengart; Jeanine Jarnes; Alia Ahmed; Igor Nestrasil; Richard Ziegler; Kathleen Delaney; Elsa Shapiro; Chester Whitley
Journal:  Mol Genet Metab Rep       Date:  2017-09-27

Review 7.  Neurobehavioral phenotypes of neuronopathic mucopolysaccharidoses.

Authors:  Rita Barone; Alessandra Pellico; Annarita Pittalà; Serena Gasperini
Journal:  Ital J Pediatr       Date:  2018-11-16       Impact factor: 2.638

8.  Long-term outcomes of systemic therapies for Hurler syndrome: an international multicenter comparison.

Authors:  Julie B Eisengart; Kyle D Rudser; Yong Xue; Paul Orchard; Weston Miller; Troy Lund; Ans Van der Ploeg; Jean Mercer; Simon Jones; Karl Eugen Mengel; Seyfullah Gökce; Nathalie Guffon; Roberto Giugliani; Carolina F M de Souza; Elsa G Shapiro; Chester B Whitley
Journal:  Genet Med       Date:  2018-03-08       Impact factor: 8.822

9.  The Value of Case Reports in Systematic Reviews from Rare Diseases. The Example of Enzyme Replacement Therapy (ERT) in Patients with Mucopolysaccharidosis Type II (MPS-II).

Authors:  Miguel Sampayo-Cordero; Bernat Miguel-Huguet; Andrea Malfettone; José Manuel Pérez-García; Antonio Llombart-Cussac; Javier Cortés; Almudena Pardo; Jordi Pérez-López
Journal:  Int J Environ Res Public Health       Date:  2020-09-10       Impact factor: 3.390

10.  Case Report: Cerebral Revascularization in a Child With Mucopolysaccharidosis Type I.

Authors:  Nathan Grant; J Michael Taylor; Zach Plummer; Kasiani Myers; Thomas Burrow; Lori Luchtman-Jones; Anna Byars; Adrienne Hammill; Katie Wusick; Edward Smith; James Leach; Sudhakar Vadivelu
Journal:  Front Pediatr       Date:  2021-06-10       Impact factor: 3.418

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