Literature DB >> 28733853

Cerebral magnetic resonance findings during enzyme replacement therapy in mucopolysaccharidosis.

Yoshiko Matsubara1,2, Osamu Miyazaki3, Motomichi Kosuga4, Torayuki Okuyama5, Shunsuke Nosaka3.   

Abstract

BACKGROUND: Although enzyme replacement therapy (ERT) is an effective treatment for mucopolysaccharidosis (MPS) types I, II, IVA and VI, its effectiveness in children with central nervous system (CNS) disorders is said to be poor because the blood-brain barrier cannot be penetrated by ERT drugs.
OBJECTIVE: To assess CNS involvement in mucopolysaccharidosis at the start of enzyme replacement therapy and to investigate the time course of ERT in the central nervous system.
MATERIALS AND METHODS: We performed brain MRI in 17 children and young adults who underwent ERT. The clinical severity was classified as attenuated or severe by a specialist pediatrician, based on the clinical symptoms and genotypes. At the start of ERT, we scored nine parameters using two- or three-point scales based on the severity of the disease revealed on MRI scans. After the start of ERT, we compared the initial and follow-up MRI scans, and classified the findings as no change, improved or worse. We then compared the results with the changes in clinical findings.
RESULTS: At the start of ERT, comparison of the clinical symptoms and image scores revealed differences between severe and attenuated mucopolysaccharidosis. The scores in patients with severe MPS ranged from 9 to 16 (mean 12.2); for patients with attenuated MPS, they ranged from 2 to 11 (mean 6.4). Images of the four patients with severe MPS showed ventricular dilation and brain atrophy. Such findings were made in only 2 of 13 patients with attenuated MPS. The results after the start of ERT showed that 11/17 (65%) patients manifested improvement or no change. All five patients with MPS I experienced improvement in some regions. There were no new lesions. One patient with MPS II experienced worsening of his CNS symptoms, and his MRI findings revealed more severe ventricular dilation, brain atrophy and white matter lesions.
CONCLUSION: Ventricular dilation and brain atrophy on imaging studies might represent useful markers in predicting the severity of mucopolysaccharidosis and worsening of CNS symptoms. Enzyme replacement therapy improves CNS images in MPS I and has an inhibitory effect on the occurrence of new lesions in MPS II.

Entities:  

Keywords:  Brain; Children; Enzyme replacement therapy; Magnetic resonance imaging; Mucopolysaccharidosis; Phenotype; Young adults

Mesh:

Year:  2017        PMID: 28733853     DOI: 10.1007/s00247-017-3935-5

Source DB:  PubMed          Journal:  Pediatr Radiol        ISSN: 0301-0449


  16 in total

1.  Brain MRI findings in patients with mucopolysaccharidosis types I and II and mild clinical presentation.

Authors:  M Gisele Matheus; Mauricio Castillo; J Keith Smith; Diane Armao; Diane Towle; Joseph Muenzer
Journal:  Neuroradiology       Date:  2004-06-17       Impact factor: 2.804

Review 2.  Brain and spinal MR imaging findings in mucopolysaccharidoses: a review.

Authors:  D I Zafeiriou; S P Batzios
Journal:  AJNR Am J Neuroradiol       Date:  2012-07-12       Impact factor: 3.825

3.  Brain and spine MRI features of Hunter disease: frequency, natural evolution and response to therapy.

Authors:  Renzo Manara; Elena Priante; Marco Grimaldi; Lucia Santoro; Luca Astarita; Rita Barone; Daniela Concolino; Maja Di Rocco; Maria Alice Donati; Simona Fecarotta; Anna Ficcadenti; Agata Fiumara; Francesca Furlan; Irene Giovannini; Franco Lilliu; Rodica Mardari; Gabriele Polonara; Elena Procopio; Angelica Rampazzo; Andrea Rossi; Graziolina Sanna; Rossella Parini; Maurizio Scarpa
Journal:  J Inherit Metab Dis       Date:  2011-04-05       Impact factor: 4.982

Review 4.  Enzyme replacement therapy in mucopolysaccharidosis type I.

Authors:  E Miebach
Journal:  Acta Paediatr Suppl       Date:  2005-03

5.  Mucopolysaccharidosis: thickening of dura mater at the craniocervical junction and other CT/MRI findings.

Authors:  A Taccone; P Tortori Donati; A Marzoli; A Dell'Acqua; R Gatti; D Leone
Journal:  Pediatr Radiol       Date:  1993

6.  Regression of ventriculomegaly following medical management of a patient with Hurler syndrome.

Authors:  Jennifer Liang; Ash Singhal
Journal:  J Neurosurg Pediatr       Date:  2016-01-08       Impact factor: 2.375

7.  Dilated perivascular spaces: an informative radiologic finding in Sanfilippo syndrome type A.

Authors:  Simay Kara; Elliott H Sherr; A James Barkovich
Journal:  Pediatr Neurol       Date:  2008-05       Impact factor: 3.372

8.  Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II.

Authors:  Raymond Y Wang; Elizabeth Jane Cambray-Forker; Kirk Ohanian; David S Karlin; Kelly K Covault; Philip H Schwartz; Jose E Abdenur
Journal:  Mol Genet Metab       Date:  2009-08-05       Impact factor: 4.797

Review 9.  Recognition and diagnosis of mucopolysaccharidosis II (Hunter syndrome).

Authors:  Rick Martin; Michael Beck; Christine Eng; Roberto Giugliani; Paul Harmatz; Verónica Muñoz; Joseph Muenzer
Journal:  Pediatrics       Date:  2008-02       Impact factor: 7.124

10.  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

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  1 in total

1.  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

  1 in total

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