Intrathecal enzyme replacement therapy reverses cognitive decline in mucopolysaccharidosis type I. Issue 3 (17th February 2017)
- Record Type:
- Journal Article
- Title:
- Intrathecal enzyme replacement therapy reverses cognitive decline in mucopolysaccharidosis type I. Issue 3 (17th February 2017)
- Main Title:
- Intrathecal enzyme replacement therapy reverses cognitive decline in mucopolysaccharidosis type I
- Authors:
- Nestrasil, Igor
Shapiro, Elsa
Svatkova, Alena
Dickson, Patricia
Chen, Agnes
Wakumoto, Amy
Ahmed, Alia
Stehel, Edward
McNeil, Sarah
Gravance, Curtis
Maher, Elizabeth - Abstract:
- Abstract : Mucopolysaccharidosis type I (MPS I) is an inherited lysosomal storage disease that seriously affects the brain. Severity of neurocognitive symptoms in attenuated MPS subtype (MPS IA) broadly varies partially, due to restricted permeability of blood‐brain barrier (BBB) which limits treatment effects of intravenously applied α‐L‐iduronidase (rhIDU) enzyme. Intrathecal (IT) rhIDU application as a possible solution to circumvent BBB improved brain outcomes in canine models; therefore, our study quantifies effects of IT rhIDU on brain structure and function in an MPS IA patient with previous progressive cognitive decline. Neuropsychological testing and MRIs were performed twice prior (baseline, at 1 year) and twice after initiating IT rhIDU (at 2nd and 3rd years). The difference between pre‐ and post‐treatment means was evaluated as a percentage of the change. Neurocognitive performance improved particularly in memory tests and resulted in improved school performance after IT rhIDU treatment. White matter (WM) integrity improved together with an increase of WM and corpus callosum volumes. Hippocampal and gray matter volume decreased which may either parallel reduction of glycosaminoglycan storage or reflect typical longitudinal brain changes in early adulthood. In conclusion, our outcomes suggest neurological benefits of IT rhIDU compared to the intravenous administration on brain structure and function in a single MPS IA patient. © 2017 The Authors. American JournalAbstract : Mucopolysaccharidosis type I (MPS I) is an inherited lysosomal storage disease that seriously affects the brain. Severity of neurocognitive symptoms in attenuated MPS subtype (MPS IA) broadly varies partially, due to restricted permeability of blood‐brain barrier (BBB) which limits treatment effects of intravenously applied α‐L‐iduronidase (rhIDU) enzyme. Intrathecal (IT) rhIDU application as a possible solution to circumvent BBB improved brain outcomes in canine models; therefore, our study quantifies effects of IT rhIDU on brain structure and function in an MPS IA patient with previous progressive cognitive decline. Neuropsychological testing and MRIs were performed twice prior (baseline, at 1 year) and twice after initiating IT rhIDU (at 2nd and 3rd years). The difference between pre‐ and post‐treatment means was evaluated as a percentage of the change. Neurocognitive performance improved particularly in memory tests and resulted in improved school performance after IT rhIDU treatment. White matter (WM) integrity improved together with an increase of WM and corpus callosum volumes. Hippocampal and gray matter volume decreased which may either parallel reduction of glycosaminoglycan storage or reflect typical longitudinal brain changes in early adulthood. In conclusion, our outcomes suggest neurological benefits of IT rhIDU compared to the intravenous administration on brain structure and function in a single MPS IA patient. © 2017 The Authors. American Journal of Medical Genetics Part A Published by Wiley Periodicals, Inc. … (more)
- Is Part Of:
- American journal of medical genetics. Volume 173:Issue 3(2017)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 173:Issue 3(2017)
- Issue Display:
- Volume 173, Issue 3 (2017)
- Year:
- 2017
- Volume:
- 173
- Issue:
- 3
- Issue Sort Value:
- 2017-0173-0003-0000
- Page Start:
- 780
- Page End:
- 783
- Publication Date:
- 2017-02-17
- Subjects:
- mucopolysaccharidosis -- intrathecal administration -- enzyme replacement therapy -- neuropsychology -- magnetic resonance imaging -- diffusion tensor imaging -- brain -- blood‐brain barrier
Medical genetics -- Periodicals
616.14205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.a.38073 ↗
- Languages:
- English
- ISSNs:
- 1552-4825
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.920000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 8980.xml