Disease stage determines the efficacy of treatment of a paediatric neurodegenerative disease. (10th April 2014)
- Record Type:
- Journal Article
- Title:
- Disease stage determines the efficacy of treatment of a paediatric neurodegenerative disease. (10th April 2014)
- Main Title:
- Disease stage determines the efficacy of treatment of a paediatric neurodegenerative disease
- Authors:
- Hassiotis, Sofia
Beard, Helen
Luck, Amanda
Trim, Paul J.
King, Barbara
Snel, Marten F.
Hopwood, John J.
Hemsley, Kim M. - Abstract:
- <abstract abstract-type="main" id="ejn12557-abs-0001"> <title>Abstract</title> <p>Lysosomal storage disorders are a large group of inherited metabolic conditions resulting from the deficiency of proteins involved in lysosomal catabolism, with resulting accumulation of substrates inside the cell. Two‐thirds of these disorders are associated with a neurodegenerative phenotype and, although few therapeutic options are available to patients at present, clinical trials of several treatments including lysosomal enzyme replacement are underway. Although animal studies indicate the efficacy of pre‐symptomatic treatment, it is largely unknown whether symptomatic disease‐related pathology and functional deficits are reversible. To begin to address this, we used a naturally‐occurring mouse model with Sanfilippo syndrome (mucopolysaccharidosis type IIIA) to examine the effectiveness of intracisternal cerebrospinal fluid enzyme replacement in early, mid‐ and symptomatic disease stage mice. We observed a disease‐stage‐dependent treatment effect, with the most significant reductions in primary and secondary substrate accumulation, astrogliosis and protein aggregate accumulation seen in mucopolysaccharidosis type IIIA mice treated very early in the disease course. Affected mice treated at a symptomatic age exhibited little change in these neuropathological markers in the time‐frame of the study. Microgliosis was refractory to treatment regardless of the age at which treatment was<abstract abstract-type="main" id="ejn12557-abs-0001"> <title>Abstract</title> <p>Lysosomal storage disorders are a large group of inherited metabolic conditions resulting from the deficiency of proteins involved in lysosomal catabolism, with resulting accumulation of substrates inside the cell. Two‐thirds of these disorders are associated with a neurodegenerative phenotype and, although few therapeutic options are available to patients at present, clinical trials of several treatments including lysosomal enzyme replacement are underway. Although animal studies indicate the efficacy of pre‐symptomatic treatment, it is largely unknown whether symptomatic disease‐related pathology and functional deficits are reversible. To begin to address this, we used a naturally‐occurring mouse model with Sanfilippo syndrome (mucopolysaccharidosis type IIIA) to examine the effectiveness of intracisternal cerebrospinal fluid enzyme replacement in early, mid‐ and symptomatic disease stage mice. We observed a disease‐stage‐dependent treatment effect, with the most significant reductions in primary and secondary substrate accumulation, astrogliosis and protein aggregate accumulation seen in mucopolysaccharidosis type IIIA mice treated very early in the disease course. Affected mice treated at a symptomatic age exhibited little change in these neuropathological markers in the time‐frame of the study. Microgliosis was refractory to treatment regardless of the age at which treatment was instigated. Although longer‐term studies are warranted, these findings indicate the importance of early intervention in this condition.</p> </abstract> … (more)
- Is Part Of:
- European journal of neuroscience. Volume 39:Number 12(2014:Jun.)
- Journal:
- European journal of neuroscience
- Issue:
- Volume 39:Number 12(2014:Jun.)
- Issue Display:
- Volume 39, Issue 12 (2014)
- Year:
- 2014
- Volume:
- 39
- Issue:
- 12
- Issue Sort Value:
- 2014-0039-0012-0000
- Page Start:
- 2139
- Page End:
- 2150
- Publication Date:
- 2014-04-10
- Subjects:
- Nervous system -- Periodicals
612.8 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1460-9568 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ejn.12557 ↗
- Languages:
- English
- ISSNs:
- 0953-816X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3829.731700
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3832.xml