A Critical Evaluation of Inflammatory Markers in Huntington’s Disease Plasma
Author
Summary, in English
BACKGROUND: Huntington’s Disease (HD) is a hereditary, progressive neurodegenerative disorder characterised by both neurological and systemic symptoms. In HD, immune changes can be observed before the onset of overt clinical features raising the possibility that immune markers in plasma could be used to track disease progression. It has previously been demonstrated that a widespread, progressive innate immune response is detectable in plasma throughout the course of HD.
OBJECTIVE: The aim of the present study was to investigate the potential of several components of innate immunity as plasma biomarkers in HD.
METHODS: We utilised antibody-based detection technologies as well as mass spectrometric quantification, multiple reaction monitoring (MRM-MS).
RESULTS: Levels of several markers previously described as altered in HD, such as clusterin, complement component 4, complement component 9 and α-2 macroglobulin did not differ between healthy controls and HD subjects as measured by Luminex, ELISA or MRM-MS. C-reactive protein was decreased in early HD, while the other immune markers tested were unaltered.
CONCLUSIONS: Of the immune markers tested in this study, none showed potential to track with HD disease progression.
OBJECTIVE: The aim of the present study was to investigate the potential of several components of innate immunity as plasma biomarkers in HD.
METHODS: We utilised antibody-based detection technologies as well as mass spectrometric quantification, multiple reaction monitoring (MRM-MS).
RESULTS: Levels of several markers previously described as altered in HD, such as clusterin, complement component 4, complement component 9 and α-2 macroglobulin did not differ between healthy controls and HD subjects as measured by Luminex, ELISA or MRM-MS. C-reactive protein was decreased in early HD, while the other immune markers tested were unaltered.
CONCLUSIONS: Of the immune markers tested in this study, none showed potential to track with HD disease progression.
Department/s
Publishing year
2013
Language
English
Pages
125-134
Publication/Series
Journal of Huntington's disease
Volume
2
Issue
1
Document type
Journal article
Publisher
IOS Press
Topic
- Neurology
Status
Published
Research group
- Biomarkers in Brain Disease
ISBN/ISSN/Other
- ISSN: 1879-6397