4.2 Article

Alpha- and gamma-synuclein proteins are present in cerebrospinal fluid and are increased in aged subjects with neurodegenerative and vascular changes

Journal

DEMENTIA AND GERIATRIC COGNITIVE DISORDERS
Volume 26, Issue 1, Pages 32-42

Publisher

KARGER
DOI: 10.1159/000141039

Keywords

alpha-synuclein; gamma-synuclein; cerebrospinal fluid; neurodegeneration; lewy body disease; Alzheimer's disease; vascular dementia

Funding

  1. MRC [G0502157, G9901400, G0400074] Funding Source: UKRI
  2. Medical Research Council [G0400074, G0502157, G9901400] Funding Source: Medline

Ask authors/readers for more resources

Background: Disease-specific biomarkers should reflect a fundamental feature of neuropathology and be validated in neuropathologically confirmed cases. Several synaptic proteins have been described in cerebrospinal fluid (CSF) of patients with dementia. In Lewy body disease alpha-synuclein is incorporated within Lewy bodies and alpha-, beta- and gamma-synucleins in dystrophic neuritis. These pathological changes are expected to be seen in CSF. Methods: A total of 25 CSF postmortem samples (8 control and 17 subjects with dementia) were used to quantify alpha- and gamma-synucleins and IgG. Results: We describe for the first time the presence of alpha-synuclein in CSF. There is an elevation of both alpha- and gamma-synucleins in CSF from elderly individuals with Alzheimer's disease, Lewy body disease (LBD) and vascular dementia (CVD), compared to normal controls. gamma-Synuclein showed a greater elevation in LBD, IgG in CVD. The elevation of alpha- and beta-synucleins was seen from Braak stage III onwards and remained stable until Braak stage VI. These results were not influenced by age at death or post-mortem delay. Conclusions: The reported increases in alpha- and gamma-synucleins and IgG in the ventricular CSF of individuals with dementia are novel findings. They now need to be explored further using a greater number of cases in each subgroup, using lumbar CSF samples to determine their applicability and relevance to a clinical diagnostic setting. It needs to be established whether using these markers may help to discriminate LBD from other types of neurodegenerative and vascular dementias. Copyright (c) 2008 S. Karger AG, Basel.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available