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- Publisher Website: 10.1093/brain/awl279
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- PMID: 17071923
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Article: Proteome-based plasma biomarkers for Alzheimer's disease
Title | Proteome-based plasma biomarkers for Alzheimer's disease |
---|---|
Authors | |
Keywords | Alzheimer's disease Biomarkers Plasma Proteomics Two-dimensional gel electrophoresis (2-DGE) |
Issue Date | 2006 |
Publisher | Oxford University Press. The Journal's web site is located at http://brain.oxfordjournals.org/ |
Citation | Brain, 2006, v. 129 n. 11, p. 3042-3050 How to Cite? |
Abstract | Alzheimer's disease is a common and devastating disease for which there is no readily available biomarker to aid diagnosis or to monitor disease progression. Biomarkers have been sought in CSF but no previous study has used two-dimensional gel electrophoresis coupled with mass spectrometry to seek biomarkers in peripheral tissue. We performed a case-control study of plasma using this proteomics approach to identify proteins that differ in the disease state relative to aged controls. For discovery-phase proteomics analysis, 50 people with Alzheimer's dementia were recruited through secondary services and 50 normal elderly controls through primary care. For validation purposes a total of 511 subjects with Alzheimer's disease and other neurodegenerative diseases and normal elderly controls were examined. Image analysis of the protein distribution of the gels alone identifies disease cases with 56% sensitivity and 80% specificity. Mass spectrometric analysis of the changes observed in two-dimensional electrophoresis identified a number of proteins previously implicated in the disease pathology, including complement factor H (CFH) precursor and α-2-macroglobulin (α- 2M). Using semi-quantitative immunoblotting, the elevation of CFH and α- 2M was shown to be specific for Alzheimer's disease and to correlate with disease severity although alternative assays would be necessary to improve sensitivity and specificity. These findings suggest that blood may be a rich source for biomarkers of Alzheimer's disease and that CFH, together with other proteins such as α- 2M may be a specific markers of this illness. © 2006 The Author(s). |
Persistent Identifier | http://hdl.handle.net/10722/81482 |
ISSN | 2023 Impact Factor: 10.6 2023 SCImago Journal Rankings: 4.689 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Hye, A | en_HK |
dc.contributor.author | Lynham, S | en_HK |
dc.contributor.author | Thambisetty, M | en_HK |
dc.contributor.author | Causevic, M | en_HK |
dc.contributor.author | Campbell, J | en_HK |
dc.contributor.author | Byers, HL | en_HK |
dc.contributor.author | Hooper, C | en_HK |
dc.contributor.author | Rijsdijk, F | en_HK |
dc.contributor.author | Tabrizi, SJ | en_HK |
dc.contributor.author | Banner, S | en_HK |
dc.contributor.author | Shaw, CE | en_HK |
dc.contributor.author | Foy, C | en_HK |
dc.contributor.author | Poppe, M | en_HK |
dc.contributor.author | Archer, N | en_HK |
dc.contributor.author | Hamilton, G | en_HK |
dc.contributor.author | Powell, J | en_HK |
dc.contributor.author | Brown, RG | en_HK |
dc.contributor.author | Sham, P | en_HK |
dc.contributor.author | Ward, M | en_HK |
dc.contributor.author | Lovestone, S | en_HK |
dc.date.accessioned | 2010-09-06T08:18:18Z | - |
dc.date.available | 2010-09-06T08:18:18Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Brain, 2006, v. 129 n. 11, p. 3042-3050 | en_HK |
dc.identifier.issn | 0006-8950 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/81482 | - |
dc.description.abstract | Alzheimer's disease is a common and devastating disease for which there is no readily available biomarker to aid diagnosis or to monitor disease progression. Biomarkers have been sought in CSF but no previous study has used two-dimensional gel electrophoresis coupled with mass spectrometry to seek biomarkers in peripheral tissue. We performed a case-control study of plasma using this proteomics approach to identify proteins that differ in the disease state relative to aged controls. For discovery-phase proteomics analysis, 50 people with Alzheimer's dementia were recruited through secondary services and 50 normal elderly controls through primary care. For validation purposes a total of 511 subjects with Alzheimer's disease and other neurodegenerative diseases and normal elderly controls were examined. Image analysis of the protein distribution of the gels alone identifies disease cases with 56% sensitivity and 80% specificity. Mass spectrometric analysis of the changes observed in two-dimensional electrophoresis identified a number of proteins previously implicated in the disease pathology, including complement factor H (CFH) precursor and α-2-macroglobulin (α- 2M). Using semi-quantitative immunoblotting, the elevation of CFH and α- 2M was shown to be specific for Alzheimer's disease and to correlate with disease severity although alternative assays would be necessary to improve sensitivity and specificity. These findings suggest that blood may be a rich source for biomarkers of Alzheimer's disease and that CFH, together with other proteins such as α- 2M may be a specific markers of this illness. © 2006 The Author(s). | en_HK |
dc.language | eng | en_HK |
dc.publisher | Oxford University Press. The Journal's web site is located at http://brain.oxfordjournals.org/ | en_HK |
dc.relation.ispartof | Brain | en_HK |
dc.rights | Brain. Copyright © Oxford University Press. | en_HK |
dc.subject | Alzheimer's disease | en_HK |
dc.subject | Biomarkers | en_HK |
dc.subject | Plasma | en_HK |
dc.subject | Proteomics | en_HK |
dc.subject | Two-dimensional gel electrophoresis (2-DGE) | en_HK |
dc.title | Proteome-based plasma biomarkers for Alzheimer's disease | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0006-8950&volume=129&spage=3042&epage=3050&date=2006&atitle=Proteome-based+plasma+biomarkers+for+Alzheimer’s+disease | en_HK |
dc.identifier.email | Sham, P: pcsham@hku.hk | en_HK |
dc.identifier.authority | Sham, P=rp00459 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1093/brain/awl279 | en_HK |
dc.identifier.pmid | 17071923 | - |
dc.identifier.scopus | eid_2-s2.0-33750596715 | en_HK |
dc.identifier.hkuros | 133771 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-33750596715&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 129 | en_HK |
dc.identifier.issue | 11 | en_HK |
dc.identifier.spage | 3042 | en_HK |
dc.identifier.epage | 3050 | en_HK |
dc.identifier.isi | WOS:000241783800024 | - |
dc.publisher.place | United Kingdom | en_HK |
dc.identifier.scopusauthorid | Hye, A=6603434972 | en_HK |
dc.identifier.scopusauthorid | Lynham, S=24724971300 | en_HK |
dc.identifier.scopusauthorid | Thambisetty, M=6507073742 | en_HK |
dc.identifier.scopusauthorid | Causevic, M=6603628763 | en_HK |
dc.identifier.scopusauthorid | Campbell, J=7404875490 | en_HK |
dc.identifier.scopusauthorid | Byers, HL=7006460214 | en_HK |
dc.identifier.scopusauthorid | Hooper, C=13604722800 | en_HK |
dc.identifier.scopusauthorid | Rijsdijk, F=6701830835 | en_HK |
dc.identifier.scopusauthorid | Tabrizi, SJ=7006745684 | en_HK |
dc.identifier.scopusauthorid | Banner, S=7003546557 | en_HK |
dc.identifier.scopusauthorid | Shaw, CE=35370282000 | en_HK |
dc.identifier.scopusauthorid | Foy, C=7004396232 | en_HK |
dc.identifier.scopusauthorid | Poppe, M=15052270500 | en_HK |
dc.identifier.scopusauthorid | Archer, N=7006158241 | en_HK |
dc.identifier.scopusauthorid | Hamilton, G=7201369107 | en_HK |
dc.identifier.scopusauthorid | Powell, J=7403541196 | en_HK |
dc.identifier.scopusauthorid | Brown, RG=7406363771 | en_HK |
dc.identifier.scopusauthorid | Sham, P=34573429300 | en_HK |
dc.identifier.scopusauthorid | Ward, M=7403169022 | en_HK |
dc.identifier.scopusauthorid | Lovestone, S=7005575001 | en_HK |
dc.identifier.issnl | 0006-8950 | - |