TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration
Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer’s disease (AD) harbour TDP-43 immunoreactive pathological changes in their brains. Using ELISA, we investigated whether we could detect the presence, or increased am...
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Published in | Acta neuropathologica Vol. 116; no. 2; pp. 141 - 146 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer-Verlag
01.08.2008
Springer Nature B.V |
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Abstract | Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer’s disease (AD) harbour TDP-43 immunoreactive pathological changes in their brains. Using ELISA, we investigated whether we could detect the presence, or increased amounts, of TDP-43 in plasma of patients with FTLD and AD compared to normal control subjects. We detected elevated levels of TDP-43 protein in plasma of 46% patients with FTLD with clinical frontotemporal dementia (FTD) and 22% patients with AD, compared to 8% of control subjects. The proportions of patients with FTD and AD showing raised plasma TDP-43 levels correspond closely to those proportions known from autopsy studies to contain TDP-43 pathological changes in their brains. Raised TDP-43 plasma levels may thereby index TDP-43 pathology within the brain. Plasma TDP-43 levels may be a biomarker that can provide a laboratory test capable of identifying the presence of TDP-43 brain pathology in neurodegenerative disease during life. It may help to distinguish those cases of FTLD with ubiquitin/TDP-43 pathology in their brains from those with tauopathy. As a predictive test, plasma TDP-43 level may have great practical value in directing therapeutic strategies aimed at preventing or removing tau or TDP-43 pathological changes from the brain in FTLD and AD. |
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AbstractList | Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer's disease (AD) harbour TDP-43 immunoreactive pathological changes in their brains. Using ELISA, we investigated whether we could detect the presence, or increased amounts, of TDP-43 in plasma of patients with FTLD and AD compared to normal control subjects. We detected elevated levels of TDP-43 protein in plasma of 46% patients with FTLD with clinical frontotemporal dementia (FTD) and 22% patients with AD, compared to 8% of control subjects. The proportions of patients with FTD and AD showing raised plasma TDP-43 levels correspond closely to those proportions known from autopsy studies to contain TDP-43 pathological changes in their brains. Raised TDP-43 plasma levels may thereby index TDP-43 pathology within the brain. Plasma TDP-43 levels may be a biomarker that can provide a laboratory test capable of identifying the presence of TDP-43 brain pathology in neurodegenerative disease during life. It may help to distinguish those cases of FTLD with ubiquitin/TDP-43 pathology in their brains from those with tauopathy. As a predictive test, plasma TDP-43 level may have great practical value in directing therapeutic strategies aimed at preventing or removing tau or TDP-43 pathological changes from the brain in FTLD and AD.Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer's disease (AD) harbour TDP-43 immunoreactive pathological changes in their brains. Using ELISA, we investigated whether we could detect the presence, or increased amounts, of TDP-43 in plasma of patients with FTLD and AD compared to normal control subjects. We detected elevated levels of TDP-43 protein in plasma of 46% patients with FTLD with clinical frontotemporal dementia (FTD) and 22% patients with AD, compared to 8% of control subjects. The proportions of patients with FTD and AD showing raised plasma TDP-43 levels correspond closely to those proportions known from autopsy studies to contain TDP-43 pathological changes in their brains. Raised TDP-43 plasma levels may thereby index TDP-43 pathology within the brain. Plasma TDP-43 levels may be a biomarker that can provide a laboratory test capable of identifying the presence of TDP-43 brain pathology in neurodegenerative disease during life. It may help to distinguish those cases of FTLD with ubiquitin/TDP-43 pathology in their brains from those with tauopathy. As a predictive test, plasma TDP-43 level may have great practical value in directing therapeutic strategies aimed at preventing or removing tau or TDP-43 pathological changes from the brain in FTLD and AD. Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer’s disease (AD) harbour TDP-43 immunoreactive pathological changes in their brains. Using ELISA, we investigated whether we could detect the presence, or increased amounts, of TDP-43 in plasma of patients with FTLD and AD compared to normal control subjects. We detected elevated levels of TDP-43 protein in plasma of 46% patients with FTLD with clinical frontotemporal dementia (FTD) and 22% patients with AD, compared to 8% of control subjects. The proportions of patients with FTD and AD showing raised plasma TDP-43 levels correspond closely to those proportions known from autopsy studies to contain TDP-43 pathological changes in their brains. Raised TDP-43 plasma levels may thereby index TDP-43 pathology within the brain. Plasma TDP-43 levels may be a biomarker that can provide a laboratory test capable of identifying the presence of TDP-43 brain pathology in neurodegenerative disease during life. It may help to distinguish those cases of FTLD with ubiquitin/TDP-43 pathology in their brains from those with tauopathy. As a predictive test, plasma TDP-43 level may have great practical value in directing therapeutic strategies aimed at preventing or removing tau or TDP-43 pathological changes from the brain in FTLD and AD. Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer's disease (AD) harbour TDP-43 immunoreactive pathological changes in their brains. Using ELISA, we investigated whether we could detect the presence, or increased amounts, of TDP-43 in plasma of patients with FTLD and AD compared to normal control subjects. We detected elevated levels of TDP-43 protein in plasma of 46% patients with FTLD with clinical frontotemporal dementia (FTD) and 22% patients with AD, compared to 8% of control subjects. The proportions of patients with FTD and AD showing raised plasma TDP-43 levels correspond closely to those proportions known from autopsy studies to contain TDP-43 pathological changes in their brains. Raised TDP-43 plasma levels may thereby index TDP-43 pathology within the brain. Plasma TDP-43 levels may be a biomarker that can provide a laboratory test capable of identifying the presence of TDP-43 brain pathology in neurodegenerative disease during life. It may help to distinguish those cases of FTLD with ubiquitin/TDP-43 pathology in their brains from those with tauopathy. As a predictive test, plasma TDP-43 level may have great practical value in directing therapeutic strategies aimed at preventing or removing tau or TDP-43 pathological changes from the brain in FTLD and AD. [PUBLICATION ABSTRACT] |
Author | Neary, David Foulds, Penelope Allsop, David Snowden, Julie S. Mann, David M. A. McAuley, Erica Gibbons, Linda Pickering-Brown, Stuart M. Davidson, Yvonne |
Author_xml | – sequence: 1 givenname: Penelope surname: Foulds fullname: Foulds, Penelope organization: Division of Biomedical and Life Sciences, School of Health and Medicine, University of Lancaster – sequence: 2 givenname: Erica surname: McAuley fullname: McAuley, Erica organization: Division of Biomedical and Life Sciences, School of Health and Medicine, University of Lancaster – sequence: 3 givenname: Linda surname: Gibbons fullname: Gibbons, Linda organization: Clinical Neurosciences Research Group, School of Translational Medicine, Faculty of Medical and Human Sciences, University of Manchester, Greater Manchester Neurosciences Centre, Hope Hospital – sequence: 4 givenname: Yvonne surname: Davidson fullname: Davidson, Yvonne organization: Clinical Neurosciences Research Group, School of Translational Medicine, Faculty of Medical and Human Sciences, University of Manchester, Greater Manchester Neurosciences Centre, Hope Hospital – sequence: 5 givenname: Stuart M. surname: Pickering-Brown fullname: Pickering-Brown, Stuart M. organization: Clinical Neurosciences Research Group, School of Translational Medicine, Faculty of Medical and Human Sciences, University of Manchester – sequence: 6 givenname: David surname: Neary fullname: Neary, David organization: Clinical Neurosciences Research Group, School of Translational Medicine, Faculty of Medical and Human Sciences, University of Manchester, Greater Manchester Neurosciences Centre, Hope Hospital – sequence: 7 givenname: Julie S. surname: Snowden fullname: Snowden, Julie S. organization: Clinical Neurosciences Research Group, School of Translational Medicine, Faculty of Medical and Human Sciences, University of Manchester, Greater Manchester Neurosciences Centre, Hope Hospital – sequence: 8 givenname: David surname: Allsop fullname: Allsop, David organization: Division of Biomedical and Life Sciences, School of Health and Medicine, University of Lancaster – sequence: 9 givenname: David M. A. surname: Mann fullname: Mann, David M. A. email: david.mann@manchester.ac.uk organization: Clinical Neurosciences Research Group, School of Translational Medicine, Faculty of Medical and Human Sciences, University of Manchester, Greater Manchester Neurosciences Centre, Hope Hospital |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/18506455$$D View this record in MEDLINE/PubMed |
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Keywords | Plasma Frontotemporal lobar degeneration Biomarker Alzheimer’s disease TDP-43 |
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PublicationDecade | 2000 |
PublicationPlace | Berlin/Heidelberg |
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PublicationTitle | Acta neuropathologica |
PublicationTitleAbbrev | Acta Neuropathol |
PublicationTitleAlternate | Acta Neuropathol |
PublicationYear | 2008 |
Publisher | Springer-Verlag Springer Nature B.V |
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The Tajiri project publication-title: Alzheimer Dis Assoc Disord doi: 10.1097/00002093-200401000-00002 – volume: 171 start-page: 227 year: 2007 end-page: 240 ident: CR7 article-title: TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions publication-title: Am J Pathol doi: 10.2353/ajpath.2007.070182 – volume: 314 start-page: 130 year: 2006 end-page: 133 ident: CR24 article-title: Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis publication-title: Science doi: 10.1126/science.1134108 – volume: 129 start-page: 3091 year: 2006 ident: 389_CR28 publication-title: Brain doi: 10.1093/brain/awl267 – volume: 442 start-page: 916 year: 2006 ident: 389_CR3 publication-title: Nature doi: 10.1038/nature05016 – volume: 113 start-page: 535 year: 2007 ident: 389_CR29 publication-title: Acta Neuropathol doi: 10.1007/s00401-007-0206-9 – volume: 74 start-page: 1322 year: 2004 ident: 389_CR5 publication-title: Am J Hum Genet doi: 10.1086/420978 – volume: 110 start-page: 501 year: 2005 ident: 389_CR27 publication-title: Acta Neuropathol doi: 10.1007/s00401-005-1079-4 – volume: 129 start-page: 3103 year: 2006 ident: 389_CR4 publication-title: Brain doi: 10.1093/brain/awl268 – volume: 61 start-page: 427 year: 2007 ident: 389_CR17 publication-title: Ann Neurol doi: 10.1002/ana.21147 – volume: 113 start-page: 521 year: 2007 ident: 389_CR9 publication-title: Acta Neuropathol doi: 10.1007/s00401-006-0189-y – volume: 171 start-page: 227 year: 2007 ident: 389_CR7 publication-title: Am J Pathol doi: 10.2353/ajpath.2007.070182 – volume: 442 start-page: 920 year: 2006 ident: 389_CR8 publication-title: Nature doi: 10.1038/nature05017 – volume: 61 start-page: 435 year: 2007 ident: 389_CR1 publication-title: Ann Neurol doi: 10.1002/ana.21154 – volume: 83 start-page: 130 year: 2004 ident: 389_CR30 publication-title: Genomics doi: 10.1016/S0888-7543(03)00214-3 – volume: 129 start-page: 3124 year: 2006 ident: 389_CR26 publication-title: Brain doi: 10.1093/brain/awl289 – volume: 351 start-page: 602 year: 2006 ident: 389_CR2 publication-title: Biochem Biophys Res Commun doi: 10.1016/j.bbrc.2006.10.093 – volume: 34 start-page: 939 year: 1984 ident: 389_CR18 publication-title: Neurology doi: 10.1212/WNL.34.7.939 – volume: 314 start-page: 130 year: 2006 ident: 389_CR24 publication-title: Science doi: 10.1126/science.1134108 – volume: 59 start-page: 952 year: 2006 ident: 389_CR10 publication-title: Ann Neurol doi: 10.1002/ana.20873 – volume: 4 start-page: 771 year: 2005 ident: 389_CR23 publication-title: Lancet Neurol doi: 10.1016/S1474-4422(05)70223-4 – volume: 130 start-page: 1386 year: 2007 ident: 389_CR12 publication-title: Brain doi: 10.1093/brain/awm065 – volume: 8 start-page: 14 year: 2003 ident: 389_CR25 publication-title: Mol Psychiatry doi: 10.1038/sj.mp.4001239 – volume: 63 start-page: 115 year: 2004 ident: 389_CR11 publication-title: Neurology doi: 10.1212/01.WNL.0000132523.27540.81 – volume: 18 start-page: 3 year: 2004 ident: 389_CR19 publication-title: Alzheimer Dis Assoc Disord doi: 10.1097/00002093-200401000-00002 – volume: 114 start-page: 5 year: 2007 ident: 389_CR6 publication-title: Acta Neuropathol doi: 10.1007/s00401-007-0237-2 – volume: 108 start-page: 379 year: 2005 ident: 389_CR14 publication-title: Acta Neuropathol doi: 10.1007/s00401-004-0900-9 – volume: 51 start-page: 1546 year: 1998 ident: 389_CR22 publication-title: Neurology doi: 10.1212/WNL.51.6.1546 – volume: 106 start-page: 148 year: 2002 ident: 389_CR13 publication-title: Acta Neurol Scand doi: 10.1034/j.1600-0404.2002.01225.x – volume: 64 start-page: 420 year: 2005 ident: 389_CR20 publication-title: J Neuropathol Exp Neurol doi: 10.1093/jnen/64.5.420 – volume: 129 start-page: 3081 year: 2006 ident: 389_CR16 publication-title: Brain doi: 10.1093/brain/awl271 – volume: 112 start-page: 539 year: 2006 ident: 389_CR15 publication-title: Acta Neuropathol doi: 10.1007/s00401-006-0138-9 – volume: 114 start-page: 221 year: 2007 ident: 389_CR21 publication-title: Acta Neuropathol doi: 10.1007/s00401-007-0261-2 |
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Snippet | Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer’s disease (AD) harbour... Autopsy studies have shown that about 55% of patients with frontotemporal lobar degeneration (FTLD) and 25% of patients with Alzheimer's disease (AD) harbour... |
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SubjectTerms | Adult Aged Alzheimer Disease - blood Alzheimer Disease - metabolism Alzheimer Disease - pathology Alzheimer's disease Autopsies Biomarkers Biomarkers - blood Brain - metabolism Brain - pathology Brain research Dementia Dementia - blood Dementia - metabolism Dementia - pathology Disease DNA-Binding Proteins - blood Enzyme-Linked Immunosorbent Assay Female Histology Humans Immunoprecipitation Male Medicine Medicine & Public Health Middle Aged Mutation Neurosciences Original Paper Pathology Plasma Proteins |
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Title | TDP-43 protein in plasma may index TDP-43 brain pathology in Alzheimer’s disease and frontotemporal lobar degeneration |
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