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 inActa neuropathologica Vol. 116; no. 2; pp. 141 - 146
Main Authors Foulds, Penelope, McAuley, Erica, Gibbons, Linda, Davidson, Yvonne, Pickering-Brown, Stuart M., Neary, David, Snowden, Julie S., Allsop, David, Mann, David M. A.
Format Journal Article
LanguageEnglish
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.
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
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  organization: Division of Biomedical and Life Sciences, School of Health and Medicine, University of Lancaster
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  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.
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  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
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  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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Issue 2
Keywords Plasma
Frontotemporal lobar degeneration
Biomarker
Alzheimer’s disease
TDP-43
Language English
License This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
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PublicationTitle Acta neuropathologica
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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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proquest
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springer
SourceType Open Access Repository
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Enrichment Source
Publisher
StartPage 141
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
URI https://link.springer.com/article/10.1007/s00401-008-0389-8
https://www.ncbi.nlm.nih.gov/pubmed/18506455
https://www.proquest.com/docview/211858507
https://www.proquest.com/docview/19480133
https://www.proquest.com/docview/69320333
https://pubmed.ncbi.nlm.nih.gov/PMC2464623
Volume 116
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