Evidence map›Paper›PMID 32179883›Full record

ArticleBrain : a journal of neurology2020

Neuroinflammation and protein aggregation co-localize across the frontotemporal dementia spectrum.

W Richard Bevan-Jones, Thomas E Cope, P Simon Jones, Sanne S Kaalund, Luca Passamonti, Kieren Allinson, Oliver Green, Young T Hong, Tim D Fryer, Robert Arnold and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
8.5field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

77 citing papers in PubMed, 110 citations in OpenAlex.

  1. Trial
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  4. Neuroinflammation and Tauopathies.Molecular biology reports · 2026
    Review
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  8. Subtracting First Principal Component May Improve 4R Tau Detectability on [Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
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17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 2 countries.

W Richard Bevan-JonesDepartment of Psychiatry, University of Cambridge, Cambridge, UK.
Thomas E CopeCambridge University Department of Clinical Neurosciences and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
P Simon JonesCambridge University Department of Clinical Neurosciences and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Sanne S KaalundCambridge University Department of Clinical Neurosciences and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Luca PassamontiCambridge University Department of Clinical Neurosciences and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Kieren AllinsonDepartment of Pathology, Cambridge University Hospitals NHS Foundation Trust, Cambridge, Cambridge, UK.
Oliver GreenIstituto di Bioimmagini e Fisiologia Molecolare (IBFM), Consiglio Nazionale delle Ricerche (CNR), via Fratelli Cervi, Milano, Italy.
Young T HongWolfson Brain Imaging Centre, University of Cambridge, Cambridge, UK.
Tim D FryerWolfson Brain Imaging Centre, University of Cambridge, Cambridge, UK.
Robert ArnoldDepartment of Psychiatry, University of Cambridge, Cambridge, UK.
Jonathan P ColesDivision of Anaesthesia, University of Cambridge, UK.
Franklin I AigbirhioWolfson Brain Imaging Centre, University of Cambridge, Cambridge, UK.
Andrew J LarnerDepartment of Neurology, The Walton Centre, Liverpool, UK.
Karalyn PattersonCambridge University Department of Clinical Neurosciences and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
John T O'BrienDepartment of Psychiatry, University of Cambridge, Cambridge, UK.
James B RoweCambridge University Department of Clinical Neurosciences and Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
University of Cambridge · GBCambridge University Hospitals NHS Foundation Trust · GBMRC Cognition and Brain Sciences Unit · GBInstitute of Molecular Bioimaging and Physiology · ITUniversity of Liverpool · GB

Funding

Medical Research Council MR/M009041/1Medical Research Council MR/M024873/1Medical Research Council MR/P01271X/1Wellcome Trust 103838
6 · The paper itself

Abstract

The clinical syndromes of frontotemporal dementia are clinically and neuropathologically heterogeneous, but processes such as neuroinflammation may be common across the disease spectrum. We investigated how neuroinflammation relates to the localization of tau and TDP-43 pathology, and to the heterogeneity of clinical disease. We used PET in vivo with (i) 11C-PK-11195, a marker of activated microglia and a proxy index of neuroinflammation; and (ii) 18F-AV-1451, a radioligand with increased binding to pathologically affected regions in tauopathies and TDP-43-related disease, and which is used as a surrogate marker of non-amyloid-β protein aggregation. We assessed 31 patients with frontotemporal dementia (10 with behavioural variant, 11 with the semantic variant and 10 with the non-fluent variant), 28 of whom underwent both 18F-AV-1451 and 11C-PK-11195 PET, and matched control subjects (14 for 18F-AV-1451 and 15 for 11C-PK-11195). We used a univariate region of interest analysis, a paired correlation analysis of the regional relationship between binding distributions of the two ligands, a principal component analysis of the spatial distributions of binding, and a multivariate analysis of the distribution of binding that explicitly controls for individual differences in ligand affinity for TDP-43 and different tau isoforms. We found significant group-wise differences in 11C-PK-11195 binding between each patient group and controls in frontotemporal regions, in both a regions-of-interest analysis and in the comparison of principal spatial components of binding. 18F-AV-1451 binding was increased in semantic variant primary progressive aphasia compared to controls in the temporal regions, and both semantic variant primary progressive aphasia and behavioural variant frontotemporal dementia differed from controls in the expression of principal spatial components of binding, across temporal and frontotemporal cortex, respectively. There was a strong positive correlation between 11C-PK-11195 and 18F-AV-1451 uptake in all disease groups, across widespread cortical regions. We confirmed this association with post-mortem quantification in 12 brains, demonstrating strong associations between the regional densities of microglia and neuropathology in FTLD-TDP (A), FTLD-TDP (C), and FTLD-Pick's. This was driven by amoeboid (activated) microglia, with no change in the density of ramified (sessile) microglia. The multivariate distribution of 11C-PK-11195 binding related better to clinical heterogeneity than did 18F-AV-1451: distinct spatial modes of neuroinflammation were associated with different frontotemporal dementia syndromes and supported accurate classification of participants. These in vivo findings indicate a close association between neuroinflammation and protein aggregation in frontotemporal dementia. The inflammatory component may be important in shaping the clinical and neuropathological patterns of the diverse clinical syndromes of frontotemporal dementia.

Indexed as

Protein AggregatesAgedCarbolinesCarbon RadioisotopesCase-Control StudiesDNA-Binding ProteinsFemaleFrontotemporal DementiaHumansInflammationIsoquinolinesMaleMicrogliaMiddle AgedPositron-Emission TomographyProtein Binding7-(6-fluoropyridin-3-yl)-5H-pyrido(4,3-b)indoleCarbolinesCarbon RadioisotopesDNA-Binding ProteinsIsoquinolinesPK 11195Protein AggregatesTARDBP protein, humanmicroglianeuropathologyprimary progressive aphasiasemantic dementiatau imaging

Identifiers

PMID32179883
PMCPMC7089669
OpenAlexW3011374615

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.