Evidence map›Paper›PMID 32049030›Full record

ArticleCell reports2020

Transcriptional Signatures of Tau and Amyloid Neuropathology.

Isabel Castanho, Tracey K Murray, Eilis Hannon, Aaron Jeffries, Emma Walker, Emma Laing, Hedley Baulf, Joshua Harvey, Lauren Bradshaw, Andrew Randall and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

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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

17 authors at 2 institutions in 1 country.

Isabel CastanhoInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Tracey K MurrayEli Lilly & Co., Erl Wood Manor, Sunninghill Road, Windlesham GU20 6PH, UK.
Eilis HannonInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Aaron JeffriesInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Emma WalkerInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Emma LaingEli Lilly & Co., Erl Wood Manor, Sunninghill Road, Windlesham GU20 6PH, UK.
Hedley BaulfInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Joshua HarveyInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Lauren BradshawEli Lilly & Co., Erl Wood Manor, Sunninghill Road, Windlesham GU20 6PH, UK.
Andrew RandallInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Karen MooreInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Paul O'NeillInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
Katie LunnonInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK.
David A CollierEli Lilly & Co., Erl Wood Manor, Sunninghill Road, Windlesham GU20 6PH, UK.
Zeshan AhmedEli Lilly & Co., Erl Wood Manor, Sunninghill Road, Windlesham GU20 6PH, UK.
Michael J O'NeillEli Lilly & Co., Erl Wood Manor, Sunninghill Road, Windlesham GU20 6PH, UK.
Jonathan MillInstitute of Biomedical and Clinical Sciences, University of Exeter Medical School, University of Exeter, Exeter EX2 5DW, UK. Electronic address: j.mill@exeter.ac.uk.
University of Exeter · GBEli Lilly (United Kingdom) · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K003240/1Medical Research Council MC_PC_14127Medical Research Council MR/M008924/1Wellcome TrustWellcome Trust WT097835MFWellcome Trust WT101650MA
6 · The paper itself

Abstract

Alzheimer's disease (AD) is associated with the intracellular aggregation of hyperphosphorylated tau and the accumulation of β-amyloid in the neocortex. We use transgenic mice harboring human tau (rTg4510) and amyloid precursor protein (J20) mutations to investigate transcriptional changes associated with the progression of tau and amyloid pathology. rTg4510 mice are characterized by widespread transcriptional differences in the entorhinal cortex with changes paralleling neuropathological burden across multiple brain regions. Differentially expressed transcripts overlap with genes identified in genetic studies of familial and sporadic AD. Systems-level analyses identify discrete co-expression networks associated with the progressive accumulation of tau that are enriched for genes and pathways previously implicated in AD pathology and overlap with co-expression networks identified in human AD cortex. Our data provide further evidence for an immune-response component in the accumulation of tau and reveal molecular pathways associated with the progression of AD neuropathology.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsDisease Models, AnimalDisease ProgressionHumansMiceMice, Transgenictau ProteinsAmyloid beta-Peptidestau ProteinsAlzheimer’s diseaseamyloidentorhinal cortexgene expressionhippocampusneuropathologyRNA-seqtautransgenic model

Identifiers

PMID32049030
PMCPMC7016505
OpenAlexW3005955078

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.