Evidence map›Paper›PMID 33694209›Full record

ArticleGlia2021

The pro-inflammatory microRNA miR-155 influences fibrillar β-Amyloid

Macarena S Aloi, Katherine E Prater, Bryce Sopher, Stephanie Davidson, Suman Jayadev, Gwenn A Garden

Open access · greenAbstract read
In one paragraph

Article in Glia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
5.2field-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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 49 citations in OpenAlex.

  1. Pooled it
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  12. Alzheimer's disease-induced phagocytic microglia express a specific profile of coding and non-coding RNAs.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Article
  13. Non-coding RNAs and neuroinflammation: implications for neurological disorders.Experimental biology and medicine (Maywood, N.J.) · 2024
    Review
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  16. A state-of-the-art review on miRNA in prevention and treatment of AlzheimerZhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2023
    Review
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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

6 authors at 2 institutions in 1 country.

Macarena S AloiDepartment of Pathology, School of Medicine, University of Washington, Seattle, Washington, USA.ORCID 0000-0001-8235-1231
Katherine E PraterDepartment of Neurology, School of Medicine, University of Washington, Seattle, Washington, USA.ORCID 0000-0001-8615-207X
Bryce SopherDepartment of Neurology, School of Medicine, University of Washington, Seattle, Washington, USA.
Stephanie DavidsonDepartment of Neurology, School of Medicine, University of Washington, Seattle, Washington, USA.
Suman JayadevDepartment of Neurology, School of Medicine, University of Washington, Seattle, Washington, USA.ORCID 0000-0003-3164-9665
Gwenn A GardenDepartment of Pathology, School of Medicine, University of Washington, Seattle, Washington, USA.ORCID 0000-0002-8753-6515
University of Washington · USBaylor College of Medicine · US

Funding

Neurobehavior, Neuropathology, and Risk Factors in Alzheimer's DiseaseT32AG052354 · NIA · UNIVERSITY OF WASHINGTON · PI Brian C. Kraemer, ELAINE R. PESKIND · 2016 to 2026
$6.7M
MicroRNA regulation of central nervous system and systemic inflammation in ADRF1AG051437 · NIA · UNIVERSITY OF WASHINGTON · PI GARDEN, GWENN A, JAYADEV, SUMAN · 2015 to 2019
$2.6M
Molecular Regulation of Microglia BehaviorR01NS073848 · NINDS · UNIVERSITY OF WASHINGTON · PI GARDEN, GWENN A · 2011 to 2016
$1.7M
Molecular Medicine Training ProgramT32GM095421 · NIGMS · UNIVERSITY OF WASHINGTON · PI HAWN, THOMAS R, LILES, W. CONRAD · 2011 to 2020
$1.6M
Howard Hughes Medical InstituteNIA NIH HHS RF1 AG051437NIA NIH HHS T32 AG052354NIGMS NIH HHS T32 GM095421NINDS NIH HHS R01 NS073848
6 · The paper itself

Abstract

Microglia are the innate immune cells of the central nervous system that adopt rapid functional changes in response to Damage Associated Molecular Patterns, including aggregated β-Amyloid (Aβ) found in Alzheimer's disease (AD). microRNAs (miRNAs) are post-transcriptional modulators that influence the timing and magnitude of microglia inflammatory responses by downregulating the expression of inflammatory effectors. Recent studies implicate miR-155, a miRNA known to regulate inflammatory responses, in the pathogenesis of neurodegenerative disorders including multiple sclerosis, ALS, familial Parkinson's disease, and AD. In this work, we asked if miR-155 expression in microglia modifies cellular behaviors in response to fibrillar Aβ

Indexed as

Alzheimer DiseaseMicroRNAsAmyloid beta-PeptidesHumansLipopolysaccharidesMicrogliaAmyloid beta-PeptidesLipopolysaccharidesMicroRNAsMIRN155 microRNA, humancatabolismfibrillar Aβ1-42miR-146amiR-155miRNAsprimary microglia

Identifiers

PMID33694209
PMCPMC9098129
OpenAlexW3135533676

What OpenQuestion holds

Textmetadata
LicenceTDM
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 OpenQuestion graph.