Evidence map›Paper›PMID 37609982›Full record

ArticleJournal of the American Heart Association2023

Age-Associated Changes in Endothelial Transcriptome and Epigenetic Landscapes Correlate With Elevated Risk of Cerebral Microbleeds.

Kshitij Mohan, Gilles Gasparoni, Abdulrahman Salhab, Michael M Orlich, Robert Geffers, Steve Hoffmann, Ralf H Adams, Jörn Walter, Alfred Nordheim

Open access · goldAbstract read
In one paragraph

Article in Journal of the American Heart Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 9 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

9 authors at 5 institutions in 1 country.

Kshitij MohanInterfaculty Institute of Cell Biology University of Tübingen Tübingen Germany.ORCID 0000-0002-7978-5343
Gilles GasparoniDepartment of Genetics University of Saarland Saarbrücken Germany.ORCID 0000-0002-6423-4637
Abdulrahman SalhabDepartment of Genetics University of Saarland Saarbrücken Germany.ORCID 0000-0002-9649-6922
Michael M OrlichInterfaculty Institute of Cell Biology University of Tübingen Tübingen Germany.ORCID 0000-0001-8632-2593
Robert GeffersGenome Analytics Helmholtz Centre for Infection Research Braunschweig Germany.ORCID 0000-0003-4409-016X
Steve HoffmannLeibniz Institute on Aging Fritz Lipmann Institute Jena Germany.
Ralf H AdamsDepartment of Tissue Morphogenesis Max Planck Institute for Molecular Biomedicine Münster Germany.
Jörn WalterDepartment of Genetics University of Saarland Saarbrücken Germany.ORCID 0000-0003-0563-7417
Alfred NordheimInterfaculty Institute of Cell Biology University of Tübingen Tübingen Germany.
Saarland University · DELeibniz Institute on Aging - Fritz Lipmann Institute (FLI) · DEUniversity of Tübingen · DEHelmholtz Centre for Infection Research · DEUniversity of Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background Stroke is a leading global cause of human death and disability, with advanced aging associated with elevated incidences of stroke. Despite high mortality and morbidity of stroke, the mechanisms leading to blood-brain barrier dysfunction and development of stroke with age are poorly understood. In the vasculature of brain, endothelial cells (ECs) constitute the core component of the blood-brain barrier and provide a physical barrier composed of tight junctions, adherens junctions, and basement membrane. Methods and Results We show, in mice, the incidents of intracerebral bleeding increases with age. After isolating an enriched population of cerebral ECs from murine brains at 2, 6, 12, 18, and 24 months, we studied age-associated changes in gene expression. The study reveals age-dependent dysregulation of 1388 genes, including many involved in the maintenance of the blood-brain barrier and vascular integrity. We also investigated age-dependent changes on the levels of CpG methylation and accessible chromatin in cerebral ECs. Our study reveals correlations between age-dependent changes in chromatin structure and gene expression, whereas the dynamics of DNA methylation changes are different. Conclusions We find significant age-dependent downregulation of the

Indexed as

Endothelial CellsStrokeAnimalsApelin ReceptorsCerebral HemorrhageChromatinEpigenesis, GeneticHumansMiceTranscriptomeApelin ReceptorsChromatinagingblood‐brain barrierendothelial cellsstroke

Identifiers

PMID37609982
PMCPMC10547332
OpenAlexW4386084177

What Socratic holds

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LicenceCC BY-NC-ND
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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.