Evidence map›Paper›PMID 38451018›Full record

ArticleAging cell2024

Ercc1 DNA repair deficiency results in vascular aging characterized by VSMC phenotype switching, ECM remodeling, and an increased stress response.

Janette van der Linden, Sanne J M Stefens, José María Heredia-Genestar, Yanto Ridwan, Renata M C Brandt, Nicole van Vliet, Isa de Beer, Bibi S van Thiel, Herman Steen, Caroline Cheng and 4 more

Open access · goldAbstract read
In one paragraph

Article in Aging cell, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
6.2field-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

13 citing papers in PubMed, 19 citations in OpenAlex.

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  7. Microvascular Health as a Key Determinant of Organismal Aging.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    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

14 authors at 3 institutions in 2 countries.

Janette van der LindenDivision of Vascular Medicine and Pharmacology, Department of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands.ORCID 0009-0006-4431-9322
Sanne J M StefensDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
José María Heredia-GenestarDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Yanto RidwanDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Renata M C BrandtDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Nicole van VlietDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Isa de BeerDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Bibi S van ThielDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Herman SteenCortalix BV, Groningen, The Netherlands.
Caroline ChengDivision of Experimental Cardiology, Department of Cardiology, MC Utrecht, Utrecht, The Netherlands.
Anton J M RoksDivision of Vascular Medicine and Pharmacology, Department of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands.
A H Jan DanserDivision of Vascular Medicine and Pharmacology, Department of Internal Medicine, Erasmus University Medical Center, Rotterdam, The Netherlands.
Jeroen EssersDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Ingrid van der PluijmDepartment of Molecular Genetics, Cancer Genomics Center, Erasmus University Medical Center, Rotterdam, The Netherlands.
Erasmus MC · NLDialyse Centrum Groningen · NLUtrecht University · NL

Funding

THE IMPACT OF CELLULAR DEFENSE ON THE ROLE OF Ku80 IN GENOME MAINTENANCE AND LONGP01AG017242 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI VIJG, JAN · 1999 to 2023
$46.1M
Erasmus MC Human disease model award (HMDA) LSHM 21075Health Holland- TKI Life Sciences & Health EMCLSH 19013NIA NIH HHS P01 AG017242ZonMw project ID 733050810 (Memorabel)
6 · The paper itself

Abstract

Cardiovascular diseases are the number one cause of death globally. The most important determinant of cardiovascular health is a person's age. Aging results in structural changes and functional decline of the cardiovascular system. DNA damage is an important contributor to the aging process, and mice with a DNA repair defect caused by Ercc1 deficiency display hypertension, vascular stiffening, and loss of vasomotor control. To determine the underlying cause, we compared important hallmarks of vascular aging in aortas of both Ercc1

Indexed as

AgingDNA RepairEndonucleasesExtracellular MatrixMuscle, Smooth, VascularPhenotypeAnimalsDNA-Binding ProteinsMiceMice, Inbred C57BLMice, KnockoutMyocytes, Smooth MuscleDNA-Binding ProteinsEndonucleasesErcc1 protein, mouseagingcardiovascular diseasesErcc1vascular remodeling

Identifiers

PMID38451018
PMCPMC11113264
OpenAlexW4392551713

What OpenQuestion 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 OpenQuestion graph.