Evidence map›Paper›PMID 38413600›Full record

Articlenpj aging2024

Accelerated elastin degradation by age-disease interaction: a common feature in age-related diseases.

Naomi Shek, Anna-Maria Choy, Chim C Lang, Bruce E Miller, Ruth Tal-Singer, Charlotte E Bolton, Neil C Thomson, James D Chalmers, Matt J Bown, David E Newby and 2 more

Open access · hybridAbstract read
In one paragraph

Article in npj aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
7.2field-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

14 citing papers in PubMed, 13 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Dermocosmetic Potential ofAntioxidants (Basel, Switzerland) · 2026
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
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

12 authors at 6 institutions in 2 countries.

Naomi ShekSystems Medicine, School of Medicine, University of Dundee, Dundee, UK.ORCID http://orcid.org/0009-0003-6532-855X
Anna-Maria ChoyMolecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, UK.ORCID http://orcid.org/0000-0002-4052-0591
Chim C LangMolecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, UK.
Bruce E MillerCOPD Foundation, Miami, USA.ORCID http://orcid.org/0000-0003-3904-3182
Ruth Tal-SingerGlobal Allergy and Airways Patient Platform, Vienna, Austria.
Charlotte E BoltonCentre for Respiratory Research, NIHR Nottingham Biomedical Research Centre, Translational Medical Sciences, School of Medicine, University of Nottingham, Nottingham, UK.
Neil C ThomsonSchool of Infection and immunity, University of Glasgow, Glasgow, Scotland, UK.
James D ChalmersMolecular and Clinical Medicine, School of Medicine, University of Dundee, Dundee, UK.
Matt J BownDepartment of Cardiovascular Sciences and NIHR Leicester Biomedical Research Centre, University of Leicester, Leicester, UK.
David E NewbyMRC / University of Edinburgh Centre for Inflammation Research, Queen's Medical Research Institute, Edinburgh, Scotland, UK.
Faisel KhanSystems Medicine, School of Medicine, University of Dundee, Dundee, UK.
Jeffrey T J HuangSystems Medicine, School of Medicine, University of Dundee, Dundee, UK. jtjhuang@dundee.ac.uk.ORCID http://orcid.org/0000-0002-6879-3014
University of Dundee · GBCOPD Foundation · USQueen's Medical Centre · GBUniversity of Glasgow · GBUniversity of Leicester · GBUniversity of Nottingham · GB

Funding

British Heart Foundation CH/09/002/26360Chief Scientist Office (CSO) CGA-17-07Heart Research UK NET21-100006Heart Research UK NET21-2302Pfizer (Pfizer Inc.) GU-022
6 · The paper itself

Abstract

Aging is a major driving force for many diseases but the relationship between chronological age, the aging process and age-related diseases is not fully understood. Fragmentation and loss of ultra-long-lived elastin are key features in aging and several age-related diseases leading to increased mortality. By comparing the relationship between age and elastin turnover with healthy volunteers, we show that accelerated elastin turnover by age-disease interaction is a common feature of age-related diseases.

Identifiers

PMID38413600
PMCPMC10899634
OpenAlexW4392199518

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.