Evidence map›Paper›PMID 42033761›Full record

ArticleCardiovascular research2026

Age-dependent dysregulation of collagen metabolism in primary cardiac fibroblasts in vitro.

Kalyani Pandya, Carlos J Alcaide-Corral, Timaeus E F Morgan, Kerry O'Rourke, Leanne M Riley, Islay Cranston, Andrew Sutherland, Mark G MacAskill, Gillian A Gray, Adriana A S Tavares

Abstract readComparative Study
In one paragraph

Article in Cardiovascular research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Kalyani PandyaCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.ORCID 0009-0002-5065-7900
Carlos J Alcaide-CorralCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
Timaeus E F MorganCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
Kerry O'RourkeCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
Leanne M RileySchool of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK.
Islay CranstonCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
Andrew SutherlandSchool of Chemistry, University of Glasgow, Glasgow G12 8QQ, UK.
Mark G MacAskillCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
Gillian A GrayCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.
Adriana A S TavaresCentre for Cardiovascular Science, The University of Edinburgh, Queens Medical Research Institute, 47 Little France Crescent, Edinburgh EH16 4TJ, UK.

Funding

British Heart Foundation FS/19/34/34354British Heart Foundation FS/4yPhD/F/20/34126British Heart Foundation RG/16/10/32375EPSRC EP/N509668/1University of Edinburgh RE/13/3/30183University of Edinburgh RG/16/10/32375
6 · The paper itself

Abstract

introductionFibroblast-driven collagen remodelling is a key process in cardiac ageing and fibrosis, yet how age and sex alter fibroblast collagen handling remains poorly characterized. This proof-of-concept study aimed to address this knowledge gap, as currently the effects of age and sex on cardiac fibroblast (cFb) collagen metabolism remain incompletely understood. METHODS AND

resultscFbs were isolated from young (4-week) and aged (18-month) Sprague-Dawley rats and cultured in vitro. Unhydroxylated (immature) and hydroxylated (mature) collagen synthesis was estimated using cis- and trans-4-[18F]fluoro-L-proline PET radiotracers as a proxy measure of collagen synthesis. Insoluble and soluble collagen deposition was assessed using colorimetric assays. No sex differences were observed in hydroxylated and hydroxylated collagen synthesis. Ageing resulted in increased hydroxylated and unhydroxylated collagen synthesis in males. Insoluble collagen deposition was higher in young males than females and decreased with ageing.

conclusionCollagen metabolism in cFbs is influenced by age, with ageing uncoupling synthesis and deposition. These findings provide preliminary mechanistic insight and intrinsic fibroblast-level differences that may underlie age- and sex-dependent cardiac remodelling.

Indexed as

AgingCollagenFibroblastsMyocardiumAge FactorsAnimalsCells, CulturedFemaleFibrosisHydroxylationMaleRats, Sprague-DawleySex FactorsCollagenAgeingCardiac fibroblastCollagenFibrosisFluoroprolineSex differences

Identifiers

PMID42033761
PMCPMC13307557

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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.