Evidence map›Paper›PMID 25077967›Full record

ArticleThe Journal of biological chemistry2014

Proteomic analysis reveals age-related changes in tendon matrix composition, with age- and injury-specific matrix fragmentation.

Mandy J Peffers, Chavaunne T Thorpe, John A Collins, Robin Eong, Timothy K J Wei, Hazel R C Screen, Peter D Clegg

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
8.0field-weighted citation impact, top 2% 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

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Epigenetic mechanisms in Tendon Ageing.British medical bulletin · 2020
    Pooled it
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  14. Depletion ofInternational journal of molecular sciences · 2023
    Article
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  16. Presbyphagia: Dysphagia in the elderly.World journal of clinical cases · 2023
    Review
  17. Article
  18. 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

7 authors at 2 institutions in 2 countries.

Mandy J PeffersFrom the Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, Leahurst Campus, Neston CH64 7TE.
Chavaunne T ThorpeFrom the Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, Leahurst Campus, Neston CH64 7TE, Institute of Bioengineering, Queen Mary University of London, Mile End Road, London E1 4NS, and c.thorpe@qmul.ac.uk.
John A CollinsFrom the Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, Leahurst Campus, Neston CH64 7TE.
Robin EongFrom the Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, Leahurst Campus, Neston CH64 7TE, School of Life Sciences, Ngee Ann Polytechnic, Singapore 599489.
Timothy K J WeiFrom the Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, Leahurst Campus, Neston CH64 7TE, School of Life Sciences, Ngee Ann Polytechnic, Singapore 599489.
Hazel R C ScreenInstitute of Bioengineering, Queen Mary University of London, Mile End Road, London E1 4NS, and.
Peter D CleggFrom the Department of Musculoskeletal Biology, Institute of Ageing and Chronic Disease, University of Liverpool, Leahurst Campus, Neston CH64 7TE.
University of Liverpool · GBQueen Mary University of London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/K008412/1Medical Research Council MR/K006312/1Wellcome Trust WT088557MA
6 · The paper itself

Abstract

Energy storing tendons, such as the human Achilles and equine superficial digital flexor tendon (SDFT), are highly prone to injury, the incidence of which increases with aging. The cellular and molecular mechanisms that result in increased injury in aged tendons are not well established but are thought to result in altered matrix turnover. However, little attempt has been made to fully characterize the tendon proteome nor determine how the abundance of specific tendon proteins changes with aging and/or injury. The aim of this study was, therefore, to assess the protein profile of normal SDFTs from young and old horses using label-free relative quantification to identify differentially abundant proteins and peptide fragments between age groups. The protein profile of injured SDFTs from young and old horses was also assessed. The results demonstrate distinct proteomic profiles in young and old tendon, with alterations in the levels of proteins involved in matrix organization and regulation of cell tension. Furthermore, we identified several new peptide fragments (neopeptides) present in aged tendons, suggesting that there are age-specific cleavage patterns within the SDFT. Proteomic profile also differed between young and old injured tendon, with a greater number of neopeptides identified in young injured tendon. This study has increased the knowledge of molecular events associated with tendon aging and injury, suggesting that maintenance and repair of tendon tissue may be reduced in aged individuals and may help to explain why the risk of injury increases with aging.

Indexed as

ProteomicsAge FactorsAgingAnimalsElectrophoresis, Polyacrylamide GelExtracellular MatrixHorsesHumansTendon InjuriesTendonsAgingCollagenDiseaseEquineFibromodulinMass Spectrometry (MS)NeopeptideProtein DegradationProteoglycan

Identifiers

PMID25077967
PMCPMC4162187
OpenAlexW2062749480

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.