Evidence map›Paper›PMID 42141522›Full record

ArticleEquine veterinary journal2026

Proteomic signatures of equine dental tooth tissues in ageing and disease.

Anders Jensen, Danae Emilie Zambouli, Iris Gringel, Zoe Nugent, Kazuhiro Yamamoto, Lee Cooper, Andrew J Peffers, Guido Rocchigiani, Mandy J Peffers

Abstract read
In one paragraph

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

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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

9 authors.

Anders JensenDepartment of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Danae Emilie ZambouliDepartment of Clinical Sciences, School of Veterinary Medicine, Aristotle University of Thessaloniki, Thessaloniki, Greece.ORCID https://orcid.org/0000-0003-2839-7620
Iris GringelDepartment of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Zoe NugentDepartment of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Kazuhiro YamamotoDepartment of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.
Lee CooperInstitute of Life Course and Medical Sciences, School of Dentistry, University of Liverpool, Liverpool, UK.
Andrew J PeffersNorth Wales Equine Dental Practice, Bryn Common, Ffrith, UK.ORCID https://orcid.org/0000-0001-9096-3799
Guido RocchigianiInstitute of Infection, Veterinary and Ecological Sciences, University of Liverpool, Leahurst Campus, Neston, UK.ORCID https://orcid.org/0000-0002-3742-7636
Mandy J PeffersDepartment of Musculoskeletal and Ageing Science, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.

Funding

Dunhill Medical TrustHorse Trust G2029
6 · The paper itself

Abstract

backgroundAgeing and dental disease in horses lead to structural and functional deterioration of dental tissues, yet their molecular signatures remain poorly characterised. Understanding how these processes alter the protein composition of enamel, dentin, cementum and pulp is essential for improving equine oral health and identifying biomarkers of degeneration.

objectivesTo characterise the proteomic profiles of equine dental tissues and determine age- and disease-associated changes, with the aim of identifying proteins consistently altered across conditions. STUDY

designEx vivo proteomic study.

methodsFifteen equine cheek teeth were allocated to three groups (n = 5/group): mature adult, old and diseased. Label-free quantitative mass spectrometry was used to profile proteins across enamel, dentin, cementum and pulp. Differential abundance analysis and clustering assessed age- and disease-related effects. A Shiny-based interactive tool was developed for data exploration.

resultsA total of 1950 proteins were identified, with 58% unique to dental pulp. Ageing affected 329 proteins across all tissues, while disease impacted 379. Ageing consistently disrupted extracellular matrix (ECM) homeostasis in hard tissues. Cementum demonstrated increased catabolic markers the metalloproteinases -2 and -13. In dentin, the mineralisation protein dentin sialophosphoprotein was significantly reduced with age. Altered proteins in diseased pulp demonstrated predicted inhibition of ECM organisation (z-score = -3.05, p = 0.032) and elastic fibre formation (z-score = -2.82, p = 0.0033), while retinoic acid receptor activation was increased (z-score = 2.11, p = 0.006). Similarity analysis revealed overlapping molecular responses between ageing and disease. MAIN LIMITATIONS: Small sample size and inclusion of only cheek teeth limit generalisability. Proteomic findings require functional validation.

conclusionsAgeing and disease induce distinct yet overlapping proteomic alterations in equine dental tissues, primarily affecting ECM homeostasis. A subset of consistently altered proteins may serve as targets for regenerative strategies, with implications for improving equine dental health and welfare.

Indexed as

AgingHorse DiseasesProteomeProteomicsToothTooth DiseasesAnimalsGene Expression RegulationHorsesProteomecementumdentinenamelhorseproteomicspulp

Identifiers

PMID42141522
PMCPMC13657193

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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.