Evidence map›Paper›PMID 40604814›Full record

ArticleBMC veterinary research2025

Quantitative proteomics unveils potential plasma biomarkers and provides insights into the pathophysiological mechanisms underlying equine metabolic syndrome.

E M Espinosa-López, B Ortiz-Guisado, E Diez de Castro, A Durham, E Aguilera-Tejero, G Gómez-Baena

Erratum issuedAbstract read
In one paragraph

Article in BMC veterinary research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

E M Espinosa-LópezDepartment of Biochemistry and Molecular Biology, Faculty of Veterinary Sciences, University of Córdoba, Córdoba, Spain.
B Ortiz-GuisadoDepartment of Biochemistry and Molecular Biology, Faculty of Veterinary Sciences, University of Córdoba, Córdoba, Spain.
E Diez de CastroDepartment of Animal Medicine and Surgery, Faculty of Veterinary Sciences, University of Córdoba, Córdoba, Spain.
A DurhamLiphook Equine Hospital, Liphook, UK.
E Aguilera-TejeroDepartment of Animal Medicine and Surgery, Faculty of Veterinary Sciences, University of Córdoba, Córdoba, Spain.
G Gómez-BaenaDepartment of Biochemistry and Molecular Biology, Faculty of Veterinary Sciences, University of Córdoba, Córdoba, Spain. v52gobag@uco.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEquine Metabolic Syndrome (EMS) is a multifactorial endocrine disorder characterized by obesity, insulin dysregulation (ID), and an increase in the risk of laminitis, a painful condition that can lead to euthanasia in severe cases. Diagnosing EMS is challenging and often relies on clinical history including obesity, difficulty in losing weight, and recurring episodes of laminitis. The gold standard for laboratory support of an EMS diagnosis is the identification of ID, with basal insulin being the simplest and most accessible method, especially in a field setting. However, various factors such as diet, age, stress, season, medications administered, and testing protocols can influence results. Dynamic tests like the oral sugar test (OST) are preferred but present limitations due to low sensitivity and poor repeatability. These diagnostic challenges make EMS difficult to detect in veterinary medicine highlighting the need for an effective method of the early detection of EMS to prevent laminitis and its associated complications.

resultsMass spectrometry-based proteomics represents a powerful tool to identify biomarkers and explore molecular pathways related to the underlying pathology. In the current study we established an integrated proteomics pipeline to identify plasma biomarkers for EMS diagnosis. We compared plasma proteomes from healthy horses, non-ID obese horses and animals diagnosed with EMS. This comparison revealed 76 proteins with significant changes (1% FDR) between groups.

conclusionsOur study demonstrates that the complement system, the coagulation cascade and extracellular matrix remodelling pathways are altered in EMS. These findings offer new insights into the molecular basis of the development of EMS and led to the nomination of several proteins as potential biomarkers for its early detection.

Indexed as

Horse DiseasesMetabolic SyndromeAnimalsBiomarkersHorsesProteomicsBiomarkersDiagnostic biomarkersEquine metabolic syndromePlasma proteomics

Identifiers

PMID40604814
PMCPMC12217909

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.