Evidence map›Paper›PMID 39851535›Full record

ReviewCells2025

Osteopontin as a Biomarker for Coronary Artery Disease.

Georgia R Layton, Ibrahim Antoun, Alice Copperwheat, Zaidhan Latif Khan, Sanjay S Bhandari, Riyaz Somani, André Ng, Mustafa Zakkar

Abstract readReview
In one paragraph

Review in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Observational
  2. Osteopontin: Its Properties, Recent Studies, and Potential Applications.International journal of molecular sciences · 2025
    Review
  3. Article
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

8 authors.

Georgia R LaytonDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UK.ORCID 0000-0002-2209-0559
Ibrahim AntounDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UK.ORCID 0000-0002-4374-7476
Alice CopperwheatDepartment of Cardiac Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UK.
Zaidhan Latif KhanUniversity of Lancaster, Bailrigg, Lancaster LA1 4YW, UK.ORCID 0009-0007-3679-143X
Sanjay S BhandariDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UK.
Riyaz SomaniDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UK.ORCID 0000-0001-5162-3644
André NgDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UK.ORCID 0000-0001-5965-0671
Mustafa ZakkarDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UK.

Funding

British Heart Foundation AA/18/3/34220British Heart Foundation CH/12/1/29419British Heart Foundation RE/24/130031British Heart Foundation RG/17/3/32,774Medical Research Council MR/S037306/1National Institute for Health Research NIHR203327
6 · The paper itself

Abstract

Osteopontin (OPN) is a sialylated phosphoprotein highly expressed in atherosclerosis and upregulated in settings of both acute and chronic inflammation. It is hypothesised that plasma levels of OPN may correlate with the presence of coronary artery disease, "CAD". This offers potential as a point-of-care testing biomarker for early diagnosis, disease monitoring, and prognosis. This review evaluates the current literature on the association between plasma OPN levels and coronary artery disease and what is currently known to support its potential as a biomarker for future practice. Electronic searches of MEDLINE and EMBASE databases were undertaken from inception until July 2024. Thirty-three studies met the inclusion criteria. All studies were observational, with gross heterogeneity in methods used to analyse the association of plasma OPN with clinical characteristics. They included case series, case-control, cross-sectional, and cohort study designs. OPN has been linked to higher cardiovascular risk and unfavourable cardiovascular outcomes. However, the evidence regarding the direct assessment of CAD severity using tools like the SYNTAX or TIMI scores, which focus on anatomical complexity and risk factors, is less definitive. This suggests that OPN may be a more precise reflection of the inflammatory processes and atherosclerotic activity contributing to unfavourable outcomes rather than a direct indicator of the anatomical severity of CAD itself. Consequently, OPN is increasingly perceived as a marker of a poor prognosis rather than a tool for assessing the severity of coronary artery lesions.

Indexed as

BiomarkersCoronary Artery DiseaseOsteopontinHumansPrognosisBiomarkersOsteopontinSPP1 protein, humanacute coronary syndromeatherosclerosiscalcificationcoronary artery bypass graftingcoronary artery diseaseosteopontin

Identifiers

PMID39851535
PMCPMC11764379

What Socratic 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 Socratic graph.