Osteopontin as a Biomarker for Coronary Artery Disease
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...
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2025-01-01
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author | Georgia R. Layton Ibrahim Antoun Alice Copperwheat Zaidhan Latif Khan Sanjay S. Bhandari Riyaz Somani André Ng Mustafa Zakkar |
author_facet | Georgia R. Layton Ibrahim Antoun Alice Copperwheat Zaidhan Latif Khan Sanjay S. Bhandari Riyaz Somani André Ng Mustafa Zakkar |
author_sort | Georgia R. Layton |
collection | DOAJ |
description | 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. |
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institution | Kabale University |
issn | 2073-4409 |
language | English |
publishDate | 2025-01-01 |
publisher | MDPI AG |
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spelling | doaj-art-9dda451974ff424296bf2ed49fe85ec82025-01-24T13:26:42ZengMDPI AGCells2073-44092025-01-0114210610.3390/cells14020106Osteopontin as a Biomarker for Coronary Artery DiseaseGeorgia R. Layton0Ibrahim Antoun1Alice Copperwheat2Zaidhan Latif Khan3Sanjay S. Bhandari4Riyaz Somani5André Ng6Mustafa Zakkar7Department of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UKDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UKDepartment of Cardiac Surgery, University Hospitals of Leicester NHS Trust, Leicester LE1 5WW, UKUniversity of Lancaster, Bailrigg, Lancaster LA1 4YW, UKDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UKDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UKDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UKDepartment of Cardiovascular Sciences, University of Leicester, Leicester LE1 7RH, UKOsteopontin (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.https://www.mdpi.com/2073-4409/14/2/106coronary artery diseaseosteopontinacute coronary syndromeatherosclerosiscalcificationcoronary artery bypass grafting |
spellingShingle | Georgia R. Layton Ibrahim Antoun Alice Copperwheat Zaidhan Latif Khan Sanjay S. Bhandari Riyaz Somani André Ng Mustafa Zakkar Osteopontin as a Biomarker for Coronary Artery Disease Cells coronary artery disease osteopontin acute coronary syndrome atherosclerosis calcification coronary artery bypass grafting |
title | Osteopontin as a Biomarker for Coronary Artery Disease |
title_full | Osteopontin as a Biomarker for Coronary Artery Disease |
title_fullStr | Osteopontin as a Biomarker for Coronary Artery Disease |
title_full_unstemmed | Osteopontin as a Biomarker for Coronary Artery Disease |
title_short | Osteopontin as a Biomarker for Coronary Artery Disease |
title_sort | osteopontin as a biomarker for coronary artery disease |
topic | coronary artery disease osteopontin acute coronary syndrome atherosclerosis calcification coronary artery bypass grafting |
url | https://www.mdpi.com/2073-4409/14/2/106 |
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