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Relationship between sRAGE and eotaxin-3 with CRP in hypertensive patients at high cardiovascular risk
Colomba Falcone1, Maria Paola Buzzi, Sara Bozzini
1Interdepartmental Center of Research in Molecular Medicine, University of Pavia, Italy. colomba.falcone@unipv.it
Insights
This study found that high-sensitivity C-reactive protein (hs-CRP), soluble form of the receptor for advanced glycation end products (sRAGE), and eotaxin-3 are reliable cardiovascular risk markers. However, these markers appear to be unrelated to each other in hypertensive patients.
Area of Science:
- Biomedical research
- Cardiovascular medicine
- Nephrology
Background:
- Cardiovascular disease (CVD) is a major cause of death, particularly in patients with kidney disease.
- Chronic kidney disease and traditional risk factors exacerbate CVD risk, necessitating improved risk stratification.
- Novel biomarkers are sought to enhance cardiovascular risk assessment beyond existing scores.
Purpose of the Study:
- To investigate the relationship between novel vascular inflammation biomarkers (sRAGE and eotaxin-3) and C-reactive protein (CRP).
- To assess these biomarkers in hypertensive patients at high cardiovascular risk.
Main Methods:
- Plasma levels of soluble form of the receptor for advanced glycation end products (sRAGE), high-sensitivity C-reactive protein (hs-CRP), and eotaxin-3 were measured.
- The study included 399 hypertensive patients with diabetes mellitus, metabolic syndrome, or organ damage.
Main Results:
- No significant differences in sRAGE, eotaxin-3, or hs-CRP levels were observed between diabetic and nondiabetic subjects.
- Univariate analysis revealed no association between plasma sRAGE or eotaxin-3 levels and hs-CRP in any subgroup.
Conclusions:
- C-reactive protein (CRP) is confirmed as a significant marker of vascular inflammation.
- Soluble form of the receptor for advanced glycation end products (sRAGE) and eotaxin-3 may be involved in cardiovascular diseases.
- hs-CRP, sRAGE, and eotaxin-3 are proposed as reliable but independent cardiovascular risk markers.
Background:
Cardiovascular disease (CVD) is the leading cause of death in Western countries and is highly prevalent in patients with kidney disease. Traditional risk factors for CVD often accompany kidney dysfunction, and chronic kidney disease per se is considered an additional risk factor. Risk stratification for CVD remains suboptimal even after the introduction of global risk assessment by various scores. This has prompted the search for novel markers of cardiovascular risk, and several biomarkers have been suggested as candidates, together with C-reactive protein (CRP). The objective of the present study was to investigate the relationship between novel biomarkers of vascular inflammation (soluble form of the receptor for advanced glycation end products [sRAGE] and eotaxin-3) with CRP in a population of hypertensive patients at high cardiovascular risk.
Methods:
Plasma sRAGE, high-sensitivity CRP (hs-CRP) and eotaxin-3 were measured in 399 hypertensive patients (265 men, mean age 58 ± 8 years)with diabetes mellitus, metabolic syndrome or organ damage.
Results:
Plasma concentrations of sRAGE, eotaxin-3 and hs-CRP were not different between diabetic and nondiabetic subjects. Univariate analysis showed that plasma levels of sRAGE and eotaxin-3 were not associated with hs-CRP in either subgroup.
Conclusion:
Our study confirms the robust and widely studied role of CRP as an important marker of vascular inflammation. We also postulate the possible involvement of sRAGE and eotaxin, 2 novel biomarkers, in CVDs. On the basis of our results, we can put forward the hypotheses that hs-CRP, s-RAGE and eotaxin are reliable but unrelated cardiovascular risk markers.
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