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Association of Biomarker Level with Cardiovascular Events: Results of a 4-Year Follow-Up Study
L Turgunova1, B Baidildina1, Y Laryushina1
1Karaganda Medical University, Karaganda, Kazakhstan.
Insights
New biomarkers, including chemokine (C-X-C motif) ligand 16 (CXCL16) and endocan, show promise in predicting cardiovascular events. These markers can help identify individuals at higher risk for developing cardiovascular disease (CVD).
Area of Science:
- Cardiology
- Biomarker Research
- Public Health
Background:
- Cardiovascular disease (CVD) poses significant public health challenges due to high morbidity and mortality rates.
- Inflammation and endothelial dysfunction are key drivers of atherosclerosis, the underlying cause of many CVDs.
- Identifying high-risk individuals through novel biomarkers is crucial for effective CVD prevention strategies.
Purpose of the Study:
- To investigate the predictive value of chemokine (C-X-C motif) ligand 16 (CXCL16), endocan, and heart-type fatty acid binding protein (H-FABP) for cardiovascular events.
- To assess the utility of these biomarkers in risk stratification for individuals without a prior history of cardiovascular events.
Main Methods:
- A cohort of 363 adults (aged 30-65) residing in Saran, Karaganda region, was recruited.
- Participants were screened and followed for 48 months (August 2014 - November 2018) to track cardiovascular events.
- Levels of CXCL16, endocan, and H-FABP were measured and analyzed for their association with event development.
Main Results:
- Biomarker levels of CXCL16, endocan, and H-FABP were significantly higher in participants who experienced cardiovascular events.
- Multivariate analysis confirmed that increased CXCL16 is associated with composite endpoint (CE) development (p < 0.001).
- Elevated endocan levels were linked to major cardiovascular events (MACE) development (p=0.008), while H-FABP showed no significant association (p=0.83).
Conclusions:
- CXCL16 and endocan are significant predictors of cardiovascular events in individuals without a prior history of CVD.
- These biomarkers may enhance risk stratification, aiding in the primary and secondary prevention of cardiovascular disease.
- Further research is warranted to explore the clinical application of CXCL16 and endocan in CVD risk assessment.
Background:
Given the high rates of morbidity and mortality from cardiovascular disease (CVD), the primary and secondary CVD prevention is one of the public health priority. Inflammation and endothelial dysfunction are the major drivers of atherosclerosis development and progression. In this regard, the study of the biomarker application as a tool to better identify high-risk individuals is an up-to-date sector of modern cardiology. The simultaneous measurement of multiple biomarkers can increase the risk stratification for people who are not known to have cardiovascular events in their history. The study aimed to investigate the predictive value of chemokine (C-X-C motif) ligand 16 (CXCL16), endocan, and heart-type fatty acid binding protein (H-FABP) in the cardiovascular event development in people who are not known to have cardiovascular events in their history.
Method:
We examined 363 people aged 30 to 65 who have been living permanently in the city of Saran, Karaganda region. The selected participants were people registered at a clinic at the city of Saran, who were screened between August and September 2014.
Results:
The follow-up period was 48 months (from August-September 2014 to November 2018). The results showed that CXCL16 (p < 0.001), endocan (p < 0.001), and H-FABP (p=0.002) biomarker levels are significantly higher in outcome groups compared with those of the no-outcome group. Univariate regression analysis proved the prognostic significance of all biomarkers in cardiovascular events development. The multivariate regression analysis after the adjustment confirmed that the CXCL16 increase was associated with the "composite endpoint" (CE) development (p < 0.001) while the endocan increased due to the development of major cardiovascular events (MACE) (p=0.008); we did not find the association of the risks of event development with the H-FABP level increase (p=0.83).
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