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Association of Acute-Phase IL-6 and SAA with Cardiovascular Events and Mortality Six Years After COVID-19 Infection:
Rumen Filev1,2, Boris Bogov1,2, Ralica Hadjieva1,2
1Department of Nephrology, Internal Disease Clinic, University Hospital "Saint Anna", 1750 Sofia, Bulgaria.
Insights
High inflammation markers, Interleukin-6 (IL-6) and serum amyloid A (SAA), after COVID-19 infection predict long-term cardiovascular events like heart attack and death. Early inflammation magnitude may link to future heart risks.
Area of Science:
- Cardiovascular disease research
- Infectious disease epidemiology
- Inflammatory biomarker analysis
Background:
- COVID-19 is linked to increased long-term cardiovascular risk.
- Acute inflammatory response magnitude may mediate this risk.
- Interleukin-6 (IL-6) and serum amyloid A (SAA) are key inflammatory markers.
Purpose of the Study:
- To investigate the association between post-COVID-19 IL-6 and SAA levels and major cardiovascular events.
- To assess IL-6 and SAA as potential biomarkers for post-COVID cardiovascular vulnerability.
- To analyze the relationship between acute-phase inflammatory markers and long-term cardiovascular outcomes.
Main Methods:
- Longitudinal observational study with a six-year follow-up.
- Included 97 individuals with documented SARS-CoV-2 infection.
- Measured circulating IL-6 and SAA concentrations in the acute phase.
- Composite endpoint: arrhythmia, myocardial infarction, all-cause mortality.
- Analyzed skewed biomarker data using non-parametric and penalized logistic regression.
Main Results:
- 14.4% of participants experienced a composite cardiovascular event.
- Higher IL-6 and SAA levels were significantly associated with adverse outcomes.
- IL-6 strongly predicted mortality; SAA robustly predicted composite endpoint and myocardial infarction.
- Both biomarkers independently predicted long-term adverse cardiovascular events.
Conclusions:
- Acute-phase IL-6 and SAA concentrations are associated with long-term cardiovascular outcomes after COVID-19.
- The magnitude of the acute inflammatory response may be a key factor in post-COVID cardiovascular risk.
- Combined assessment of IL-6 and SAA may offer prognostic value, requiring further validation.
Abstract:
Coronavirus disease 2019 (COVID-19) has been associated with an increased long-term cardiovascular risk, potentially mediated by magnitude of the acute inflammatory response inflammation. Interleukin-6 (IL-6) and serum amyloid A (SAA) are key components of the inflammatory cascade and may serve as biomarkers of post-COVID cardiovascular vulnerability. This longitudinal observational study investigated the association between post- COVID-19 infection IL-6 and SAA levels and major cardiovascular events over a six-year follow-up period. A total of 97 individuals with documented prior SARS-CoV-2 infection were included. Circulating IL-6 and SAA concentrations were measured in the acute phase. The composite endpoint included incident arrhythmia, myocardial infarction, and all-cause mortality. Biomarker distributions were right-skewed and were therefore analyzed using non-parametric methods and penalized logistic regression models. During follow-up, 14.4% of participants experienced the composite endpoint. Individuals with adverse outcomes had significantly higher IL-6 and SAA levels compared with event-free participants. IL-6 demonstrated the strongest association with mortality, whereas SAA showed particularly robust associations with the composite endpoint, and with myocardial infarction. Both biomarkers independently predicted long-term adverse events. Circulating IL-6 and SAA concentrations measured during the acute phase of SARS-CoV-2 infection were analyzed in relation to long-term cardiovascular outcomes. These findings support the hypothesis that the magnitude of the acute inflammatory response during SARS-CoV-2 infection may be associated with long-term cardiovascular outcomes and suggest that combined assessment of IL-6 and SAA may have potential utility for hypothesis-generating prognostic signal requiring validation, pending validation in larger studies.
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