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Inflammatory Biomarkers in Heart Failure: Clinical Perspectives on hsCRP, IL-6 and Emerging Candidates
Berkan Kurt1, Konstantin Rex1, Martin Reugels1
1Department of Internal Medicine I - Cardiology, University Hospital Aachen, Aachen, Germany.
Insights
Inflammation, marked by interleukin-6 (IL-6) and high-sensitivity C-reactive protein (hsCRP), is a key driver of heart failure (HF). These biomarkers can improve risk assessment and guide personalized anti-inflammatory treatments for HF patients.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Biomarker Research
Background:
- Heart failure (HF) is a major global health concern.
- Systemic low-grade inflammation is increasingly recognized as a critical factor in HF development and progression.
- Interleukin-6 (IL-6) and high-sensitivity C-reactive protein (hsCRP) are key inflammatory markers.
Purpose of the Study:
- To review the diagnostic and therapeutic significance of IL-6 and hsCRP in HF.
- To evaluate their role in improving risk stratification and personalizing HF treatment.
- To explore their potential in precision medicine for HF.
Main Methods:
- Review of current scientific literature and clinical trial data.
- Analysis of the association between IL-6, hsCRP levels, and HF outcomes.
- Examination of evidence for IL-6's causal role in HF and coronary artery disease via Mendelian randomization studies.
Main Results:
- Elevated IL-6 and hsCRP levels are linked to higher risks of developing HF and adverse outcomes in patients with existing HF.
- While hsCRP is a downstream marker, IL-6 signaling appears causally involved in HF pathogenesis.
- Targeting inflammatory pathways is a viable therapeutic strategy for specific HF patient groups.
Conclusions:
- IL-6 and hsCRP are valuable biomarkers for assessing residual inflammatory risk in HF.
- These inflammatory markers can enhance individual risk prediction and guide anti-inflammatory therapies, advancing precision medicine in HF.
- Further large-scale studies are necessary to integrate these biomarkers into clinical HF management and guidelines.
Purpose Of Review:
Heart failure (HF) remains a leading cause of morbidity and mortality worldwide. Increasing evidence highlights that systemic low-grade inflammation is a key pathophysiological driver of HF. This review seeks to examine the diagnostic and therapeutic relevance of inflammatory biomarkers - specifically interleukin-6 (IL-6) and high-sensitivity C-reactive protein (hsCRP) - and evaluate their potential for improving risk stratification and enabling personalized treatment approaches in HF.
Recent Findings:
IL-6 and hsCRP have emerged as important markers of residual inflammatory risk in HF. Elevated levels of these biomarkers are associated with increased risk of incident HF and adverse outcomes in established disease. While hsCRP is as a downstream marker of inflammation with no causal involvement, Mendelian randomization studies support a causal role of IL-6 signaling in the development of HF and coronary artery disease. Recent and ongoing clinical trials support the concept of targeting inflammatory pathways as a therapeutic strategy in selected HF populations. Inflammatory biomarkers, particularly IL-6 and hsCRP, are promising tools for advancing precision medicine in HF by improving individual risk assessment and guiding anti-inflammatory interventions. Further large-scale studies are needed to validate the integration of inflammatory biomarkers into clinical algorithms for HF and explore their potential role in future guideline recommendations and personalized prevention strategies.
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