Key result
Review outlines the complex links between inflammatory cytokines, HF subtypes, and emerging targeted therapies.
Why the study?
Inflammation contributes to heart failure progression, but relationships between inflammatory cytokines and different heart failure subtypes are complex, heterogeneous, and bidirectional.
This review summarizes the complex role of inflammatory cytokines in heart failure pathophysiology, biomarker discovery, and the potential for targeted anti-inflammatory therapies.
Should not yet change practice around inflammatory biomarkers in HF; leaves open subtype-specific immune therapies.
Inflammation plays a central role in the pathophysiology of heart failure (HF), and contributes to disease progression, morbidity and mortality. However, the relationships between inflammatory cytokines and different HF subtypes are complex, heterogeneous and bidirectional. In this review, we examine inflammatory pathways, biomarker profiles and comorbidities in HF with reduced, mildly reduced and preserved ejection fraction, and summarize evidence on the use of high-sensitivity C-reactive protein as a biomarker for systemic inflammation in HF. We provide insights into emerging methodologies for biomarker discovery in HF, and discuss the use of animal models to elucidate underlying mechanisms and test potential treatment strategies. Finally, we provide an overview of the therapeutic landscape, touching on past challenges and future opportunities for the development of targeted anti-inflammatory therapies in HF.
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Mendieta et al. (2026) conducted a review in Heart failure. Targeted anti-inflammatory therapies and inflammatory cytokines was evaluated. This review summarizes the complex relationships between inflammatory cytokines and heart failure subtypes, biomarker profiles, animal models, and emerging targeted anti-inflammatory therapies.
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