Battle of the Biomarkers of Systemic Inflammation
- PMID: 40282303
- PMCID: PMC12024891
- DOI: 10.3390/biology14040438
Battle of the Biomarkers of Systemic Inflammation
Abstract
Systemic inflammation is monitored with various biomarkers; of these, C-reactive protein (CRP) is widely used due to its cost effectiveness and widespread implementation. However, its lack of specificity and delayed kinetics have directed interest in cell-free DNA (cfDNA), which offers rapid responses to cellular damage. Our review compares the use of CRP and cfDNA in myocardial infarction, sepsis, and physical exercise, focusing on their origins, kinetics, and clinical utility. cfDNA release from apoptotic or damaged cells increases within minutes to hours, providing an early marker of cellular stress. In myocardial infarction, cfDNA peaks early, indicating acute injury, while CRP rises later, reflecting prolonged inflammation. In sepsis, cfDNA correlates strongly with disease severity and prognosis, outperforming CRP in early diagnosis. During physical exercise, cfDNA offers an immediate picture of cellular stress, whereas CRP's delayed response limits its utility in this context. The interaction between CRP and cfDNA suggests their combined application could improve diagnostic accuracy and prognostic assessments. As cfDNA testing becomes more widely available, researchers will need to develop standardized protocols and determine how it can best complement CRP measurements in clinical practice. This approach offers promise for improving the management of systemic inflammation across diverse medical conditions.
Keywords: C-reactive protein (CRP); biomarkers; cell-free DNA (cfDNA); exercise; myocardial infarction; sepsis; systemic inflammation.
Conflict of interest statement
The authors declare no conflicts of interest. The funder had no role in the design of this study, data collection, analysis, decision to publish, or preparation of the manuscript.
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