Key result
Novel biomarkers show promise for arrhythmia prediction and diagnosis but require standardization before clinical use.
Systematic Review
Novel biomarkers offer promising insights into arrhythmia mechanisms and risk prediction, but require large-scale multicenter validation and assay standardization before clinical integration.
Answers are grounded in this paper and cite their sources.
Does not support routine clinical use of novel biomarkers; leaves open their validated role in arrhythmia risk prediction.
Arrhythmia is an important cause of cardiovascular disease deaths and a serious threat to human health, but the current means of identification are limited. Biomarkers, with the advantages of easy access and rapid detection, have shown significant value in arrhythmia risk prediction, precision diagnosis, and prognosis assessment. In recent years, with the development of molecular biology and multiomics technology, some novel biomarkers have made great breakthroughs in revealing the pathological mechanisms of arrhythmia. However, clinical translation still faces challenges such as a lack of standardization of assays and insufficient clinical prospective validation. This review comprehensively searched studies published between 2010 and 2025 in PubMed, Web of Science, Embase, and CENTRAL databases, focusing on the mechanisms underlying the role of arrhythmia biomarkers in inflammation, fibrosis, autoimmunity, and electrical remodeling and clinical translation potential. Future research should focus on the combined application of multiple biomarkers and the discovery of subtype‐specific markers. Conducting large‐scale, multicenter studies to validate these biomarkers and ultimately integrate them into clinical practice is crucial for advancing biomarker‐guided individualized antiarrhythmic therapy.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2026) conducted a systematic review in Arrhythmia. Novel biomarkers was evaluated on Mechanisms underlying the role of arrhythmia biomarkers in inflammation, fibrosis, autoimmunity, and electrical remodeling and clinical translation potential. Novel biomarkers reveal pathological mechanisms of arrhythmia in inflammation, fibrosis, autoimmunity, and electrical remodeling, but require large-scale multicenter validation for clinical use.
Synapse has enriched 10 related papers. Consider them for comparative context: