# Epigenetic Liquid Biopsy Marks Atrial Fibrillation: Evidence from the AF Big Picture Study

**Authors:** Riccardo Proietti, Nicola Tidbury, Joshua Preston, Maanya Vittal, Philippa McCabe, Garry McDowell, Gregory Y. H. Lip, Manlio Vinciguerra

PMC · DOI: 10.3390/epigenomes10010009 · Epigenomes · 2026-02-05

## TL;DR

This study explores whether blood levels of histone complexes can help diagnose and better understand atrial fibrillation, a common heart condition.

## Contribution

The study is the first to investigate circulating histone levels as potential biomarkers for atrial fibrillation.

## Key findings

- AF patients had higher levels of H2A/H2B and H3/H4 histone dimers compared to controls.
- H2A/H2B levels were elevated in AF patients regardless of gender, smoking, diabetes, or medication.
- An inverse correlation between H2A and BMI was observed in the overall population.

## Abstract

Background/Objectives: Atrial fibrillation (AF) is currently the most common arrhythmia worldwide, and it is linked to increased mortality and morbidity, hence the need for a better clinical stratification of AF patients. Histone complexes or nucleosomes, released into the blood circulation, are found elevated in acute conditions such as stroke, trauma, and sepsis. The aim of this pilot single-centre study was to assess whether circulating histone levels could be used for diagnostic purposes in patients with AF. Methods: A total of 40 patients, well characterised for their biochemical and clinical characteristics, were recruited from outpatient clinics. Patients were randomly recruited into two groups (n = 20 per group), i.e., persistent AF and hypertensive controls. A multi-channel flow imaging methodology based on ImageStreamX was used with a well-optimised protocol to image and quantify five individual histones (H2A, H2B, H3, H4, and macroH2A1.1) together with the dimers (H2A/H2B, and H3/H4). Results: In the AF groups, plasma levels of histone dimers H2A/H2B and H3/H4 were elevated compared to hypertensive controls, 1.8% vs. 1.06% (p-value = 0.03). H2A/H2B dimer levels were increased in AF patients irrespective of gender, smoking status, diabetes, and pharmacological therapy. In the overall population, an inverse correlation between H2A and BMI was detected. Conclusions: Our pilot study, although limited in sample size, suggests that circulating histone complexes may be epigenetic sentinels for AF, offering mechanistic insights while addressing unmet needs in risk stratification.

## Linked entities

- **Proteins:** H2AC18 (H2A clustered histone 18), H2BC21 (H2B clustered histone 21), RLN3 (relaxin 3), CCDC6 (coiled-coil domain containing 6), MACROH2A1 (macroH2A.1 histone)
- **Diseases:** atrial fibrillation (MONDO:0004981), stroke (MONDO:0005098), diabetes (MONDO:0005015)

## Full-text entities

- **Genes:** NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, MACROH2A1 (macroH2A.1 histone) [NCBI Gene 9555] {aka H2A.y, H2A/y, H2AF12M, H2AFY, MACROH2A1.1, mH2A1}, HDAC9 (histone deacetylase 9) [NCBI Gene 9734] {aka HD7, HD7b, HD9, HDAC, HDAC7B, HDAC9B}, H2BC21 (H2B clustered histone 21) [NCBI Gene 8349] {aka GL105, H2B, H2B-GL105, H2B.1, H2BE, H2BFQ}, H2AC18 (H2A clustered histone 18) [NCBI Gene 8337] {aka H2A, H2A.2, H2A/O, H2A/q, H2AFO, H2a-615}
- **Diseases:** atrial remodelling (MESH:D064752), ACS (MESH:D054058), injury to (MESH:D014947), inflammation (MESH:D007249), fibrosis (MESH:D005355), non-alcoholic fatty liver disease (MESH:D065626), diabetes (MESH:D003920), cancer (MESH:D009369), myocardial injury (MESH:D009202), stroke (MESH:D020521), hepatic steatosis (MESH:D005234), inflammatory or autoimmune disease (MESH:D001327), arrhythmia (MESH:D001145), obese (MESH:D009765), thromboinflammation (MESH:D000090882), hypertension (MESH:D006973), cytotoxic (MESH:D064420), insulin resistance (MESH:D007333), myocardial infarction (MESH:D009203), coagulation (MESH:D001778), cardiovascular pathologies (MESH:D002318), AF (MESH:D001281), thromboembolism (MESH:D013923), dementia (MESH:D003704), type 2 diabetes (MESH:D003924), heart failure (MESH:D006333), sepsis (MESH:D018805), haemophilia (MESH:D006467), myocardial necrosis (MESH:D009336)
- **Chemicals:** Biofluids (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12922129/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12922129/full.md

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Source: https://tomesphere.com/paper/PMC12922129