Evidence map›Paper›PMID 40120053›Full record

ArticleMolecular and cellular biochemistry2025

Histone H2A: a promising diagnostic marker in heart failure with reduced versus preserved ejection fraction.

Desislava K Tsoneva, Diana Buzova, Salvatore Daniele Bianco, Antoniya Kisheva, Mesut Rushid, Tanya Ivanova, Yoto Yotov, Jan Cerveny, Tommaso Mazza, Manlio Vinciguerra

Abstract read
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In one paragraph

Article in Molecular and cellular biochemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Article
  2. Nuclear Proteome Map of Mouse Heart Chambers.Molecular & cellular proteomics : MCP · 2026
    Article
  3. Review
  4. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Desislava K Tsoneva *Department of Medical Genetics, Medical University of Varna, Varna, Bulgaria.
Diana Buzova *Department of Adaptive Biotechnologies, Global Change Research Institute CAS, Brno, Czech Republic.
Salvatore Daniele BiancoBioinformatics Laboratory, Fondazione IRCCS Casa Sollievo Della Sofferenza, S. Giovanni Rotondo (FG), Italy.
Antoniya KishevaFaculty of Medicine, First Department of Internal Diseases, Medical University of Varna, Varna, Bulgaria.
Mesut RushidFaculty of Medicine, First Department of Internal Diseases, Medical University of Varna, Varna, Bulgaria.
Tanya IvanovaFaculty of Medicine, First Department of Internal Diseases, Medical University of Varna, Varna, Bulgaria.
Yoto YotovFaculty of Medicine, First Department of Internal Diseases, Medical University of Varna, Varna, Bulgaria.
Jan CervenyDepartment of Adaptive Biotechnologies, Global Change Research Institute CAS, Brno, Czech Republic.
Tommaso MazzaComputational Biology and Bioinformatics Unit, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Roma, Italy. tommaso.mazza@policlinicogemelli.it.
Manlio VinciguerraDepartment of Stem Cell Biology and Transplantology, Research Institute of the Medical University of Varna, Varna, Bulgaria. manlio.vinciguerra@mu-varna.bg.

Funding

Ministry of Education and Science of Bulgaria under the National Scientific Programme "Excellent Research and People for the Development of European Science" 2021 (VIHREN) of the Bulgarian National Science Fund contract #KP-06-DV/4 from 15.12.2021
6 · The paper itself

Abstract

The diagnosis of heart failure with preserved left ventricle ejection fraction (HFpEF) remains a challenge, with score-based algorithms showing varying diagnostic performance and biomarkers sometimes inconclusive. This study aimed to examine whether circulating histones and histone complexes, which recently emerged as robust biomarkers of inflammation and stroke, show distinct profiles in plasma from healthy individuals, HF with reduced EF (HFrEF), and HFpEF patients. We evaluated the plasma histone profile of 30 sex/age-matched healthy individuals, 22 HFpEF and 25 HFrEF prior any therapeutic intervention. ImageStreamX-based detection approach was used to measure the levels of circulating particles positive for core histones H2A, H2B, H3, H4, histone variants macroH2A1.1 and macroH2A1.2. While we found increased levels of most of the histones and histone complexes in both HFpEF and HFrEF patients, H2A was significantly elevated only in HFpEF, compared to healthy individuals (p-value = 0.002) and to HFrEF (p-value = 0.00008). In line with these findings, H2A showed positive correlation with EF (r = 0.493). We identified a plasma histone profile able to detect HF and differentiate between HFpEF and HFrEF using a high throughput and imaging flow cytometry-adapted liquid biopsy.

Indexed as

Heart FailureHistonesStroke VolumeAgedBiomarkersFemaleHumansMaleMiddle AgedBiomarkersHistonesHeart failureHistonesLiquid biopsyPlasmaPreserved ejection fractionReduced ejection fraction

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.