Evidence map›Paper›PMID 40024803›Full record

ArticleESC heart failure2025

Neutrophil-to-lymphocyte ratio: link to congestion, inflammation, and mortality in outpatients with heart failure.

Asma O M Rezig, Moustafa I Morsy, Elisabetta Caiazzo, Antonio Iaconelli, Armando Ialenti, David Hunter, Joe J Cuthbert, Syed Kazmi, Tomasz J Guzik, Dario Bruzzese and 4 more

Abstract read
In one paragraph

Article in ESC heart failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
–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

9 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Metabolic-inflammatory burden predicts mortality in heart failure across population and ICU cohorts.International journal of cardiology. Cardiovascular risk and prevention · 2026
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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

14 authors.

Asma O M RezigSchool of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Moustafa I MorsySchool of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.ORCID https://orcid.org/0000-0001-9878-8913
Elisabetta CaiazzoSchool of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Antonio IaconelliSchool of Cardiovascular and Metabolic Health, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Armando IalentiDepartment of Pharmacy, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
David HunterSchool of Cardiovascular and Metabolic Health, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Joe J CuthbertDepartment of Cardiorespiratory Medicine, Centre for Clinical Sciences, Hull York Medical School, University of Hull, Kingston Upon Hull, UK.
Syed KazmiDepartment of Cardiorespiratory Medicine, Centre for Clinical Sciences, Hull York Medical School, University of Hull, Kingston Upon Hull, UK.
Tomasz J GuzikCentre for Cardiovascular Science, Queen's Medical Research Institute, University of Edinburgh, Edinburgh, UK.
Dario BruzzeseDepartment of Public Health, School of Medicine and Surgery, University of Naples Federico II, Naples, Italy.
John G F ClelandSchool of Cardiovascular and Metabolic Health, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Andrew L ClarkDepartment of Cardiology, Castle Hill Hospital, Hull University Teaching Hospitals Trust, Kingston Upon Hull, UK.
Pasquale MaffiaSchool of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
Pierpaolo PellicoriSchool of Cardiovascular and Metabolic Health, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.

Funding

British Heart Foundation FS/19/56/34893ABritish Heart Foundation PG/19/84/34771British Heart Foundation PG/21/10541British Heart Foundation PG/21/10557British Heart Foundation PG/21/10634British Heart Foundation PG/23/11680British Heart Foundation PG/24/11946British Heart Foundation Centre of Research Excellence FS/14/49/30838British Heart Foundation Centre of Research Excellence FS/4yPhD/F/20/34127ABritish Heart Foundation Centre of Research Excellence RE/18/5/34216British Heart Foundation Centre of Research Excellence RE/18/6134217European Research Area-CVD (ERA-CVD)European Research Council ERC-CoG-726318European Union-Next Generation EU CUP B93D21010860004Fondazione Enrico ed Enrica SovenaHeart Research UK RG2676/18/21Italian Ministry of University and Research 2017NKB2N4_003University of Glasgow and the International Science Partnership FundUniversity of Naples Federico II/Compagnia di San Paolo and the Italian Ministry of University and Research (MUR) 2022T45AXH
6 · The paper itself

Abstract

backgroundThe neutrophil-to-lymphocyte ratio (NLR) may be a useful marker of inflammation, but its associations with clinical characteristics, signs of congestion and outcome in patients with chronic heart failure (HF) are unknown. METHODS AND

resultsWe enrolled 4702 ambulatory patients with HF and either left ventricular systolic dysfunction or high N-terminal pro-B-type natriuretic peptide (NTproBNP) (≥125 ng/L). Compared with those in the lowest quartile of NLR (≤2.05), patients in the highest quartile (≥4.10) were older, had higher NTproBNP, and were more likely to have HF with reduced left ventricular ejection fraction (HFrEF), atrial fibrillation and to be treated with loop diuretics. In 813 patients with detailed echocardiographic assessment, lymphocyte count correlated inversely with NTproBNP (r = -0.31) and markers of congestion [left atrial volume index (r = -0.25), inferior vena cava diameter (r = -0.24)]; neutrophil count correlated positively with high-sensitivity C-reactive protein (hsCRP) (r = 0.31, P < 0.001). During a median follow-up of 54 (29-100) months, 3015 (64%) patients died. In models adjusted for NTproBNP and HsCRP, higher NLR [hazard ratio (HR):1.05; 95% confidence interval (CI) 1.03-1.06] and neutrophil count (HR:1.07; 95%CI 1.04-1.10) were associated with higher mortality rates; higher lymphocyte count (HR:0.88; 95%CI 0.82-0.95) was associated with lower risk (all P < 0.001).

conclusionsLow lymphocyte count is associated with more congestion and high neutrophil count with more inflammation, which may explain why a greater NLR is associated with a poorer prognosis. For patients with heart failure, NLR or its components could be useful for risk stratification or for monitoring evolving risk, but might also be therapeutic targets.

Indexed as

Heart FailureInflammationLymphocytesNeutrophilsOutpatientsAgedBiomarkersC-Reactive ProteinEchocardiographyFemaleFollow-Up StudiesHumansLeukocyte CountMaleMiddle AgedNatriuretic Peptide, BrainBiomarkersC-Reactive ProteinNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)chronic heart failurecongestioninflammationmortalityNLR

Identifiers

PMID40024803
PMCPMC12055385

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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 OpenQuestion graph.