The Neutrophil–Lymphocyte Ratio Is Associated with Cardiac Magnetic Resonance Imaging-Derived Myocardial Fibrosis
<b>Background</b>: Sub-clinical inflammation is considered a key mechanism in cardiovascular disease and myocardial remodeling. We therefore evaluated whether the neutrophil-lymphocyte ratio (NLR), a simple inflammatory marker derived from a routine full blood count, is associated with myocardial fibrosis. <b>Methods</b>: Consecutive patients from a cardiac magnetic resonance imaging (CMR) registry were included and stratified by the NLR tertile. The association of the NLR and the levels of C-reactive protein (CRP) with CMR-derived myocardial T1 time and the extracellular volume fraction (ECV) were assessed using linear regression analysis and compared using Z-scores. In addition, an association with outcome was tested utilizing the log-rank test. <b>Results</b>: 1152 patients (72.4 years, 53.1% male) constituted the final cohort. The median NLR was 3.11 [interquartile range (IQR): 2.145-4.67]. Tertiles were based on the cut-off values ≤ 2.5, >2.5 and <4.0, and ≥4.0. A higher NLR tertile was associated with lower biventricular ejection fraction, hypertrophy, and increased right ventricular volume. The myocardial native T1 time [tertile 1 vs. 3: 1010 ms (984-1038) vs. 1030 (1001-1059), <i>p</i> < 0.001] and ECV [tertile 1 vs. 3: 26.3% (24.2-28.6) vs. 28.1% (25.5-31.4), <i>p</i> < 0.001] also significantly differed between the NLR tertiles. The NLR's and the CRP's association with elevated myocardial T1 time and ECV were comparable; however, the proportion of variation in the target variables explained by either was generally low. <b>Conclusions</b>: In our CMR all-comer cohort, NLR and CRP were significantly associated with prolonged myocardial T1 times and increased ECV. However, only a modest variation observed in both parameters was explained by either variable.
Authors
- Christian Loewe (ORCID: https://orcid.org/0000-0003-2502-0676)
- Dietrich Beitzke (ORCID: https://orcid.org/0000-0003-3179-3827)
- Carolina Donà (ORCID: https://orcid.org/0000-0002-6723-005X)
- Christian Nitsche (ORCID: https://orcid.org/0000-0002-0141-7639)
- Katharina Mascherbauer (ORCID: https://orcid.org/0000-0001-9681-1833)
- Michael Poledniczek (ORCID: https://orcid.org/0000-0002-6091-9823)
- Matthias Koschutnik (ORCID: https://orcid.org/0000-0001-6164-8773)
- Christina Kronberger (ORCID: https://orcid.org/0000-0002-3866-3710)
- Andreas Anselm Kammerlander (ORCID: https://orcid.org/0000-0002-7632-9879)
- Laura Lunzer
- Lena Marie Schmid
- Christian Hengstenberg
Institutions
- Medical University of Vienna (AT)
Publication Details
- Journal
- Journal of Clinical Medicine
- Published
- 2026-02-12
- DOI
- https://doi.org/10.3390/jcm15041441
- Primary Topic
- Inflammatory Biomarkers in Disease Prognosis
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Universität Wien
- Medizinische Universität Wien
- Österreichische Kardiologische Gesellschaft