There is strong evidence that inflammatory mediators play a key role in the progression to
heart failure in patients with systemic
hypertension (HTN). The present study aimed to identify a set of
cytokines that are associated with early left ventricular (LV) remodeling and dysfunction as captured by echocardiography in patients with HTN in a cross-sectional case-control study nested within the FLEMish study on ENvironment, Genes and Health Outcome. We identified three groups of participants from the cohort: normotensive subjects (normotension;
n = 30), HTN with normal LV structure and function (HTN [LV-];
n = 30), and HTN with evidence of adverse LV remodeling (HTN [LV+]; n = 50). We measured
cytokines using a 63-plex Luminex platform. Using partial least squares-discriminant analysis, we constructed three latent variables from the measured
cytokines that explained 35%-45% of the variance between groups. We identified five common
cytokines (
interleukin 18, monokine induced by
gamma interferon,
hepatocyte growth factor, epithelial neutrophil-activating
peptide 78, and
vascular endothelial growth factor D) with a stable signal which had a major impact on the construction of the latent variables. Among these
cytokines, after adjustment for confounders,
interleukin 18 remained significantly different between HTN participants with and without LV involvement (P = .02). Moreover,
granulocyte-macrophage colony-stimulating factor and
leptin showed a consistent upward trend in all HTN patients compared with normotensive subjects. In conclusion, in HTN patients with LV remodeling or/and dysfunction, we identified a set of
cytokines strongly associated with LV maladaptation. We also found a distinct profile of inflammatory
biomarkers that characterize HTN.