Key result
Patients with LVH associated with HFpEF had a significantly lower Treg/Th-act ratio compared to those with asymptomatic hypertensive LVH (p = 0.001).
Why the study?
Chronic inflammation and fibrosis drive cardiac remodeling in LVH and HFpEF, but the relationship between circulating CD4+ T-cell and monocyte subpopulations and LV diastolic function across these conditions required evaluation.
Observational (n=57)
p-value: p=0.001
The transition from asymptomatic hypertensive LVH to HFpEF is associated with immune cell alterations, specifically a lower Treg/Th-act ratio and correlations between intermediate monocytes and diastolic dysfunction.
May link T-cell imbalance to HFpEF progression in LVH; hypothesis-generating and requires prospective confirmation before clinical consideration.
(1) Background: Chronic inflammation and fibrosis are key players in cardiac remodeling associated with left ventricular hypertrophy (LVH) and heart failure with a preserved ejection fraction (HFpEF). Monocytes and T-helpers (Th) are involved in both pro-inflammatory and fibrotic processes, while regulatory T-cells (Treg) could be considered to suppress chronic inflammation in the hypertrophied myocardium. We aimed to estimate the relationship between the frequencies of circulating CD4+ T-cell and monocyte subpopulations and the variables of left ventricular (LV) diastolic function in patients with LVH depending on the presence of HFpEF. (2) Methods: We enrolled 57 patients with asymptomatic hypertensive LVH (n = 21), or LVH associated with HFpEF (n = 36). A clinical assessment and echocardiographs were analyzed. CD4+ Treg, activated Th (Th-act), and monocyte (classical, intermediate, and non-classical) subpopulations were evaluated via direct immunofluorescence and flow cytometry. (3) Results: Patients with HFpEF had a lower Treg/Th-act ratio (p = 0.001). Though asymptomatic patients and patients with HFpEF were comparable in terms of both the total monocyte number and monocyte subsets, there were moderate correlations between intermediate monocyte count and conventional and novel echocardiographic variables of LV diastolic dysfunction in patients with HFpEF. (4) Conclusions: In patients with LVH, the clinical deterioration (transition to HFpEF) and progression of LV diastolic dysfunction are probably associated with T-cell disbalance and an increase in intermediate monocyte counts.
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Овчинников et al. (2023) conducted an observational in Hypertensive left ventricular hypertrophy and heart failure with preserved ejection fraction (n=57). Heart failure with preserved ejection fraction (HFpEF) vs. Asymptomatic hypertensive LVH was evaluated on Treg/Th-act ratio (p=0.001). Patients with LVH associated with HFpEF had a significantly lower Treg/Th-act ratio compared to those with asymptomatic hypertensive LVH (p = 0.001).
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