Key result
Sacubitril/valsartan linked to ~6-point increase in LVEF over 12 months.
Why the study?
The study aimed to identify differences between aliskiren and sacubitril/valsartan in their effects on cardiac remodelling, metabolic balance, neurohumoral activation, and symptom severity in chronic heart failure.
How does sacubitril/valsartan compare with aliskiren in influencing cardiac remodelling, metabolic balance, neurohumoral activation, and clinical symptom severity in patients with chronic heart failure?
Observational
How does sacubitril/valsartan compare with aliskiren in influencing cardiac remodelling, metabolic balance, neurohumoral activation, and clinical symptom severity in patients with chronic heart failure?
Answers are grounded in this paper and cite their sources.
Sacubitril/valsartan provides rapid clinical stabilization and early LVEF improvement by 6 months, whereas aliskiren produces slower but pronounced structural reverse remodelling and pulmonary pressure reduction at 12 months in chronic heart failure.
The aim of the study was to identify differences between aliskiren and sacubitril/valsartan in their ability to influence cardiac remodelling, metabolic balance, neurohumoral activation, and clinical symptom severity. A comparative assessment of the clinical effectiveness and impact on the structural and functional state of the myocardium was conducted for two therapeutic strategies in patients with chronic heart failure in Georgia over a 12-month follow-up. The results demonstrated fundamentally different trajectories of therapeutic response. In the sacubitril/valsartan group, early clinical improvement was observed by 6 months, including significant reductions in systolic blood pressure (-6.2%, p<0.001), respiratory rate (-4.5%, p<0.001), and N-terminal pro-B-type natriuretic peptide levels (-10.0%, p<0.05), along with improved oxygen saturation (+3.5%, p<0.001). Left ventricular ejection fraction increased significantly already at 6 months (from 34.2±4.7% to 37.4±4.0%, p<0.001) and further at 12 months (40.5±3.5%, p<0.001), accompanied by rapid improvement in New York Heart Association functional class, with 9.3% of patients achieving New York Heart Association I by study end. In contrast, the aliskiren group exhibited slower but more pronounced structural reverse remodelling. Significant reductions in left ventricular end-systolic volume (-15.8%, p=0.009), end-diastolic volume (-17.6%, p=0.016), and end-systolic diameter (p=0.002) were observed only at 12 months, along with a modest but significant increase in ejection fraction (p=0.030). Regression of functional mitral and tricuspid regurgitation and a significant decrease in pulmonary artery systolic pressure (-19.7%, p<0.05) were more prominent in this group. Both therapies led to significant improvements in carbohydrate and lipid metabolism, including reductions in glycated haemoglobin, low-density lipoprotein cholesterol, and triglycerides (p<0.05 for all), indicating a favourable systemic metabolic effect. Overall, findings suggest that sacubitril/valsartan may be preferable when rapid clinical stabilization is required, whereas aliskiren may represent an effective therapeutic option for patients with advanced structural cardiac remodelling.
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TABUKASHVILI et al. (2026) conducted an observational in Chronic heart failure. Sacubitril/valsartan vs. Aliskiren was evaluated on Left ventricular ejection fraction (LVEF) and structural cardiac remodelling over 12 months (p=<0.001). Sacubitril/valsartan significantly increased left ventricular ejection fraction from 34.2% to 40.5% (p<0.001) over 12 months with early clinical stabilization by 6 months.
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