Key result
Sacubitril/valsartan is linked to ~69% lower risk of cognitive decline at 6 months vs control.
Why the study?
Cognitive decline during ischemic stroke recovery in patients with AF is associated with LVEF ≤ 48 %, prompting investigation into cognitive changes with sacubitril/valsartan.
Does sacubitril/valsartan reduce cognitive decline in patients with nonvalvular atrial fibrillation, LVEF ≤ 48%, and recent ischemic stroke?
Cohort (n=53)
Does sacubitril/valsartan reduce cognitive decline in patients with nonvalvular atrial fibrillation, LVEF ≤ 48%, and recent ischemic stroke?
In patients with atrial fibrillation, reduced LVEF, and recent ischemic stroke, sacubitril/valsartan administration may reduce the risk of cognitive decline and improve LVEF.
Answers are grounded in this paper and cite their sources.
Associated with lower cognitive decline risk in AF with reduced LVEF post-stroke; leaves open causal benefit pending randomized trials.
Background. Cognitive decline (CD) during the recovery period of ischemic strokes in patients with atrial fibrillation (AF) is associated with left ventricular ejection fraction (LVEF) ≤ 48 %. Objective: to investigate cognitive changes during the recovery period of ischemic strokes in patients with AF and LVEF ≤ 48 % who took sacubitril/valsartan. Materials and methods. Patients with nonvalvular AF and LVEF ≤ 48 % who had an ischemic non-lacunar stroke within the last 6 months were examined. Thirty-nine people in the control group received protocol treatment, and 14 patients additionally took sacubitril/valsartan 100 mg twice daily for 6 months. Cognitive and echocardiographic parameters were assessed at the first examination and after 6 months. CD was diagnosed when the cognitive scores decreased by ≥ 1 point. Results. Both groups of patients at the time of inclusion did not differ significantly in cognitive functioning, socio-demographic, clinical, psycho-emotional characteristics, and echocardiographic parameters. Six-month administration of sacubitril/valsartan was associated with a significant reduction in the relative risk of CD on all used cognitive scales compared to the control group: by 3.18 times (95% confidence interval (CI) 1.42–7.16) on the Montreal Cognitive Assessment, by 2.79 times (95% CI 1.29–6.00) on the Clock Drawing Test and by 2.48 times (95% CI 1.19–5.14) on the Mini-Mental State Examination and the Frontal Assessment Battery. In addition, the sacubitril/valsartan intake was associated with a reliable increase in LVEF compared to baseline (40.3 (38.1–42.4) vs. 40.1 (39.4–42.5) %); in contrast, in the control group, no such pattern was observed. Conclusions. In patients with AF and LVEF ≤ 48 %, sacubitril/valsartan administration in the recovery period of ischemic non-lacunar stroke is associated with a significant improvement in cognitive functioning.
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Delva et al. (2025) conducted a cohort in Ischemic non-lacunar stroke in patients with atrial fibrillation and LVEF ≤ 48% (n=53). Sacubitril/valsartan vs. Protocol treatment was evaluated on Cognitive decline (decrease in cognitive scores by ≥ 1 point) (RR 3.18, 95% CI 1.42-7.16). Sacubitril/valsartan administration for 6 months reduced the relative risk of cognitive decline on the Montreal Cognitive Assessment by 3.18 times (95% CI 1.42-7.16) compared to control.
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